Advancing insights into stem cell niche complexities with next-generation technologies.

Curr Opin Cell Biol

Black Family Stem Cell Institute, Icahn School of Medicine at Mount Sinai, Atran Building AB7-10C, Box 1020, 1428 Madison Ave, New York, NY 10029, USA; Department of Cell, Developmental and Regenerative Biology, Icahn School of Medicine at Mount Sinai, Atran Building AB7-10C, Box 1020, 1428 Madison Ave, New York, NY 10029, USA; Department of Dermatology, Icahn School of Medicine at Mount Sinai, Box 1047, One Gustave L. Levy Place, New York, NY 10029, USA,; Graduate School of Biomedical Sciences, Icahn School of Medicine at Mount Sinai, Box 1022, One Gustave L. Levy Place, New York, NY 10029, USA. Electronic address:

Published: December 2018

Adult tissue-specific stem cells are essential for homeostatic tissue maintenance and key to regeneration during injury repair or disease. Many critical stem cell functions rely on the presence of well-timed cues from the microenvironment or niche, which includes a diverse range of components, including neuronal, circulating and extracellular matrix inputs as well as an array of neighboring niche cells directly interacting with the stem cells. However, studies of stem cells and their niche have been challenging due to the complexity of adult stem cell functions, their intrinsic controls and the multiple regulatory niche components. Here, we review recent major advances in our understanding of the complex interplay between stem cells and their niche that were enabled by the tremendous technological leaps in single-cell transcriptome analyses, 3D in vitro cultures and 4D in vivo microscopy of stem cell niches.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6269204PMC
http://dx.doi.org/10.1016/j.ceb.2018.06.012DOI Listing

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