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Zhang, F.* ; Li, Y.* ; Tang, Z.* ; Kumar, A.* ; Lee, C.* ; Zhang, L.* ; Zhu, C.* ; Klotzsche-von Ameln, A.* ; Wang, B.* ; Gao, Z.* ; Zhang, S.* ; Langer, H.F.* ; Hou, X.* ; Jensen, L.* ; Ma, W.* ; Wong, W.* ; Chavakis, T.* ; Liu, Y.* ; Cao, Y.* ; Li, X.*

Proliferative and survival effects of PUMA promote angiogenesis.

Cell Rep. 2, 1272-1285 (2012)
DOI PMC
Open Access Gold as soon as Publ. Version/Full Text is submitted to ZB.
The p53 upregulated modulator of apoptosis (PUMA) is known as an essential apoptosis inducer. Here, we report the seemingly paradoxical finding that PUMA is a proangiogenic factor critically required for the proliferation and survival of vascular and microglia cells. Strikingly, Puma deficiency by genetic deletion or small hairpin RNA knockdown inhibited developmental and pathological angiogenesis and reduced microglia numbers in vivo, whereas Puma gene delivery increased angiogenesis and cell survival. Mechanistically, we revealed that PUMA plays a critical role in regulating autophagy by modulating Erk activation and intracellular calcium level. Our findings revealed an unexpected function of PUMA in promoting angiogenesis and warrant more careful investigations into the therapeutic potential of PUMA in treating cancer and degenerative diseases.
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Publication type Article: Journal article
Document type Scientific Article
Language english
Publication Year 2012
HGF-reported in Year 0
ISSN (print) / ISBN 2211-1247
e-ISSN 2211-1247
Journal Cell Reports
Quellenangaben Volume: 2, Issue: 5, Pages: 1272-1285 Article Number: , Supplement: ,
Publisher Cell Press
Reviewing status Peer reviewed
Institute(s) Institute of Pancreatic Islet Research (IPI)
PubMed ID 23122957
Erfassungsdatum 2012-12-31