Literature DB >> 33222125

Measuring Endocytosis During Proliferative Cell Quiescence.

Claudia Hinze1,2, Kieran McGourty1,3, Emmanuel Boucrot4,5.   

Abstract

Quiescence (also called "G0") is the state in which cells have exited the cell cycle but are capable to reenter as required. Though poorly understood, it represents one of the most prevalent cell states across all life. Many biologically important cell types reside in quiescence including mature hepatocytes, endothelial cells, and dormant adult stem cells. Furthermore, the quiescence program occurs in both short- and long-term varieties, depending on the physiological environments. A barrier slowing our understanding of quiescence has been a scarcity of available in vitro model systems to allow for the exploration of key regulatory pathways, such as endocytosis. Endocytosis, the internalization of extracellular material into the cell, is a fundamental and highly regulated process that impacts many cell biological functions. Accordingly, we have developed an in vitro model of deep quiescence in hTERT-immortalized RPE1 cells, combining both long-term contact inhibition and mitogen removal, to measure endocytosis. In addition, we present an analytical approach employing automated high-throughput microscopy and image analysis that yields high-content data allowing for meaningful and statistically robust interpretation. Importantly, the methods presented herein provide a suitable platform that can be easily adapted to investigate other regulatory processes across the cell cycle.

Entities:  

Keywords:  Automated high-throughput microscopy; Cell cycle; Cell quiescence; Clathrin-mediated endocytosis; Endocytosis; Epidermal growth factor; Fluid-phase uptake; G0; High-throughput image analysis; Macropinocytosis; Primary cells; hTERT-immortalized cells

Mesh:

Substances:

Year:  2021        PMID: 33222125     DOI: 10.1007/978-1-0716-1044-2_2

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  57 in total

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2.  Cellular quiescence induced by contact inhibition or serum withdrawal in C3H10T1/2 cells.

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Authors:  Bertrand Daignan-Fornier; Isabelle Sagot
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Review 4.  Stationary phase in yeast.

Authors:  Paul K Herman
Journal:  Curr Opin Microbiol       Date:  2002-12       Impact factor: 7.934

Review 5.  "Sleeping beauty": quiescence in Saccharomyces cerevisiae.

Authors:  Joseph V Gray; Gregory A Petsko; Gerald C Johnston; Dagmar Ringe; Richard A Singer; Margaret Werner-Washburne
Journal:  Microbiol Mol Biol Rev       Date:  2004-06       Impact factor: 11.056

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Authors:  Mayda Valentin; Elizabeth Yang
Journal:  Cell Cycle       Date:  2008-09-12       Impact factor: 4.534

7.  Quiescent fibroblasts exhibit high metabolic activity.

Authors:  Johanna M S Lemons; Xiao-Jiang Feng; Bryson D Bennett; Aster Legesse-Miller; Elizabeth L Johnson; Irene Raitman; Elizabeth A Pollina; Herschel A Rabitz; Joshua D Rabinowitz; Hilary A Coller
Journal:  PLoS Biol       Date:  2010-10-19       Impact factor: 8.029

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Authors:  Hilary A Coller; Liyun Sang; James M Roberts
Journal:  PLoS Biol       Date:  2006-03-07       Impact factor: 8.029

9.  Normal and perturbed Chinese hamster ovary cells: correlation of DNA, RNA, and protein content by flow cytometry.

Authors:  H A Crissman; Z Darzynkiewicz; R A Tobey; J A Steinkamp
Journal:  J Cell Biol       Date:  1985-07       Impact factor: 10.539

10.  A map of protein dynamics during cell-cycle progression and cell-cycle exit.

Authors:  Sara Gookin; Mingwei Min; Harsha Phadke; Mingyu Chung; Justin Moser; Iain Miller; Dylan Carter; Sabrina L Spencer
Journal:  PLoS Biol       Date:  2017-09-11       Impact factor: 8.029

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  1 in total

1.  Synthesis of Poly(acrylic acid)-Cysteine-Based Hydrogels with Highly Customizable Mechanical Properties for Advanced Cell Culture Applications.

Authors:  Sharon O Bolanta; Sigita Malijauskaite; Kieran McGourty; Emmet J O'Reilly
Journal:  ACS Omega       Date:  2022-03-11
  1 in total

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