Roles of sphingosine-1-phosphate signaling in angiogenesis |
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Authors: | Takuwa Yoh Du Wa Qi Xun Okamoto Yasuo Takuwa Noriko Yoshioka Kazuaki |
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Affiliation: | Yoh Takuwa, Wa Du, Xun Qi, Yasuo Okamoto, Noriko Takuwa, Kazuaki Yoshioka, Department of Physiology, Kanazawa University Graduate School of Medicine, 13-1 Takara-machi, Kanazawa, Ishikawa 920-8640, Japan;Noriko Takuwa, Department of Health and Medical Sciences, Ishikawa Prefectural Nursing University, 7-1 Nakanuma-tu, Kahoku, Ishikawa 929-1212, Japan |
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Abstract: | Sphingosine-1-phosphate (S1P) is a blood-borne lipid mediator with pleiotropic biological activities. S1P acts via the specific cell surface G-protein-coupled receptors, S1P(1-5). S1P(1) and S1P(2) were originally identified from vascular endothelial cells (ECs) and smooth muscle cells, respectively. Emerging evidence shows that S1P plays crucial roles in the regulation of vascular functions, including vascular formation, barrier protection and vascular tone via S1P(1), S1P(2) and S1P(3). In particular, S1P regulates vascular formation through multiple mechanisms; S1P exerts both positive and negative effects on angiogenesis and vascular maturation. The positive and negative effects of S1P are mediated by S1P(1) and S1P(2), respectively. These effects of S1P(1) and S1P(2) are probably mediated by the S1P receptors expressed in multiple cell types including ECs and bone-marrow-derived cells. The receptor-subtype-specific, distinct effects of S1P favor the development of novel therapeutic tactics for antitumor angiogenesis in cancer and therapeutic angiogenesis in ischemic diseases. |
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Keywords: | Sphingosine-1-phosphate Angiogenesis Angiogenic therapy Rac Akt Vascular maturation Endothelial cells Bone-marrow-derived cells |
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