Other Cell Processes - MCAT Biological and Biochemical Foundations of Living Systems
Card 0 of 56
Apoptosis can be induced by mitochondria via the release of which protein from the mitochondrial inner membrane?
Apoptosis can be induced by mitochondria via the release of which protein from the mitochondrial inner membrane?
During the intrinsic cycle of apoptosis, the mitochondrial outer membrane becomes permeable to cytochrome C. The release of cytochrome C induces multiple cellular processes that lead to apoptosis.
During the intrinsic cycle of apoptosis, the mitochondrial outer membrane becomes permeable to cytochrome C. The release of cytochrome C induces multiple cellular processes that lead to apoptosis.
Compare your answer with the correct one above
The mechanism by which a macrophage engulfs cellular debris and/or pathogens is best described as
.
The mechanism by which a macrophage engulfs cellular debris and/or pathogens is best described as .
Macrophages are immune cells that phagocytize cell debris and pathogens, then fuse with lysosomes to digest the material. Receptor-mediated endocytosis is a form of endocytosis primarily involved in viral infection or protein uptake. Pinocytosis refers to the uptake of liquid, specifically, from the extracellular medium. Exocytosis is the opposite of what is being described in this question.
Macrophages are immune cells that phagocytize cell debris and pathogens, then fuse with lysosomes to digest the material. Receptor-mediated endocytosis is a form of endocytosis primarily involved in viral infection or protein uptake. Pinocytosis refers to the uptake of liquid, specifically, from the extracellular medium. Exocytosis is the opposite of what is being described in this question.
Compare your answer with the correct one above
Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A novel cell line is created that lacks PrPC. These cells are functionally normal except they grow uncontrollably and do not appear to have a finite number of divisions. PrPC is thus most likely involved in which process?
Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A novel cell line is created that lacks PrPC. These cells are functionally normal except they grow uncontrollably and do not appear to have a finite number of divisions. PrPC is thus most likely involved in which process?
Apoptosis is programmed cell death. If cells are growing uncontrollably without a natural end to their growth patterns, they are likely not undergoing apoptosis.
Apoptosis is programmed cell death. If cells are growing uncontrollably without a natural end to their growth patterns, they are likely not undergoing apoptosis.
Compare your answer with the correct one above
Most scientists subscribe to the theory of endosymbiosis to explain the presence of mitochondria in eukaryotic cells. According to the theory of endosymbiosis, early pre-eukaryotic cells phagocytosed free living prokaryotes, but failed to digest them. As a result, these prokaryotes remained in residence in the pre-eukaryotes, and continued to generate energy. The host cells were able to use this energy to gain a selective advantage over their competitors, and eventually the energy-producing prokaryotes became mitochondria.
In many ways, mitochondria are different from other cellular organelles, and these differences puzzled scientists for many years. The theory of endosymbiosis concisely explains a number of these observations about mitochondria. Perhaps most of all, the theory explains why aerobic metabolism is entirely limited to this one organelle, while other kinds of metabolism are more distributed in the cellular cytosol.
Cells with abnormalities in critical systems, such as mitochondria, will often undergo apoptosis. Which of the following is true of apoptosis?
Most scientists subscribe to the theory of endosymbiosis to explain the presence of mitochondria in eukaryotic cells. According to the theory of endosymbiosis, early pre-eukaryotic cells phagocytosed free living prokaryotes, but failed to digest them. As a result, these prokaryotes remained in residence in the pre-eukaryotes, and continued to generate energy. The host cells were able to use this energy to gain a selective advantage over their competitors, and eventually the energy-producing prokaryotes became mitochondria.
In many ways, mitochondria are different from other cellular organelles, and these differences puzzled scientists for many years. The theory of endosymbiosis concisely explains a number of these observations about mitochondria. Perhaps most of all, the theory explains why aerobic metabolism is entirely limited to this one organelle, while other kinds of metabolism are more distributed in the cellular cytosol.
Cells with abnormalities in critical systems, such as mitochondria, will often undergo apoptosis. Which of the following is true of apoptosis?
