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Receptor-mediated Endocytosis01:20

Receptor-mediated Endocytosis

Receptor-mediated endocytosis is when bulk amounts of specific molecules are imported into a cell after binding to cell surface receptors. The molecules bound to these receptors are taken into the cell through inward folding of the cell surface membrane, which is eventually pinched off into a vesicle within the cell. Structural proteins, such as clathrin, coat the budding vesicle.
Clathrin-Mediated Endocytosis of LDL
One well-characterized example of receptor-mediated endocytosis is the...
Receptor-mediated Endocytosis01:38

Receptor-mediated Endocytosis

Overview
Receptor-Mediated Endocytosis01:20

Receptor-Mediated Endocytosis

Receptor-mediated endocytosis is when bulk amounts of specific molecules are imported into a cell after binding to cell surface receptors. The molecules bound to these receptors are taken into the cell through inward folding of the cell surface membrane, which is eventually pinched off into a vesicle within the cell. Structural proteins, such as clathrin, coat the budding vesicle.
Clathrin-Mediated Endocytosis of LDL
One well-characterized example of receptor-mediated endocytosis is the...
Retrovirus Life Cycles01:10

Retrovirus Life Cycles

Retroviruses have a single-stranded RNA genome that undergoes a special form of replication. Once the retrovirus has entered the host cell, an enzyme called reverse transcriptase synthesizes double-stranded DNA from the retroviral RNA genome. This DNA copy of the genome is then integrated into the host’s genome inside the nucleus via an enzyme called integrase. Consequently, the retroviral genome is transcribed into RNA whenever the host’s genome is transcribed, allowing the retrovirus to...
Recycling Endosomes and Transcytosis00:58

Recycling Endosomes and Transcytosis

The recycling endosome, also known as the endosomal recycling compartment (ERC), is a part of the slow-recycling process of the endocytic pathway. Molecules internalized through receptor-mediated endocytosis are either degraded in the lysosomes or are recycled to the plasma membrane through the fast- or slow-recycling route.
The recycling endosome is not a single organelle but an extensively tubulated network of recycling pathways. It functions in storing molecules or transporting them across...
Retroviruses02:33

Retroviruses

Retroviruses and retrotransposons both insert copies of their genetic elements into the genome of the host cell. Thus, the viral genes are passed on when the host genome is replicated or translated. A typical retroviral DNA sequence contains 3-4 genes that encode the different proteins required for its structural assembly and function as a molecular parasite. This DNA is transcribed into a single mRNA, which is very similar in structure to conventional mRNAs, i.e., it is capped at the 5’...

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Related Experiment Video

Updated: May 18, 2026

Production of Pseudotyped Particles to Study Highly Pathogenic Coronaviruses in a Biosafety Level 2 Setting
08:40

Production of Pseudotyped Particles to Study Highly Pathogenic Coronaviruses in a Biosafety Level 2 Setting

Published on: March 1, 2019

Reovirus uses multiple endocytic pathways for cell entry.

Wade L Schulz1, Amelia K Haj, Leslie A Schiff

  • 1Department of Microbiology, University of Minnesota, Minneapolis, Minnesota, USA.

Journal of Virology
|September 14, 2012
PubMed
Summary

Reovirus virions use multiple endocytic pathways for cell entry. Uncoated reovirus particles (ISVPs) utilize caveolar endocytosis, independent of clathrin and cholesterol, for infection.

Area of Science:

  • Virology
  • Cell Biology
  • Infectious Disease

Background:

  • Reovirus virion entry typically involves clathrin-mediated endocytosis after binding to junctional adhesion molecule A (JAM-A).
  • Extracellular capsid proteolysis (uncoating) occurs during in vivo reovirus infection, generating intermediate subviral particles (ISVPs).

Purpose of the Study:

  • To investigate the cellular entry mechanisms of reovirus ISVPs.
  • To determine if ISVPs use direct penetration or endocytic pathways for cell entry.
  • To compare ISVP entry pathways with those of intact reovirus virions.

Main Methods:

  • Utilized dynasore (dynamin inhibitor) and genistein/dominant-negative caveolin-1 (caveolar endocytosis inhibitors).
  • Assessed infection inhibition by cholesterol depletion using methyl-β-cyclodextrin.

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Last Updated: May 18, 2026

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  • Investigated pathways independent of clathrin and caveolin.
  • Main Results:

    • Reovirus ISVP entry and infection were inhibited by dynamin and caveolar endocytosis inhibitors.
    • Caveolar endocytosis inhibition also reduced virion infection.
    • Cholesterol depletion inhibited virion infection but not ISVP infection.
    • ISVP entry was independent of clathrin and caveolin.

    Conclusions:

    • Reovirus virions employ both dynamin-dependent and -independent endocytic routes.
    • Reovirus ISVPs preferentially utilize caveolar endocytosis for cellular entry.
    • ISVP entry mechanisms differ from intact virions, particularly regarding cholesterol dependence.