D-Ala2-GIP (1-30) 通过通过Epac/Rap1/Cdc42信号通路促进内皮细胞迁移促进血管生成

Tuchen Guan1, Wenxue Zhang1, Mingxuan Li1

  • 1Key Laboratory of Neuroregeneration of Jiangsu Province and Ministry of Education, Co-innovation Center of Neuroregeneration, Nantong University, Nantong, Jiangsu Province 226001, China.

Cellular signalling
|January 24, 2025
PubMed
概括

胃抑制性多 (GIP) 和其受体 (GIPR) 是新发现的血管生成调节剂. 这项研究揭示了GIP通过cAMP-Epac/Rap1/Cdc42通路促进血管形成,为心血管生物学提供了洞察力.

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