Apoptosis and necrosis are distinct processes. Apoptosis is a biologically healthy death of cells, self-limiting and helpful in the elimination of abnormal cells. Necrosis is a pathological state of cell death, and drives inflammation.
Apoptosis and necrosis are distinct processes. Apoptosis is a biologically healthy death of cells, self-limiting and helpful in the elimination of abnormal cells. Necrosis is a pathological state of cell death, and drives inflammation.
Compare your answer with the correct one above
Which cells would be expected to have the highest rate of endocytosis?
Which cells would be expected to have the highest rate of endocytosis?
Endocytosis is the uptake of extracellular materials in vesicles. After release of neurotransmitter into the synaptic cleft, neurons are able to re-uptake the neurotransmitter via endocytosis. This allows them to recycle the cell membrane and molecular components that are released during an action potential.
Erythrocytes are red blood cells, osteoblasts are bone-producing cells, and B-cells are responsible for producing antibodies. None of these cell types plays a significant role in particulate uptake. One should note, however, that while B-cells do not frequently use endocytosis, cytotoxic T-cells are able to phagocytose cellular debris through endocytosis.
Endocytosis is the uptake of extracellular materials in vesicles. After release of neurotransmitter into the synaptic cleft, neurons are able to re-uptake the neurotransmitter via endocytosis. This allows them to recycle the cell membrane and molecular components that are released during an action potential.
Erythrocytes are red blood cells, osteoblasts are bone-producing cells, and B-cells are responsible for producing antibodies. None of these cell types plays a significant role in particulate uptake. One should note, however, that while B-cells do not frequently use endocytosis, cytotoxic T-cells are able to phagocytose cellular debris through endocytosis.
Compare your answer with the correct one above
Which of the following are common occurances in apoptosis that are not seen during necrosis?
I. Membrane blebbing
II. DNA fragmentation
III. Cell shrinkage
Which of the following are common occurances in apoptosis that are not seen during necrosis?
I. Membrane blebbing
II. DNA fragmentation
III. Cell shrinkage
Apoptosis is a highly organized system of programmed cell death. Necrosis is premature cell death, typically caused by outside forces. In apoptosis membrane blebbing and bulging is observed, but the membrane itself maintains its integrity. In necrosis the membrane is usually disrupted. In both apoptosis and necrosis there is DNA fragmentation. Apoptosis is unique, however, in the fact that it has organized DNA fragmentation (during necrosis it is random). Apoptotic cells typically shrink, while necrotic cells swell.
Apoptosis is a highly organized system of programmed cell death. Necrosis is premature cell death, typically caused by outside forces. In apoptosis membrane blebbing and bulging is observed, but the membrane itself maintains its integrity. In necrosis the membrane is usually disrupted. In both apoptosis and necrosis there is DNA fragmentation. Apoptosis is unique, however, in the fact that it has organized DNA fragmentation (during necrosis it is random). Apoptotic cells typically shrink, while necrotic cells swell.
Compare your answer with the correct one above
There are two models for the operation of the Golgi apparatus in eukaryotic cells. As it is difficult to visualize the operation of cells at the molecular level in real time, scientists typically rely on static electron micrographs to see the morphology of organelles. As a result, the dynamic operation of these organelles can sometimes be unclear.
Cisternal Maturation Hypothesis
In the cisternal maturation hypothesis, the cisternae of the Golgi apparatus evolve. Proteins leave the endoplasmic reticulum, and enter the cis-Golgi. The cisterna of the cis-Golgi then matures, with its enzymatic contents and internal environment changing as it becomes the medial-Golgi, and, eventually, the trans-Golgi.
In this model, the proteins never physically leave their membrane-bound cisternae during their transit across the Golgi. Instead, the entire unit of contents remains within the evolving cisternae.
Vesicular Transport Hypothesis
In contrast to the cisternal maturation hypothesis, the vesicular transport hypothesis posits that the cis-, medial-, and trans-Golgi cisternae are more static structures. Instead of evolving around their contents, the contents are physically shuttled via vesicular intermediates from each cisterna to the next.
