Stromal Gli2 activity coordinates a niche signaling program for mammary epithelial stem cells

Author:

Zhao Chen12ORCID,Cai Shang1ORCID,Shin Kunyoo123,Lim Agnes14ORCID,Kalisky Tomer5,Lu Wan-Jin12ORCID,Clarke Michael F.1,Beachy Philip A.1246ORCID

Affiliation:

1. Institute for Stem Cell Biology and Regenerative Medicine, Stanford University School of Medicine, Stanford, CA 94305, USA.

2. Department of Biochemistry, Stanford University School of Medicine, Stanford, CA 94305, USA.

3. Department of Life Sciences, Pohang University of Science and Technology, Pohang, Gyumgbuk 37673, South Korea.

4. Department of Developmental Biology, Stanford University School of Medicine, Stanford, CA 94305, USA.

5. Faculty of Engineering and Institute for Nanotechnology and Advanced Materials, Bar-Ilan University, Ramat Gan 52900, Israel.

6. Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, CA 94305, USA.

Abstract

Double duty for mammary stem cell niche The stem cell niche is a complex local signaling microenvironment that regulates stem cell activity for tissue and organ maintenance and regeneration. As well as responding locally, during puberty, the mammary gland stem cell niche also responds to systemic hormonal signals. Zhao et al. have found that Gli2, a transcriptional effector of Hedgehog signaling, coordinates the niche-signaling program and activates expression of receptors for the mammatrophic hormones estrogen and growth hormone throughout the mammary gland (see the Perspective by Robertson). Disease may result not only from stem cell defects, but also from dysregulation of the microenvironment. Science , this issue p. eaal3485 ; see also p. 250

Funder

U.S. Department of Defense

Howard Hughes Medical Institute

Breast Cancer Research Foundation

Susan G. Komen

Ludwig Institute for Cancer Research

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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