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GM-CSF Enhances Mobilization of Bone Marrow Mesenchymal Stem Cells via a CXCR4-Medicated Mechanism
- Kim, Jiyoung;
- Kim, Na Kyeong;
- Park, So Ra;
- Choi, Byung Hyune
WEB OF SCIENCE
22SCOPUS
27초록
Background:This study was conducted to investigate the effect of granulocyte-macrophage colony-stimulating factor (GM-CSF) on the mobilization of mesenchymal stem cells (MSCs) from the bone marrow (BM) into the peripheral blood (PB) in rats.Methods:GM-CSF was administered subcutaneously to rats at 50g/kg body weight for 5 consecutive days. The BM and PB of rats were collected at 1, 3, and 5days during the administration for analysis.Results:Upon GM-CSF administration, the number of mononuclear cells increased rapidly at day 1 both in the BM and PB. This number decreased gradually over time in the BM to below the initial amount by day 5, but was maintained at a high level in the PB until day 5. The colony-forming unit-fibroblasts were increased in the PB by 10.3-fold at day 5 of GM-CSF administration, but decreased in the BM. Compared to GM-CSF, granulocyte-colony stimulating factor (G-CSF) stimulated lower levels of MSC mobilization from the BM to the PB. Immunohistochemical analysis revealed that GM-CSF induced a hypoxic and proteolytic microenvironment and increased C-X-C chemokine receptor type 4 (CXCR4) expression in the BM. GM-CSF added to BM MSCs in vitro dose-dependently increased CXCR4 expression and cell migration. G-CSF and stromal cell derived factor-1 (SDF-1) showed similar results in these in vitro assays. Know-down of CXCR4 expression with siRNA significantly abolished GM-CSF- and G-CSF-induced MSC migration in vitro, indicating the involvement of the SDF-1-CXCR4 interaction in the mechanism.Conclusion:These results suggest that GM-CSF is a useful tool for mobilizing BM MSCs into the PB.
키워드
- 제목
- GM-CSF Enhances Mobilization of Bone Marrow Mesenchymal Stem Cells via a CXCR4-Medicated Mechanism
- 저자
- Kim, Jiyoung; Kim, Na Kyeong; Park, So Ra; Choi, Byung Hyune
- 발행일
- 2019-02
- 유형
- Article
- 저널명
- 조직공학과 재생의학
- 권
- 16
- 호
- 1
- 페이지
- 59 ~ 68