In the case of vesicular transport, vesicles are shuttled along microtubules. Motor proteins facilitate this movement, with unique proteins being used for each direction of movement along a microtubule.
The Golgi apparatus has been implicated in cell death pathways. A scientist finds that a cell death pathway involving the Golgi is used in the breakdown of extra skin between digits during embryonic development. This pathway
.
There are two models for the operation of the Golgi apparatus in eukaryotic cells. As it is difficult to visualize the operation of cells at the molecular level in real time, scientists typically rely on static electron micrographs to see the morphology of organelles. As a result, the dynamic operation of these organelles can sometimes be unclear.
Cisternal Maturation Hypothesis
In the cisternal maturation hypothesis, the cisternae of the Golgi apparatus evolve. Proteins leave the endoplasmic reticulum, and enter the cis-Golgi. The cisterna of the cis-Golgi then matures, with its enzymatic contents and internal environment changing as it becomes the medial-Golgi, and, eventually, the trans-Golgi.
In this model, the proteins never physically leave their membrane-bound cisternae during their transit across the Golgi. Instead, the entire unit of contents remains within the evolving cisternae.
Vesicular Transport Hypothesis
In contrast to the cisternal maturation hypothesis, the vesicular transport hypothesis posits that the cis-, medial-, and trans-Golgi cisternae are more static structures. Instead of evolving around their contents, the contents are physically shuttled via vesicular intermediates from each cisterna to the next.
In the case of vesicular transport, vesicles are shuttled along microtubules. Motor proteins facilitate this movement, with unique proteins being used for each direction of movement along a microtubule.
The Golgi apparatus has been implicated in cell death pathways. A scientist finds that a cell death pathway involving the Golgi is used in the breakdown of extra skin between digits during embryonic development. This pathway .
Apoptosis is the normal, physiologic elimination of cells. These include cancer cells, skin cells as described in the question, and others. It mainly involves the release of sequestered enzymes and mediators from within an apoptotic cell, such as from the Golgi apparatus or lysosomes.
Apoptosis is the normal, physiologic elimination of cells. These include cancer cells, skin cells as described in the question, and others. It mainly involves the release of sequestered enzymes and mediators from within an apoptotic cell, such as from the Golgi apparatus or lysosomes.
Compare your answer with the correct one above
Apoptosis can be induced by mitochondria via the release of which protein from the mitochondrial inner membrane?
Apoptosis can be induced by mitochondria via the release of which protein from the mitochondrial inner membrane?
During the intrinsic cycle of apoptosis, the mitochondrial outer membrane becomes permeable to cytochrome C. The release of cytochrome C induces multiple cellular processes that lead to apoptosis.
During the intrinsic cycle of apoptosis, the mitochondrial outer membrane becomes permeable to cytochrome C. The release of cytochrome C induces multiple cellular processes that lead to apoptosis.
Compare your answer with the correct one above
Apoptosis can be induced by mitochondria via the release of which protein from the mitochondrial inner membrane?
Apoptosis can be induced by mitochondria via the release of which protein from the mitochondrial inner membrane?
During the intrinsic cycle of apoptosis, the mitochondrial outer membrane becomes permeable to cytochrome C. The release of cytochrome C induces multiple cellular processes that lead to apoptosis.
During the intrinsic cycle of apoptosis, the mitochondrial outer membrane becomes permeable to cytochrome C. The release of cytochrome C induces multiple cellular processes that lead to apoptosis.
Compare your answer with the correct one above
Apoptosis can be induced by mitochondria via the release of which protein from the mitochondrial inner membrane?
Apoptosis can be induced by mitochondria via the release of which protein from the mitochondrial inner membrane?
During the intrinsic cycle of apoptosis, the mitochondrial outer membrane becomes permeable to cytochrome C. The release of cytochrome C induces multiple cellular processes that lead to apoptosis.
During the intrinsic cycle of apoptosis, the mitochondrial outer membrane becomes permeable to cytochrome C. The release of cytochrome C induces multiple cellular processes that lead to apoptosis.
Compare your answer with the correct one above
The mechanism by which a macrophage engulfs cellular debris and/or pathogens is best described as
.
