Loss of FKBP5 impedes adipocyte differentiation under both normoxia and hypoxic stress

Lingling Zhang, Bin Qiu, Tingting Wang, Jun Wang, Ming Liu, Yuxue Xu, Chao Wang, Ran Deng, Kent Williams, Zhiwei Yang, Tiebing Liang, Weidong Yong

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

FK506-binding protein 51 (FKBP51) is one of the most important regulators in the GR-mediated stress response, and we previously demonstrated that loss of FKBP5 arrests adipogenesis and renders mice resistant to diet-induced obesity (DIO). However, the exact role of FKBP5 in the process of adipocyte differentiation under hypoxic conditions (the common microenvironment where adipocytes reside in obese individuals) is still unclear. Here, by isolating and culturing WT- and Fkbp5-knockout mouse embryonic fibroblasts (MEFs), and treat them at normal oxygen environment (21% O2, nomorxia) or low oxygen environment (5% O2, hypoxia). Enhanced adipogenesis were observed at hypoxia when compared to normal oxygen environment. The loss of FKBP5 significantly prevents the adipogenesis from KO MEFs under nomorxia condition, with subtle enhancement of adipogenesis at hypoxia condition, which is similar as observed in WT-MEFs at hypoxia condition but with obvious enhancement of adipogenesis. Importantly, the protein level of FKBP5 reduced in undifferentiated MEFs under acute hypoxic stress (24 h), but drastically increased during the mid-late stage of adipocyte (Day 6) differentiation from WT-MEFs under chronic hypoxia. Furthermore, we find under normal and hypoxic conditions that FKBP5 deletion alters the expression profile of adipogenesis-related genes, including those involved in lipogenesis, lipolysis, and energy metabolism, which partially explains the compromised adipocyte differentiation in FKBP51-KO MEFs. Taken together, our findings identify a novel role of FKBP5 in hypoxia-regulated adipogenesis, and provide a candidate for anti-obesity strategies targeting FKBP51.

Original languageEnglish (US)
Pages (from-to)761-767
Number of pages7
JournalBiochemical and Biophysical Research Communications
Volume485
Issue number4
DOIs
StatePublished - Apr 15 2017

Fingerprint

Adipogenesis
Fibroblasts
Adipocytes
Tacrolimus Binding Proteins
Oxygen
Obesity
Lipogenesis
Nutrition
Lipolysis
Knockout Mice
Energy Metabolism
Genes
Hypoxia
Diet
Proteins

Keywords

  • Adipogenesis
  • FKBP5
  • Glucocorticoid receptor
  • Hypoxic stress
  • Mouse embryonic fibroblasts

ASJC Scopus subject areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

Loss of FKBP5 impedes adipocyte differentiation under both normoxia and hypoxic stress. / Zhang, Lingling; Qiu, Bin; Wang, Tingting; Wang, Jun; Liu, Ming; Xu, Yuxue; Wang, Chao; Deng, Ran; Williams, Kent; Yang, Zhiwei; Liang, Tiebing; Yong, Weidong.

In: Biochemical and Biophysical Research Communications, Vol. 485, No. 4, 15.04.2017, p. 761-767.

Research output: Contribution to journalArticle

Zhang, L, Qiu, B, Wang, T, Wang, J, Liu, M, Xu, Y, Wang, C, Deng, R, Williams, K, Yang, Z, Liang, T & Yong, W 2017, 'Loss of FKBP5 impedes adipocyte differentiation under both normoxia and hypoxic stress', Biochemical and Biophysical Research Communications, vol. 485, no. 4, pp. 761-767. https://doi.org/10.1016/j.bbrc.2017.02.126
Zhang, Lingling ; Qiu, Bin ; Wang, Tingting ; Wang, Jun ; Liu, Ming ; Xu, Yuxue ; Wang, Chao ; Deng, Ran ; Williams, Kent ; Yang, Zhiwei ; Liang, Tiebing ; Yong, Weidong. / Loss of FKBP5 impedes adipocyte differentiation under both normoxia and hypoxic stress. In: Biochemical and Biophysical Research Communications. 2017 ; Vol. 485, No. 4. pp. 761-767.
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AU - Wang, Chao

AU - Deng, Ran

AU - Williams, Kent

AU - Yang, Zhiwei

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AU - Yong, Weidong

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