[A preliminary study on the culture of single hematopoietic stem cell]

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2012 Feb;34(1):19-24.
[Article in Chinese]

Abstract

Objective: To investigate the biological behavior including survival and proliferation of CD34 + CD38--Lin--cells when they are cultured at single cell level.

Methods: Purified umbilical cord blood CD34 + CD38--Lin--cells were separated at single cell level in 96-well plates using flow cytometry for four groups: control group (CD34 + CD38--Lin--cell plus stem cell medium) , Shh group (CD34 + CD38--Lin--cell plus stem cell medium and Shh), BMP-4 group (CD34 + CD38--Lin--cell plus stem cell medium and BMP-4), Jagged-1 group (CD34 + CD38--Lin--cell plus stem cell medium and Jagged-1). Methylcellulose medium was used in the colony-forming experiment which was also in four groups as previously. The number of cells and colony-forming units in each well for the four groups was evaluated at different time points (day 1, 3, 7) with fluorescence microscopy counting method.

Results: Division of single cell was observed to be amplified in all of these groups from day 3. And meanwhile, after 1-week culture, the survival rates for the treated groups were all higher than the control group (Jagged-1 group > BMP-4 group > Shh group > control), while the cell number in each well was also highest in the Jagged-1 group (Jagged-1 group > BMP-4 group > control). The number of wells with a cell number of zero was significantly fewer in all treated groups (especially the Jagged-1 group) than in the control group; meanwhile, the number of wells with a cell number higher than 17 was evidently higher in all the treated groups (especially the BMP-4 group) more than controls. Colony-forming units for erythroid (BFU-E), granulocyte (CFU-G), macrophage (CFU-M), and granulocyte macrophage (CFU-GM) were observed for all of these experimental groups, and there was no significant difference between the four experimental groups.

Conclusions: CD34 + CD38 - Lin - cell can achieve the survival, self-renewal and proliferation when cultured at single cell level, and the adding of Shh, BMP-4, and Jagged-1 can enhance such capabilities. However, CD34 + CD38 - Lin - cell can only maintain cell totipotency in its niche.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP-ribosyl Cyclase 1 / metabolism
  • Antigens, CD34 / metabolism
  • Bone Morphogenetic Protein 4 / chemistry
  • Calcium-Binding Proteins / chemistry
  • Cell Culture Techniques*
  • Cell Proliferation
  • Cell Survival
  • Cells, Cultured
  • Colony-Forming Units Assay
  • Culture Media
  • Fetal Blood / cytology*
  • Hedgehog Proteins / chemistry
  • Hematopoietic Stem Cells / cytology*
  • Humans
  • Intercellular Signaling Peptides and Proteins / chemistry
  • Jagged-1 Protein
  • Membrane Proteins / chemistry
  • Serrate-Jagged Proteins

Substances

  • Antigens, CD34
  • Bone Morphogenetic Protein 4
  • Calcium-Binding Proteins
  • Culture Media
  • Hedgehog Proteins
  • Intercellular Signaling Peptides and Proteins
  • JAG1 protein, human
  • Jagged-1 Protein
  • Membrane Proteins
  • Serrate-Jagged Proteins
  • ADP-ribosyl Cyclase 1