Cell autonomy of HIF effects in Drosophila:: Tracheal cells sense hypoxia and induce terminal branch sprouting

被引:91
作者
Centanin, Lazaro [1 ,2 ]
Dekanty, Andres [1 ,2 ]
Romero, Nuria [1 ,2 ]
Irisarri, Maximiliano [1 ,2 ]
Gorr, Thomas A. [3 ,4 ]
Wappner, Pablo [1 ,2 ]
机构
[1] FCEyN Univ Buenos Aires, CONICET, Inst Leloir, RA-1405 Buenos Aires, DF, Argentina
[2] FCEyN Univ Buenos Aires, CONICET, FBMC, RA-1405 Buenos Aires, DF, Argentina
[3] Univ Zurich, Inst Vet Physiol, Vetsuisse Fac, CH-8057 Zurich, Switzerland
[4] Univ Zurich, Inst Vet Physiol, Zurich Ctr Integrat Human Physiol ZIHP, CH-8057 Zurich, Switzerland
关键词
D O I
10.1016/j.devcel.2008.01.020
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Drosophila tracheal terminal branches are plastic and have the capacity to sprout out projections toward oxygen-starved areas, in a process analogous to mammalian angiogenesis. This response involves the upregulation of FGF/Branchless in hypoxic tissues, which binds its receptor Breathless on tracheal cells. Here, we show that extra sprouting depends on the Hypoxia-Inducible Factor (HIF)-alpha homolog Sima and on the HIF-prolyl hydroxylase Fatiga that operates as an oxygen sensor. In mild hypoxia, Sima accumulates in tracheal cells, where it induces breathless, and this induction is sufficient to provoke tracheal extra sprouting. In nontracheal cells, Sima contributes to branchless induction, whereas overexpression of Sima fails to attract terminal branch outgrowth, suggesting that HIF-independent components are also required for full induction of the ligand. We propose that the autonomous response to hypoxia that occurs in tracheal cells enhances tracheal sensitivity to increasing Branchless levels, and that this mechanism is a cardinal step in hypoxia-dependent tracheal sprouting.
引用
收藏
页码:547 / 558
页数:12
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