The mechanism by which a macrophage engulfs cellular debris and/or pathogens is best described as .
Macrophages are immune cells that phagocytize cell debris and pathogens, then fuse with lysosomes to digest the material. Receptor-mediated endocytosis is a form of endocytosis primarily involved in viral infection or protein uptake. Pinocytosis refers to the uptake of liquid, specifically, from the extracellular medium. Exocytosis is the opposite of what is being described in this question.
Macrophages are immune cells that phagocytize cell debris and pathogens, then fuse with lysosomes to digest the material. Receptor-mediated endocytosis is a form of endocytosis primarily involved in viral infection or protein uptake. Pinocytosis refers to the uptake of liquid, specifically, from the extracellular medium. Exocytosis is the opposite of what is being described in this question.
Compare your answer with the correct one above
Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A novel cell line is created that lacks PrPC. These cells are functionally normal except they grow uncontrollably and do not appear to have a finite number of divisions. PrPC is thus most likely involved in which process?
Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A novel cell line is created that lacks PrPC. These cells are functionally normal except they grow uncontrollably and do not appear to have a finite number of divisions. PrPC is thus most likely involved in which process?
Apoptosis is programmed cell death. If cells are growing uncontrollably without a natural end to their growth patterns, they are likely not undergoing apoptosis.
Apoptosis is programmed cell death. If cells are growing uncontrollably without a natural end to their growth patterns, they are likely not undergoing apoptosis.
Compare your answer with the correct one above
Most scientists subscribe to the theory of endosymbiosis to explain the presence of mitochondria in eukaryotic cells. According to the theory of endosymbiosis, early pre-eukaryotic cells phagocytosed free living prokaryotes, but failed to digest them. As a result, these prokaryotes remained in residence in the pre-eukaryotes, and continued to generate energy. The host cells were able to use this energy to gain a selective advantage over their competitors, and eventually the energy-producing prokaryotes became mitochondria.
In many ways, mitochondria are different from other cellular organelles, and these differences puzzled scientists for many years. The theory of endosymbiosis concisely explains a number of these observations about mitochondria. Perhaps most of all, the theory explains why aerobic metabolism is entirely limited to this one organelle, while other kinds of metabolism are more distributed in the cellular cytosol.
Cells with abnormalities in critical systems, such as mitochondria, will often undergo apoptosis. Which of the following is true of apoptosis?
Most scientists subscribe to the theory of endosymbiosis to explain the presence of mitochondria in eukaryotic cells. According to the theory of endosymbiosis, early pre-eukaryotic cells phagocytosed free living prokaryotes, but failed to digest them. As a result, these prokaryotes remained in residence in the pre-eukaryotes, and continued to generate energy. The host cells were able to use this energy to gain a selective advantage over their competitors, and eventually the energy-producing prokaryotes became mitochondria.
In many ways, mitochondria are different from other cellular organelles, and these differences puzzled scientists for many years. The theory of endosymbiosis concisely explains a number of these observations about mitochondria. Perhaps most of all, the theory explains why aerobic metabolism is entirely limited to this one organelle, while other kinds of metabolism are more distributed in the cellular cytosol.
Cells with abnormalities in critical systems, such as mitochondria, will often undergo apoptosis. Which of the following is true of apoptosis?
Apoptosis and necrosis are distinct processes. Apoptosis is a biologically healthy death of cells, self-limiting and helpful in the elimination of abnormal cells. Necrosis is a pathological state of cell death, and drives inflammation.
Apoptosis and necrosis are distinct processes. Apoptosis is a biologically healthy death of cells, self-limiting and helpful in the elimination of abnormal cells. Necrosis is a pathological state of cell death, and drives inflammation.
Compare your answer with the correct one above
Which cells would be expected to have the highest rate of endocytosis?
Which cells would be expected to have the highest rate of endocytosis?
Endocytosis is the uptake of extracellular materials in vesicles. After release of neurotransmitter into the synaptic cleft, neurons are able to re-uptake the neurotransmitter via endocytosis. This allows them to recycle the cell membrane and molecular components that are released during an action potential.
