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A novel contractile phenotype with cardiac transgenic expression of the human P2X 4 receptor
Author(s) -
Hu Bing,
Mei Qi-Bing,
Yao Xiu-Juan,
Smith Emily,
Barry William H.,
Liang Bruce T.
Publication year - 2001
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fj.01-0445fje
Subject(s) - contractility , receptor , medicine , endocrinology , biology , myocyte , cardiac function curve , cardiac myocyte , transgene , agonist , heart failure , biochemistry , gene
The P2X 4 receptor is a newly identified receptor expressed in the heart cell. Its function was elucidated with cardiac transgenic (TG) expression of the receptor by using the myocardium‐specific α‐myosin heavy chain promoter. The presence of the transgene was determined by polymerase chain reaction by using primers specific to the receptor and the vector linker region, by Southern blotting of the genomic DNA, and by immunoblotting and immunohistochemistry of both isolated cardiac myocytes and intact hearts. In intact heart study, the P2X 4 receptor TG mouse exhibited significantly elevated basal cardiac contractility with greater rates of contraction and relaxation, left ventricular developed pressure, and cardiac output compared with nontransgenic (NTG) animals but showed no evidence of hypertrophy or heart failure. The TG heart also showed a greater increase of cardiac contractility in response to the P2X receptor agonist 2‐methylthioATP, consistent with overexpression of a functional P2X 4 receptor with consequent increase in the receptor‐mediated response. In isolated cardiac cell study, the TG heart cell showed a similar level of basal contraction amplitude as the NTG heart cell while exhibiting a threefold greater increase in contractility during stimulation by 2‐methylthioATP. Thus, an increased responsiveness of the overexpressed P2X 4 receptor to endogenous ATP is responsible for the enhanced basal cardiac performance in the intact TG heart. The sustained enhanced contractile function with no associated heart pathology in the P2X 4 receptor TG mouse suggests a novel physiologic role of the P2X 4 receptor, that of stimulating the cardiac contractility.