Published December 2019 | Version v1
Journal article

BMP2-mediated PTEN enhancement promotes differentiation of hair follicle stem cells by inducing autophagy

  • 1. Department of Dermatology, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, 450052, PR (China)
  • 2. College of Basic Medical Sciences, Zhengzhou University, Zhengzhou, 450001, PR (China)
  • 3. Henan Province Medical Instrument Testing Institute, Zhengzhou, 450018, PR (China)

Description

Highlights: • BMP2 promoted the differentiation of HFSCs. • BMP2 facilitated PTEN expression and induced the autophagy of HFSCs. • PTEN induced autophagy and subsequently promoted differentiation of HFSCs. • Autophagy accelerated the differentiation of HFSCs. • BMP2/PTEN axis expedited wound contraction and epidermal regeneration of mice. -- Abstract: The proliferation and differentiation of hair follicle stem cells (HFSCs) is regulated by several signaling pathways, including BMP and PTEN. Therefore, this study intended to clarify the potential effects of two such regulators, BMP2 and PTEN, on HFSC differentiation. HFSCs were subjected to BMP2, noggin (BMP2 ligand inhibitor), rapamycin (Rapa, autophagy inducer), 3-methyladenine (3-MA, autophagy inhibitor), or shRNA against PTEN. The differentiation of HFSCs was evaluated using oil red O staining and autophagy was assessed using the transmission electron microscope. Then expression of epidermal differentiation marker (K10 and involucrin), adipogenic markers (PPAR-γ2, aP2, perilipin2, and Adipoq), keratinocyte-specific marker (K15), proliferation-related markers (PCNA and Ki67) and autophagy-related factors (Atg5, Atg7, Atg12, Beclin-1 and LC3-II/LC3-I) was examined by RT-qPCR and Western blot analysis. Next, HFSCs were treated with 3-MA, or shRNA against Atg5 or Atg7 to verify the effect of autophagy on differentiation of BMP2-treated HFSCs. Finally, the effect of BMP2 on HFSC differentiation was verified by a mouse wound model. HFSCs overexpressing BMP2 exhibited elevated expression of epidermal differentiation marker, adipogenic markers and autophagy-related factors but inhibited expression of keratinocyte-specific marker and proliferation-related markers. Furthermore, we found that PTEN promoted the differentiation of BMP2-treated HFSCs by inducing autophagy. In vivo experiments further confirmed the roles of BMP2/PTEN on differentiation of HFSCs. Taken together, BMP2 up-regulated PTEN and consequently induced autophagy to facilitate HFSC differentiation.

Additional details

Identifiers

DOI
10.1016/j.yexcr.2019.111647;
PII
S0014482719305142;

Publishing Information

Journal Title
Experimental Cell Research
Journal Volume
385
Journal Issue
2
Journal Page Range
vp.
ISSN
0014-4827
CODEN
ECREAL

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
55044450
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
HAIR FOLLICLES; IN VIVO; LIGANDS; MICE; REGENERATION; STEM CELLS; TRANSMISSION ELECTRON MICROSCOPY; WOUNDS
Descriptors DEC
ANIMAL CELLS; ANIMALS; BODY; DISEASES; ELECTRON MICROSCOPY; INJURIES; MAMMALS; MICROSCOPY; ORGANS; RODENTS; SKIN; SOMATIC CELLS; VERTEBRATES

Optional Information

Copyright
Copyright (c) 2019 Published by Elsevier Inc.