Companion Blood Cells Control Ovarian Stem Cell Niche Microenvironment and Homeostasis.

Cell Rep

University of Nice Sophia Antipolis, Institut de Biologie Valrose, iBV, 06108 Nice, France; CNRS, Institut de Biologie Valrose, iBV, UMR 7277, 06108 Nice, France; INSERM, Institut de Biologie Valrose, iBV, U1091, 06108 Nice, France. Electronic address:

Published: October 2015

AI Article Synopsis

  • The extracellular matrix is crucial for how stem cells differentiate and maintain their environment, but its formation and assembly process is not well understood.
  • Researchers discovered that blood cells, specifically a type called plasmatocytes, help create the basement membrane of the Drosophila ovarian germline stem cell niche.
  • Blocking or removing these plasmatocytes during larval development leads to defective adult niches with too many stem cells, highlighting the importance of blood cell interactions in forming and maintaining the stem cell environment.

Article Abstract

The extracellular matrix plays an essential role for stem cell differentiation and niche homeostasis. Yet, the origin and mechanism of assembly of the stem cell niche microenvironment remain poorly characterized. Here, we uncover an association between the niche and blood cells, leading to the formation of the Drosophila ovarian germline stem cell niche basement membrane. We identify a distinct pool of plasmatocytes tightly associated with the developing ovaries from larval stages onward. Expressing tagged collagen IV tissue specifically, we show that the germline stem cell niche basement membrane is produced by these "companion plasmatocytes" in the larval gonad and persists throughout adulthood, including the reproductive period. Eliminating companion plasmatocytes or specifically blocking their collagen IV expression during larval stages results in abnormal adult niches with excess stem cells, a phenotype due to aberrant BMP signaling. Thus, local interactions between the niche and blood cells during gonad development are essential for adult germline stem cell niche microenvironment assembly and homeostasis.

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Source
http://dx.doi.org/10.1016/j.celrep.2015.09.008DOI Listing

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