Erythrocytes are red blood cells, osteoblasts are bone-producing cells, and B-cells are responsible for producing antibodies. None of these cell types plays a significant role in particulate uptake. One should note, however, that while B-cells do not frequently use endocytosis, cytotoxic T-cells are able to phagocytose cellular debris through endocytosis.
Endocytosis is the uptake of extracellular materials in vesicles. After release of neurotransmitter into the synaptic cleft, neurons are able to re-uptake the neurotransmitter via endocytosis. This allows them to recycle the cell membrane and molecular components that are released during an action potential.
Erythrocytes are red blood cells, osteoblasts are bone-producing cells, and B-cells are responsible for producing antibodies. None of these cell types plays a significant role in particulate uptake. One should note, however, that while B-cells do not frequently use endocytosis, cytotoxic T-cells are able to phagocytose cellular debris through endocytosis.
Compare your answer with the correct one above
Which of the following are common occurances in apoptosis that are not seen during necrosis?
I. Membrane blebbing
II. DNA fragmentation
III. Cell shrinkage
Which of the following are common occurances in apoptosis that are not seen during necrosis?
I. Membrane blebbing
II. DNA fragmentation
III. Cell shrinkage
Apoptosis is a highly organized system of programmed cell death. Necrosis is premature cell death, typically caused by outside forces. In apoptosis membrane blebbing and bulging is observed, but the membrane itself maintains its integrity. In necrosis the membrane is usually disrupted. In both apoptosis and necrosis there is DNA fragmentation. Apoptosis is unique, however, in the fact that it has organized DNA fragmentation (during necrosis it is random). Apoptotic cells typically shrink, while necrotic cells swell.
Apoptosis is a highly organized system of programmed cell death. Necrosis is premature cell death, typically caused by outside forces. In apoptosis membrane blebbing and bulging is observed, but the membrane itself maintains its integrity. In necrosis the membrane is usually disrupted. In both apoptosis and necrosis there is DNA fragmentation. Apoptosis is unique, however, in the fact that it has organized DNA fragmentation (during necrosis it is random). Apoptotic cells typically shrink, while necrotic cells swell.
Compare your answer with the correct one above
There are two models for the operation of the Golgi apparatus in eukaryotic cells. As it is difficult to visualize the operation of cells at the molecular level in real time, scientists typically rely on static electron micrographs to see the morphology of organelles. As a result, the dynamic operation of these organelles can sometimes be unclear.
Cisternal Maturation Hypothesis
In the cisternal maturation hypothesis, the cisternae of the Golgi apparatus evolve. Proteins leave the endoplasmic reticulum, and enter the cis-Golgi. The cisterna of the cis-Golgi then matures, with its enzymatic contents and internal environment changing as it becomes the medial-Golgi, and, eventually, the trans-Golgi.
In this model, the proteins never physically leave their membrane-bound cisternae during their transit across the Golgi. Instead, the entire unit of contents remains within the evolving cisternae.
Vesicular Transport Hypothesis
In contrast to the cisternal maturation hypothesis, the vesicular transport hypothesis posits that the cis-, medial-, and trans-Golgi cisternae are more static structures. Instead of evolving around their contents, the contents are physically shuttled via vesicular intermediates from each cisterna to the next.
In the case of vesicular transport, vesicles are shuttled along microtubules. Motor proteins facilitate this movement, with unique proteins being used for each direction of movement along a microtubule.
The Golgi apparatus has been implicated in cell death pathways. A scientist finds that a cell death pathway involving the Golgi is used in the breakdown of extra skin between digits during embryonic development. This pathway
.
There are two models for the operation of the Golgi apparatus in eukaryotic cells. As it is difficult to visualize the operation of cells at the molecular level in real time, scientists typically rely on static electron micrographs to see the morphology of organelles. As a result, the dynamic operation of these organelles can sometimes be unclear.
Cisternal Maturation Hypothesis
In the cisternal maturation hypothesis, the cisternae of the Golgi apparatus evolve. Proteins leave the endoplasmic reticulum, and enter the cis-Golgi. The cisterna of the cis-Golgi then matures, with its enzymatic contents and internal environment changing as it becomes the medial-Golgi, and, eventually, the trans-Golgi.
