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Visualizing the metazoan proliferation-quiescence decision in vivo

Authors :
Robert D Morabito
Nicholas J. Palmisano
Qinyun Zhao
Mingwei Min
Nicholas Weeks
Wan Zhang
Rebecca C. Adikes
Benjamin L. Martin
Jessica L. Feldman
Taylor N. Medwig-Kinney
Nuri Kim
Jayson J. Smith
Sabrina L. Spencer
Abraham Q. Kohrman
Ariel M. Pani
Michael A. Q. Martinez
Michalis Barkoulas
Simeiyun Liu
Ononnah B. Ahmed
Maria D. Sallee
David Q. Matus
Source :
eLife, eLife, Vol 9 (2020)
Publication Year :
2020
Publisher :
eLife Sciences Publications, Ltd, 2020.

Abstract

All living things are made up of cells that form the different tissues, organs and structures of an organism. The human body, for example, is thought to consist of some 37 trillion cells and harbor over 200 cell types. To maintain a working organism, cells divide to create new cells and replace the ones that have died. Cell division is a tightly controlled process consisting of several steps, and cells continuously face a Shakespearean dilemma of deciding whether to continue dividing (also known as cell proliferation) or to halt the process (known as quiescence). This difficult balancing act is critical during all stages of life, from embryonic development to tissue growth in an adult. Problems in the underlying pathways can result in diseases such as cancer. Cell division is driven by proteins called CDKs, which help cells to complete their cell cycle in the correct sequence. To gain more insight into this complex process, scientists have developed tools for monitoring CDKs. One such tool is a fluorescent biosensor, a molecule that can be inserted into cells that glows and moves in response to CDK activity. The biosensor can be studied and measured in each cell using a microscope. Adikes, Kohrman, Martinez et al. adapted and optimized an existing CDK biosensor to help study cell division and the switch between proliferation and quiescence in two common research organisms, the nematode Caenorhabditis elegans and the zebrafish. Analysis of this biosensor showed that CDK activity at the end of cell division is higher if the cells will divide again but is low if the cells are going to become quiescent. This could suggest that the decision of a cell between proliferation and quiescence may happen earlier than expected. The optimized biosensor is sensitive enough to detect these differences and can even measure variations that influence proliferation in a region on C. elegans that was once thought to be unchanging. The development of this biosensor provides a useful research tool that could be used in other living organisms. Many research questions relate to cell division and so the applications of this tool are wide ranging.

Details

ISSN :
2050084X
Volume :
9
Database :
OpenAIRE
Journal :
eLife
Accession number :
edsair.doi.dedup.....9640e3e0789df460d0a9326fc7cafefb
Full Text :
https://doi.org/10.7554/elife.63265