ZFIN ID: ZDB-PUB-130313-13
Functional inhibition of UQCRB suppresses angiogenesis in zebrafish
Cho, Y.S., Jung, H.J., Seok, S.H., Payumo, A.Y., Chen, J.K., and Kwon, H.J.
Date: 2013
Source: Biochemical and Biophysical Research Communications   433(4): 396-400 (Journal)
Registered Authors: Chen, James K., Jung, Hye
Keywords: none
MeSH Terms:
  • Amino Acid Sequence
  • Animals
  • Bridged Bicyclo Compounds/pharmacology
  • Carrier Proteins/genetics
  • Carrier Proteins/metabolism*
  • Dose-Response Relationship, Drug
  • Embryo, Nonmammalian/drug effects
  • Embryo, Nonmammalian/physiology
  • Embryonic Development
  • Gene Expression Regulation, Developmental*
  • Gene Knockdown Techniques
  • Mitochondria/genetics
  • Mitochondria/metabolism
  • Molecular Sequence Data
  • Morpholinos/pharmacology
  • Neovascularization, Physiologic/genetics*
  • Prognosis
  • Vascular Endothelial Growth Factor A/genetics
  • Vascular Endothelial Growth Factor A/metabolism
  • Zebrafish/genetics
  • Zebrafish/physiology*
PubMed: 23454382 Full text @ Biochem. Biophys. Res. Commun.
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ABSTRACT

As a subunit of mitochondrial complex III, UQCRB plays an important role in complex III stability, electron transport, and cellular oxygen sensing. Herein, we report UQCRB function regarding angiogenesis in vivo with the zebrafish (Danio rerio). UQCRB knockdown inhibited angiogenesis in zebrafish leading to the suppression of VEGF expression. Moreover, the UQCRB-targeting small molecule terpestacin also inhibited angiogenesis and VEGF levels in zebrafish, supporting the role of UQCRB in angiogenesis. Collectively, UQCRB loss of function by either genetic and pharmacological means inhibited angiogenesis, indicating that UQCRB plays a key role in this process and can be a prognostic marker of angiogenesis- and mitochondria-related diseases.

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