Membrane-bound SCF and VCAM-1 synergistically regulate the morphology of hematopoietic stem cells

Author:

Hao Jia1ORCID,Zhou Hao1,Nemes Kristen1,Yen Daniel1,Zhao Winfield1,Bramlett Charles2,Wang Bowen2ORCID,Lu Rong1234,Shen Keyue135ORCID

Affiliation:

1. Department of Biomedical Engineering, University of Southern California, Los Angeles, CA

2. Department of Stem Cell Biology and Regenerative Medicine, University of Southern California, Los Angeles, CA

3. Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA

4. Department of Medicine, University of Southern California, Los Angeles, CA

5. USC Stem Cell, University of Southern California, Los Angeles, CA

Abstract

Membrane-bound factors expressed by niche stromal cells constitute a unique class of localized cues and regulate the long-term functions of adult stem cells, yet little is known about the underlying mechanisms. Here, we used a supported lipid bilayer (SLB) to recapitulate the membrane-bound interactions between hematopoietic stem cells (HSCs) and niche stromal cells. HSCs cluster membrane-bound stem cell factor (mSCF) at the HSC-SLB interface. They further form a polarized morphology with aggregated mSCF under a large protrusion through a synergy with VCAM-1 on the bilayer, which drastically enhances HSC adhesion. These features are unique to mSCF and HSCs among the factors and hematopoietic populations we examined. The mSCF–VCAM-1 synergy and the polarized HSC morphology require PI3K signaling and cytoskeletal reorganization. The synergy also enhances nuclear retention of FOXO3a, a crucial factor for HSC maintenance, and minimizes its loss induced by soluble SCF. Our work thus reveals a unique role and signaling mechanism of membrane-bound factors in regulating stem cell morphology and function.

Funder

National Institutes of Health

University of Southern California

Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research

Rose Hills Foundation

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Phi Beta Psi Charity Trust

Publisher

Rockefeller University Press

Subject

Cell Biology

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