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MiR-9 Controls Chemotactic Activity of Cord Blood CD34⁺ Cells by Repressing CXCR4 Expression.

Tae Won Ha | Hyun Soo Kang | Tae-Hee Kim | Ji Hyun Kwon | Hyun Kyu Kim | Aeli Ryu | Hyeji Jeon | Jaeseok Han | Hal E Broxmeyer | Yongsung Hwang | Yun Kyung Lee | Man Ryul Lee
International journal of stem cells | 2018

Improved approaches for promoting umbilical cord blood (CB) hematopoietic stem cell (HSC) homing are clinically important to enhance engraftment of CB-HSCs. Clinical transplantation of CB-HSCs is used to treat a wide range of disorders. However, an improved understanding of HSC chemotaxis is needed for facilitation of the engraftment process. We found that ectopic overexpression of miR-9 and antisense-miR-9 respectively down- and up-regulated C-X-C chemokine receptor type 4 (CXCR4) expression in CB-CD34+ cells as well as in 293T and TF-1 cell lines. Since CXCR4 is a specific receptor for the stromal cell derived factor-1 (SDF-1) chemotactic factor, we investigated whether sense miR-9 and antisense miR-9 influenced CXCR4-mediated chemotactic mobility of primary CB CD34+ cells and TF-1 cells. Ectopic overexpression of sense miR-9 and antisense miR-9 respectively down- and up-regulated SDF-1-mediated chemotactic cell mobility. To our knowledge, this study is the first to report that miR-9 may play a role in regulating CXCR4 expression and SDF-1-mediated chemotactic activity of CB CD34+ cells.

Pubmed ID: 30343551

Research resources used in this publication

None found

Antibodies used in this publication

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Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL056416
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL112669
  • Agency: NHLBI NIH HHS, United States
    Id: R35 HL139599
  • Agency: NIDDK NIH HHS, United States
    Id: U54 DK106846

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