J Korean Med Sci.  2001 Feb;16(1):20-24. 10.3346/jkms.2001.16.1.20.

Cell cycling status of human cord blood CD34+ cells during ex vivo expansion is related to the level of very late antigen expression

Affiliations
  • 1Department of Microbiology, Medical Research Center, College of Medicine, Ewha Womans University, Seoul, Korea.

Abstract

Very late antigen-4 (VLA-4), which binds to the extracellular matrix protein fibronectin, is an integrin molecule known to be modulated during mobilization of CD34+ cells, and to be involved in signaling the mobilization stimuli. On the hypothesis that cell cycling status might be different depending on the level of VLA-4 expression, we investigated the DNA contents of human cord blood CD34+ cells during ex vivo expansion by recombinant human thrombopoietin and flt3-ligand with simultaneous measurement of surface VLA-4 at the 1st and 4th week. During this ex vivo expansion, expression of VLA-4 increased and almost all cells became VLA-4+ until the 4th day of culture. Expression of VLA-4 was maintained in the major population of the cultured cells until the 4th week. The cells in S/G2/M phase were greater in number in VLA-4 high fraction than in VLA-4 low fraction (n=4, p<.001). Furthermore, the fraction of cells in S/G2/M phase increased as the expression of VLA-4 became higher. These results suggest that cord blood CD34+ cells expressing high levels of VLA-4 have more proliferative activities.

Keyword

VLA-4; Receptors, Very Late Antigen; Cell Cycle; Fetal Blood; Antigens, CD34; Ex Vivo Expansion

MeSH Terms

Antigens, CD34/analysis*
Cells, Cultured
DNA/analysis
Fetal Blood/cytology*
G2 Phase
Hematopoietic Stem Cells/physiology*
Human
Immunophenotyping
Infant, Newborn
Integrins/analysis*
Receptors, Lymphocyte Homing/analysis*
S Phase

Cited by  1 articles

Stem Cells Expressing Homing Receptors Could be Expanded From Cryopreserved and Unselected Cord Blood
Young-Ho Lee, Jin-Yeong Han, Su-Yeong Seo, Kyeong-Hee Kim, Young-Ah Lee, Young-Seok Lee, Hyung-Sik Lee, Won-Joo Hur, Hun Han, Hyuk-Chan Kwon, Jae-Seok Kim, Hyo-Jin Kim
J Korean Med Sci. 2004;19(5):635-639.    doi: 10.3346/jkms.2004.19.5.635.

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