In this model, the proteins never physically leave their membrane-bound cisternae during their transit across the Golgi. Instead, the entire unit of contents remains within the evolving cisternae.
Vesicular Transport Hypothesis
In contrast to the cisternal maturation hypothesis, the vesicular transport hypothesis posits that the cis-, medial-, and trans-Golgi cisternae are more static structures. Instead of evolving around their contents, the contents are physically shuttled via vesicular intermediates from each cisterna to the next.
In the case of vesicular transport, vesicles are shuttled along microtubules. Motor proteins facilitate this movement, with unique proteins being used for each direction of movement along a microtubule.
The Golgi apparatus has been implicated in cell death pathways. A scientist finds that a cell death pathway involving the Golgi is used in the breakdown of extra skin between digits during embryonic development. This pathway .
Apoptosis is the normal, physiologic elimination of cells. These include cancer cells, skin cells as described in the question, and others. It mainly involves the release of sequestered enzymes and mediators from within an apoptotic cell, such as from the Golgi apparatus or lysosomes.
Apoptosis is the normal, physiologic elimination of cells. These include cancer cells, skin cells as described in the question, and others. It mainly involves the release of sequestered enzymes and mediators from within an apoptotic cell, such as from the Golgi apparatus or lysosomes.
Compare your answer with the correct one above
The mechanism by which a macrophage engulfs cellular debris and/or pathogens is best described as
.
The mechanism by which a macrophage engulfs cellular debris and/or pathogens is best described as .
Macrophages are immune cells that phagocytize cell debris and pathogens, then fuse with lysosomes to digest the material. Receptor-mediated endocytosis is a form of endocytosis primarily involved in viral infection or protein uptake. Pinocytosis refers to the uptake of liquid, specifically, from the extracellular medium. Exocytosis is the opposite of what is being described in this question.
Macrophages are immune cells that phagocytize cell debris and pathogens, then fuse with lysosomes to digest the material. Receptor-mediated endocytosis is a form of endocytosis primarily involved in viral infection or protein uptake. Pinocytosis refers to the uptake of liquid, specifically, from the extracellular medium. Exocytosis is the opposite of what is being described in this question.
Compare your answer with the correct one above
Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A novel cell line is created that lacks PrPC. These cells are functionally normal except they grow uncontrollably and do not appear to have a finite number of divisions. PrPC is thus most likely involved in which process?
Prions are the suspected cause of a wide variety of neurodegenerative diseases in mammals. According to prevailing theory, prions are infectious particles made only of protein and found in high concentrations in the brains of infected animals. All mammals produce normal prion protein, PrPC, a transmembrane protein whose function remains unclear.
Infectious prions, PrPRes, induce conformational changes in the existing PrPC proteins according to the following reaction:
PrPC + PrPRes → PrPRes + PrPRes
The PrPRes is then suspected to accumulate in the nervous tissue of infected patients and cause disease. This model of transmission generates replicated proteins, but does so bypassing the standard model of the central dogma of molecular biology. Transcription and translation apparently do not play a role in this replication process.
This theory is a major departure from previously established biological dogma. A scientist decides to test the protein-only theory of prion propagation. He establishes his experiment as follows:
Homogenized brain matter of infected rabbits is injected into the brains of healthy rabbits, as per the following table:
Rabbit 1 and 2: injected with normal saline on days 1 and 2
The above trials serve as controls.
Rabbit 3 and 4: injected with homogenized brain matter on days 1 and 2
The above trials use unmodified brain matter.
Rabbit 5 and 6: injected with irradiated homogenized brain matter on days 1 and 2
The above trials use brain matter that has been irradiated to destroy nucleic acids in the homogenate.
Rabbit 7 and 8: injected with protein-free centrifuged homogenized brain matter on days 1 and 2
The above trials use brain matter that has been centrifuged to generate a protein-free homogenate and a protein-rich homogenate based on molecular weight.
