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Related Concept Videos

Interphase00:54

Interphase

The cell cycle occurs over approximately 24 hours (in a typical human cell) and in two distinct stages: interphase, which includes three phases of the cell cycle (G1, S, and G2), and mitosis (M). During interphase, which takes up about 95 percent of the duration of the eukaryotic cell cycle, cells grow and replicate their DNA in preparation for mitosis.
COP Coated Vesicles00:59

COP Coated Vesicles

Membrane-enclosed structures called vesicles transport proteins and lipids across the cell. The vesicles derive their cargo from the plasma membrane, Golgi, ER, or endosome. Coated vesicles are spherical, protein-coated carriers with a 50–100 nm diameter that mediate bidirectional transport between the ER and the Golgi. The distribution of proteins between the ER and Golgi complex is dynamic and is maintained by different coated vesicles. Their formation is driven by the assembly of different...
Pinching-off of Coated Vesicles01:32

Pinching-off of Coated Vesicles

Vesicle budding is orchestrated by distinct cytosolic proteins such as adaptor proteins, coat proteins, and GTPases. To initiate vesicle budding, membrane-bending proteins containing crescent-shaped BAR domains bind to the lipid heads in the bilayer and distort the membrane to form a protein-coated vesicle bud. Adaptors proteins such as AP2 for clathrin-coated vesicles can nucleate on the deformed membrane. Finally, coat proteins such as clathrin or COPI and COPII assemble into a coat forming...
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As cells progress into mitosis, the nuclear envelope breaks down, and the condensed chromosomes are exposed to the array of bipolar microtubules of the mitotic spindle. The kinetochore, a large, disc-shaped protein complex, is present at the centromere region of the sister chromatids and acts as a binding site for the microtubules.  Usually, the plus-end of a single microtubule is embedded within the kinetochore. However, some kinetochores first establish lateral contact with the side-wall of a...
Interphase00:56

Interphase

The cell cycle occurs over approximately 24 hours (in a typical human cell) and in two distinct stages: interphase, which includes three phases of the cell cycle (G1, S, and G2), and mitosis (M). During interphase, which takes up about 95 percent of the duration of the eukaryotic cell cycle, cells grow and replicate their DNA in preparation for mitosis.
Phases of Interphase
Following each period of mitosis and cytokinesis, eukaryotic cells enter interphase, during which they grow and replicate...

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Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis
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Combining Mitotic Cell Synchronization and High Resolution Confocal Microscopy to Study the Role of Multifunctional Cell Cycle Proteins During Mitosis

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Coated pits in interphase and mitotic A431 cells.

M Pypaert1, J M Lucocq, G Warren

  • 1Department of Biochemistry, University, Dundee, Scotland.

European Journal of Cell Biology
|December 1, 1987
PubMed
Summary

This study examined how endocytosis is affected during mitosis in A431 cells. Endocytosis is a process where cells take in materials through structures called coated pits. The researchers found that during mitosis, the process is inhibited, but the exact point of inhibition was unclear. They compared the stages of budding in interphase and mitotic cells and found that all stages of budding were present in mitotic cells. However, flatter coated pits were more common in mitotic cells, possibly due to their larger size. The study concluded that if endocytosis is inhibited during mitosis, it must affect all stages of the budding process equally.

Keywords:
endocytosis inhibitionmitotic cell cyclecoated pit morphologycellular analysis

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Area of Science:

  • Cell biology
  • Cytoskeletal dynamics
  • Endocytosis mechanisms

Background:

Endocytosis involves the internalization of materials via coated pits. Prior research has shown that this process is disrupted during mitosis in certain cell types. However, the exact mechanism causing this disruption remains unclear. No prior work had resolved whether inhibition occurs at a specific stage of budding or affects all stages equally. This uncertainty drove the need for a detailed comparison between interphase and mitotic cells. Researchers sought to determine if the inhibition is localized or widespread. They focused on the morphological changes in coated pits across cell cycle stages. The study aimed to clarify the relationship between cell cycle progression and endocytotic activity. Understanding this could provide insights into how cellular processes are regulated during division.

Purpose Of The Study:

The purpose of the study was to investigate the inhibition of endocytosis during mitosis in A431 cells. The researchers aimed to determine whether the inhibition occurs at a specific stage of the budding process or affects all stages. They compared the distribution of budding stages between interphase and mitotic cells. The motivation was to clarify the mechanism behind the observed endocytosis inhibition. By quantifying the extent of budding, they sought to identify any differences in pit morphology. The study focused on the frequency and shape of coated pits in mitotic cells. The goal was to assess whether flattening of pits correlates with inhibition. This could help distinguish between localized and global disruptions in endocytosis.

Main Methods:

The study employed a quantitative approach to measure budding in coated pits. Researchers analyzed cells at various stages of the cell cycle. They compared interphase and mitotic cells using morphological criteria. The extent of budding was assessed by examining pit shapes and frequencies. The method involved identifying and categorizing different stages of budding. The researchers documented the presence of all budding stages in mitotic cells. They noted the increased frequency of flatter pits in mitotic cells. The method also considered the size differences between interphase and mitotic cells.

Main Results:

The study found that all stages of budding observed in interphase cells were also present in mitotic cells. Flatter coated pits were more common in mitotic cells compared to interphase cells. This increased frequency may be partly or entirely due to the larger size of mitotic cells. The presence of all budding stages suggests inhibition is not limited to a single phase. The findings indicate that any inhibition must affect the entire budding process. The researchers observed no exclusive budding stages in mitotic cells. The data suggest that the inhibition is not localized to a specific morphological change. The results highlight the need to consider cell size when interpreting pit morphology.

Conclusions:

The researchers concluded that inhibition of endocytosis during mitosis must occur at all stages of the budding process. They found no evidence of exclusive budding stages in mitotic cells. The increased frequency of flatter pits correlates with cell size differences. The study suggests that inhibition is not localized to a specific morphological change. The findings support the idea that the inhibition is global rather than stage-specific. The researchers emphasize the importance of considering cell size in future studies. Their results align with the hypothesis that inhibition affects all budding phases equally. This conclusion is based solely on the observed morphological and quantitative data.

The main finding is that inhibition of endocytosis during mitosis affects all stages of the budding process, not just one specific stage.

The researchers used a quantitative method to measure and compare the morphological stages of budding in interphase and mitotic cells.

The increased frequency of flatter pits in mitotic cells may be partly or entirely due to their larger size, according to the study.

The presence of all budding stages in mitotic cells suggests that endocytosis inhibition is not limited to a specific phase of the process.

The study found no exclusive budding stages in mitotic cells, indicating that inhibition is global rather than localized to a specific morphological change.

The findings suggest that future research should consider cell size when interpreting coated pit morphology in mitotic cells.