Published October 12, 2012 | Version v1
Journal article

Co-culture with Sertoli cells promotes proliferation and migration of umbilical cord mesenchymal stem cells

  • 1. Department of Anatomy, Sanquan College, Xinxiang Medical University, Henan 453003, People's Republic of China (China)
  • 2. Department of Histology and Embryology, Guiyang Medical University, Guizhou 550004, People's Republic of China (China)
  • 3. ICU Center, The Third Hospital of Xinxiang Medical University, Henan 453003, People's Republic of China (China)
  • 4. Stem Cell Center, Xinxiang Medical University, Henan 453003, People's Republic of China (China)

Description

Highlights: ► Co-culture of Sertoli cells (SCs) with human umbilical cord mesenchymal stem cells (UCMSCs). ► Presence of SCs dramatically increased proliferation and migration of UCMSCs. ► Presence of SCs stimulated expression of Mdm2, Akt, CDC2, Cyclin D, CXCR4, MAPKs. -- Abstract: Human umbilical cord mesenchymal stem cells (hUCMSCs) have been recently used in transplant therapy. The proliferation and migration of MSCs are the determinants of the efficiency of MSC transplant therapy. Sertoli cells are a kind of "nurse" cells that support the development of sperm cells. Recent studies show that Sertoli cells promote proliferation of endothelial cells and neural stem cells in co-culture. We hypothesized that co-culture of UCMSCs with Sertoli cells may also promote proliferation and migration of UCMSCs. To examine this hypothesis, we isolated UCMSCs from human cords and Sertoli cells from mouse testes, and co-cultured them using a Transwell system. We found that UCMSCs exhibited strong proliferation ability and potential to differentiate to other cell lineages such as osteocytes and adipocytes. The presence of Sertoli cells in co-culture significantly enhanced the proliferation and migration potential of UCMSCs (P < 0.01). Moreover, these phenotypic changes were accompanied with upregulation of multiple genes involved in cell proliferation and migration including phospho-Akt, Mdm2, phospho-CDC2, Cyclin D1, Cyclin D3 as well as CXCR4, phospho-p44 MAPK and phospho-p38 MAPK. These findings indicate that Sertoli cells boost UCMSC proliferation and migration potential.

Availability note (English)

Available from http://dx.doi.org/10.1016/j.bbrc.2012.09.007

Additional details

Identifiers

DOI
10.1016/j.bbrc.2012.09.007;
PII
S0006-291X(12)01734-2;

Publishing Information

Journal Title
Biochemical and Biophysical Research Communications
Journal Volume
427
Journal Issue
1
Journal Page Range
p. 86-90
ISSN
0006-291X
CODEN
BBRCA9

INIS

Country of Publication
United States
Country of Input or Organization
International Atomic Energy Agency (IAEA)
INIS RN
45031202
Subject category
S60: APPLIED LIFE SCIENCES;
Descriptors DEI
BONE CELLS; CELL PROLIFERATION; MICE; PROLIFERATION; SPERMATOZOA; STEM CELLS; TESTES; TRANSPLANTS
Descriptors DEC
ANIMAL CELLS; ANIMALS; BODY; CONNECTIVE TISSUE CELLS; GAMETES; GERM CELLS; GONADS; MALE GENITALS; MAMMALS; ORGANS; RODENTS; SOMATIC CELLS; VERTEBRATES

Optional Information

Copyright
Copyright (c) 2012 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.