Published January 24, 2014 | Version v1
Journal article

Ameliorating replicative senescence of human bone marrow stromal cells by PSMB5 overexpression

  • 1. Department of Anatomy, Shanxi Medical University, Taiyuan 030001 (China)
  • 2. Department of Orthopaedics, The Second Affiliated Hospital of Shanxi Medical University, Taiyuan 030001 (China)
  • 3. Department of Anatomy, University of Hong Kong Faculty of Medicine, Hong Kong (Hong Kong)
  • 4. Department of Medicine, University of Hong Kong Faculty of Medicine, Hong Kong (Hong Kong)
  • 5. Laboratory of Metabolic Medicine, Singapore Bioimaging Consortium (SBIC), Agency for Science, Technology and Research - A*STAR (Singapore)
  • 6. School of Biotechnology and Food Engineering, Hefei University of Technology, Hefei 230009 (China)

Description

Highlights: • PSMB5 overexpression restores the differentiation potential of aged hBMSCs. • PSMB5 overexpression enhances the proteasomal activity of late-stage hBMSCs. • PSMB5 overexpression inhibits replicative senescence and improved cell viability. • PSMB5 overexpression promotes cell growth by upregulating the Cyclin D1/CDK4 complex. - Abstract: Multipotent human bone marrow stromal cells (hBMSCs) potentially serve as a source for cell-based therapy in regenerative medicine. However, in vitro expansion was inescapably accompanied with cell senescence, characterized by inhibited proliferation and compromised pluripotency. We have previously demonstrated that this aging process is closely associated with reduced 20S proteasomal activity, with down-regulation of rate-limiting catalytic β-subunits particularly evident. In the present study, we confirmed that proteasomal activity directly contributes to senescence of hBMSCs, which could be reversed by overexpression of the β5-subunit (PSMB5). Knocking down PSMB5 led to decreased proteasomal activity concurrent with reduced cell proliferation in early-stage hBMSCs, which is similar to the senescent phenotype observed in late-stage cells. In contrast, overexpressing PSMB5 in late-stage cells efficiently restored the normal activity of 20S proteasomes and promoted cell growth, possibly via upregulating the Cyclin D1/CDK4 complex. Additionally, PSMB5 could enhance cell resistance to oxidative stress, as evidenced by the increased cell survival upon exposing senescent hBMSCs to hydrogen peroxide. Furthermore, PSMB5 overexpression retained the pluripotency of late-stage hBMSCs by facilitating their neural differentiation both in vitro and in vivo. Collectively, our work reveals a critical role of PSMB5 in 20S proteasome-mediated protection against replicative senescence, pointing to a possible strategy for maintaining the integrity of culture-expanded hBMSCs by manipulating the expression of PSMB5

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2013.12.113

Additional details

Identifiers

DOI
10.1016/j.bbrc.2013.12.113;
PII
S0006-291X(13)02184-0;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
443
Journal Issue
4
Journal Page Range
p. 1182-1188
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
46122134
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
AGING; BONE MARROW; CELL PROLIFERATION; COMPLEXES; DRUGS; HYDROGEN PEROXIDE; IN VITRO; IN VIVO; OXIDATION; PHENOTYPE; REGULATIONS; THERAPY; VIABILITY
Descriptors DEC
ANIMAL TISSUES; BODY; CHEMICAL REACTIONS; HEMATOPOIETIC SYSTEM; HYDROGEN COMPOUNDS; LAWS; MEDICINE; ORGANS; OXYGEN COMPOUNDS; PEROXIDES

Optional Information

Copyright
Copyright (c) 2013 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.