Impaired platelet-derived growth factor receptor expression and function in cultured lower esophageal sphincter circular smooth muscle cells from W/Wv mutant mice

被引:4
作者
Bautista-Cruz, Francisco [1 ]
Nair, Dileep G. [1 ,2 ]
Lourenssen, Sandra [1 ]
Miller, David V. [1 ]
Blennerhassett, Michael G. [1 ,2 ,3 ]
Paterson, William G. [1 ,2 ,3 ]
机构
[1] Kingston Gen Hosp, Gastrointestinal Dis Res Unit, Kingston, ON K7L 2V7, Canada
[2] Queens Univ, Dept Biomed & Mol Sci, Kingston, ON K7L 3N6, Canada
[3] Queens Univ, Dept Med, Dept Biol, Kingston, ON K7L 3N6, Canada
基金
加拿大健康研究院;
关键词
PDGF; calcium imaging; smooth muscle cells; esophagus; sphincter; interstitial cells of Cajal; INTERSTITIAL-CELLS; SIGNAL-TRANSDUCTION; IN-VIVO; INHIBITORY NEUROTRANSMISSION; NEUROMUSCULAR-TRANSMISSION; PDGF RECEPTORS; NITRIC-OXIDE; CAJAL; DIFFERENTIATION; GUT;
D O I
10.1139/cjpp-2013-0254
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We have previously demonstrated that lower esophageal sphincter (LES) circular smooth muscle (CSM) is functionally impaired in W/W-v mutant mice that lack interstitial cells of Cajal, and speculated that this could be due to altered smooth muscle differentiation. Platelet-derived growth factor (PDGF) is involved in the maturation and differentiation of smooth muscle. To determine whether PDGF expression and (or) function is altered in W/W-v mutant mice, PDGF-R beta expression was measured using RT-PCR, qPCR, and immunocytochemistry, and Ca2+ imaging and perforated patch clamp recordings performed in isolated LES CSM cells. RT-PCR and immunocytochemistry showed significantly reduced PDGF-R beta expression in the LES from mutant as opposed to wild-type mice. Quantitative comparison of CSM cell numbers in histological specimens revealed a significantly increased average cell size in the mutant tissue. The specific PDGF-R beta ligand, PDGF-BB, caused a significant increase in intracellular Ca2+ in cells from the wild-type mice compared with the mutants. Using a ramp protocol, PDGF-BB caused a 2-fold increase in outward K+ currents in cells from the wild-type mice, whereas no significant increase was measured in the cells from the mutants. We conclude that the expression and function of PDGF-R beta in LES CSM from W/W-v mice is impaired, providing further evidence that LES CSM is abnormal in W/W-v mutants.
引用
收藏
页码:34 / 41
页数:8
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