Rabbit 9 and 10: injected with boiled homogenized brain matter on days 1 and 2
The above trials use brain matter that have been boiled to destroy any bacterial contaminants in the homogenate.
A novel cell line is created that lacks PrPC. These cells are functionally normal except they grow uncontrollably and do not appear to have a finite number of divisions. PrPC is thus most likely involved in which process?
Apoptosis is programmed cell death. If cells are growing uncontrollably without a natural end to their growth patterns, they are likely not undergoing apoptosis.
Apoptosis is programmed cell death. If cells are growing uncontrollably without a natural end to their growth patterns, they are likely not undergoing apoptosis.
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Most scientists subscribe to the theory of endosymbiosis to explain the presence of mitochondria in eukaryotic cells. According to the theory of endosymbiosis, early pre-eukaryotic cells phagocytosed free living prokaryotes, but failed to digest them. As a result, these prokaryotes remained in residence in the pre-eukaryotes, and continued to generate energy. The host cells were able to use this energy to gain a selective advantage over their competitors, and eventually the energy-producing prokaryotes became mitochondria.
In many ways, mitochondria are different from other cellular organelles, and these differences puzzled scientists for many years. The theory of endosymbiosis concisely explains a number of these observations about mitochondria. Perhaps most of all, the theory explains why aerobic metabolism is entirely limited to this one organelle, while other kinds of metabolism are more distributed in the cellular cytosol.
Cells with abnormalities in critical systems, such as mitochondria, will often undergo apoptosis. Which of the following is true of apoptosis?
Most scientists subscribe to the theory of endosymbiosis to explain the presence of mitochondria in eukaryotic cells. According to the theory of endosymbiosis, early pre-eukaryotic cells phagocytosed free living prokaryotes, but failed to digest them. As a result, these prokaryotes remained in residence in the pre-eukaryotes, and continued to generate energy. The host cells were able to use this energy to gain a selective advantage over their competitors, and eventually the energy-producing prokaryotes became mitochondria.
In many ways, mitochondria are different from other cellular organelles, and these differences puzzled scientists for many years. The theory of endosymbiosis concisely explains a number of these observations about mitochondria. Perhaps most of all, the theory explains why aerobic metabolism is entirely limited to this one organelle, while other kinds of metabolism are more distributed in the cellular cytosol.
Cells with abnormalities in critical systems, such as mitochondria, will often undergo apoptosis. Which of the following is true of apoptosis?
Apoptosis and necrosis are distinct processes. Apoptosis is a biologically healthy death of cells, self-limiting and helpful in the elimination of abnormal cells. Necrosis is a pathological state of cell death, and drives inflammation.
Apoptosis and necrosis are distinct processes. Apoptosis is a biologically healthy death of cells, self-limiting and helpful in the elimination of abnormal cells. Necrosis is a pathological state of cell death, and drives inflammation.
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Which cells would be expected to have the highest rate of endocytosis?
Which cells would be expected to have the highest rate of endocytosis?
Endocytosis is the uptake of extracellular materials in vesicles. After release of neurotransmitter into the synaptic cleft, neurons are able to re-uptake the neurotransmitter via endocytosis. This allows them to recycle the cell membrane and molecular components that are released during an action potential.
Erythrocytes are red blood cells, osteoblasts are bone-producing cells, and B-cells are responsible for producing antibodies. None of these cell types plays a significant role in particulate uptake. One should note, however, that while B-cells do not frequently use endocytosis, cytotoxic T-cells are able to phagocytose cellular debris through endocytosis.
Endocytosis is the uptake of extracellular materials in vesicles. After release of neurotransmitter into the synaptic cleft, neurons are able to re-uptake the neurotransmitter via endocytosis. This allows them to recycle the cell membrane and molecular components that are released during an action potential.
Erythrocytes are red blood cells, osteoblasts are bone-producing cells, and B-cells are responsible for producing antibodies. None of these cell types plays a significant role in particulate uptake. One should note, however, that while B-cells do not frequently use endocytosis, cytotoxic T-cells are able to phagocytose cellular debris through endocytosis.
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