Lysyl oxidase interactions with transforming growth factor-β during angiogenesis are mediated by endothelin 1

被引:10
|
作者
Grunwald, Hagar [1 ,2 ]
Hunker, Kristina L. [3 ]
Birt, Isabelle [3 ]
Aviram, Rohtem [1 ,2 ]
Zaffryar-Eilot, Shelly [1 ,2 ]
Ganesh, Santhi K. [3 ,4 ]
Hasson, Peleg [1 ,2 ]
机构
[1] Technion Israel Inst Technol, Dept Genet & Dev Biol, Rappaport Fac Med, IL-31096 Haifa, Israel
[2] Technion Israel Inst Technol, Res Inst, IL-31096 Haifa, Israel
[3] Univ Michigan, Sch Med, Dept Internal Med, Div Cardiovasc Med, Ann Arbor, MI USA
[4] Univ Michigan, Sch Med, Dept Human Genet, Ann Arbor, MI USA
基金
以色列科学基金会;
关键词
angiogenesis; endothelin; lysyl oxidase; TGF-beta; vascular maturation; MOLECULAR REGULATION; COLLAGEN; STRETCH;
D O I
10.1096/fj.202001860RR
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Crosstalk between multiple components underlies the formation of mature vessels. Although the players involved in angiogenesis have been identified, mechanisms underlying the crosstalk between them are still unclear. Using the ex vivo aortic ring assay, we set out to dissect the interactions between two key angiogenic signaling pathways, vascular endothelial growth factor (VEGF) and transforming growth factor beta (TGF beta), with members of the lysyl oxidase (LOX) family of matrix modifying enzymes. We find an interplay between VEGF, TGF beta, and the LOXs is essential for the formation of mature vascular smooth muscle cells (vSMC)-coated vessels. RNA sequencing analysis further identified an interaction with the endothelin-1 pathway. Our work implicates endothelin-1 downstream of TGF beta in vascular maturation and demonstrate the complexity of processes involved in generating vSMC-coated vessels.
引用
收藏
页数:11
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