PUBLICATION

Haploinsufficiency of Target of Rapamycin Attenuates Cardiomyopathies in Adult Zebrafish

Authors
Ding, Y., Sun, X., Huang, W., Hoage, T., Redfield, M., Kushwaha, S., Sivasubbu, S., Lin, X., Ekker, S., and Xu, X.
ID
ZDB-PUB-110719-26
Date
2011
Source
Circulation research   109(6): 658-69 (Journal)
Registered Authors
Ding, Yonghe, Ekker, Stephen C., Hoage, Tiffany R., Huang, Wei, Lin, Xueying, Sivasubbu, Sridhar, Sun, Xiaojing, Xu, Xiaolei
Keywords
doxorubicin, cardiotoxicity, cardiomyopathy, target of rapamycin, zebrafish, anemia
MeSH Terms
  • Aging/genetics*
  • Animals
  • Animals, Genetically Modified
  • Cardiomyopathies/enzymology*
  • Cardiomyopathies/genetics*
  • Cardiomyopathies/prevention & control
  • Cells, Cultured
  • Disease Models, Animal
  • Haploinsufficiency/genetics*
  • TOR Serine-Threonine Kinases/biosynthesis
  • TOR Serine-Threonine Kinases/deficiency*
  • TOR Serine-Threonine Kinases/genetics*
  • Zebrafish
  • Zebrafish Proteins/biosynthesis
  • Zebrafish Proteins/deficiency*
  • Zebrafish Proteins/genetics*
PubMed
21757652 Full text @ Circ. Res.
Abstract

Rationale: Although a cardioprotective function of target of rapamycin (TOR) signaling inhibition has been suggested by pharmacological studies using rapamycin, genetic evidences are still lacking. We explored adult zebrafish as a novel vertebrate model for dissecting signaling pathways in cardiomyopathy.

Objective: We generated the second adult zebrafish cardiomyopathy model induced by doxorubicin. By genetically analyzing both the doxorubicin and our previous established anemia-induced cardiomyopathy models, we decipher the functions of TOR signaling in cardiomyopathies of different etiology.

Methods and Results: Along the progression of both cardiomyopathy models, we detected dynamic TOR activity at different stages of pathogenesis as well as distinct effects of TOR signaling inhibition. Nevertheless, cardiac enlargement in both models can be effectively attenuated by inhibition of TOR signaling through short-term rapamycin treatment. To assess the long-term effects of TOR reduction, we used a zebrafish target of rapamycin (ztor) mutant identified from an insertional mutagenesis screen. We show that TOR haploinsufficiency in the ztor heterozygous fish improved cardiac function, prevented pathological remodeling events, and ultimately reduced mortality in both adult fish models of cardiomyopathy. Mechanistically, these cardioprotective effects are conveyed by the antihypertrophy, antiapoptosis, and proautophagy function of TOR signaling inhibition.

Genes / Markers
Figures
Expression
Phenotype
Mutation and Transgenics
Human Disease / Model Data
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping
Errata and Notes