4.7 Article

BMP-2 induces angiogenesis by provoking integrin alpha 6 expression in human endothelial progenitor cells

Journal

BIOCHEMICAL PHARMACOLOGY
Volume 150, Issue -, Pages 254-264

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.bcp.2018.02.021

Keywords

Bone morphogenetic proteins-2; Endothelial progenitor cells; Integrin alpha 6; Angiogenesis

Funding

  1. National Science Council of Taiwan [NSC 99-2632-B-715-001-MY3]
  2. Ministry of Science and Technology of Taiwan [MOST 102-2632-B-715-001-MY3, MOST 105-2632-B-715-001, MOST 106-2320-B-029-002, MOST 106-2320-B-715-001-MY3]
  3. Mackay Medical College [MMC-1061B02]
  4. Mackay Memorial Hospital [MMH-MM-10507]
  5. Taipei City Hospital [TPCH-107-021]

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Bone morphogenetic protein-2 (BMP-2) is a multifunctional cytokine, capable of governing several cellular functions, including proliferation, motility, differentiation, and angiogenesis. Circulating endothelial progenitor cells (EPCs) have been shown to facilitate tissue repair, postnatal neovascularization, and tumor associated angiogenesis. Nevertheless, the impact of BMP-2 on angiogenesis of human EPCs has largely remained a mystery. In this study, we found that BMP-2 promoted cell migration and tube formation of EPCs in a concentration dependent manner, indicating BMP-2 induced in vitro angiogenesis in human EPCs. Furthermore, BMP-2 significantly increased microvessel formation in Matrigel plug assay, and BMP-2 antagonist noggin prevented BMP2-induced in vivo angiogenesis. Mechanistic investigations showed BMP-2 profoundly induced the expression of Id-1 and integrin a6 as well as EPCs angiogenesis by activating PI3K/Akt and MEK/ERK signaling pathways. Moreover, knockdown of Id-1 and integrin a6 by siRNA transfection obviously attenuated BMP-2-indueced tube formation of EPCs. These results suggest that BMP-2 promotes angiogenesis in human EPCs through the activation of PI3K/Akt, MEK/ERK, and Id-1/integrin a6 signaling cascades. This is the first demonstration that BMP2 exhibits the angiogenesis property on human EPCs. BMP-2 might serve as the potential therapeutic target for treatment of angiogenesis-related diseases.

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