首页> 外文期刊>Journal of Molecular Neuroscience: MN >Increased TRPV4 expression in urinary bladder and lumbosacral dorsal root ganglia in mice with chronic overexpression of NGF in urothelium
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Increased TRPV4 expression in urinary bladder and lumbosacral dorsal root ganglia in mice with chronic overexpression of NGF in urothelium

机译:慢性尿路上皮NGF过​​度表达的小鼠膀胱和腰ac背根神经节TRPV4表达增加

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Transient receptor potential vanilloid (TRPV) family member 4 (TRPV4) expression has been demonstrated in urothelial cells and dorsal root ganglion (DRG) neurons, and roles in normal micturition reflexes as well as micturition dysfunction have been suggested. TRP channel expression and function is dependent upon target tissue expression of growth factors. These studies expand upon the target tissue dependence of TRPV4 expression in the urinary bladder and lumbosacral DRG using a recently characterized transgenic mouse model with chronic overexpression of nerve growth factor (NGF-OE) in the urothelium. Immunohistochemistry with image analyses, real-time quantitative polymerase chain reaction, and Western blotting were used to determine TRPV4 protein and transcript expression in the urinary bladder (urothelium + suburothelium, detrusor) and lumbosacral DRG from littermate wild-type (WT) and NGF-OE mice. Antibody specificity controls were performed in TRPV4-/- mice. TRPV4 transcript and protein expression was significantly (p ≤ 0.001) increased in the urothelium + suburothelium and suburothelial nerve plexus of the urinary bladder and in small- and medium-sized lumbosacral (L1, L2, L6-S1) DRG cells from NGF-OE mice compared to littermate WT mice. NGF-OE mice exhibit significant (p ≤ 0.001) increases in NGF transcript and protein in the urothelium + suburothelium and lumbosacral DRG. These studies demonstrate regulation of TRPV4 expression by NGF in lower urinary tract tissues. Ongoing studies are characterizing the functional roles of TRPV4 expression in the sensory limb (DRG, urothelium) of the micturition reflex.
机译:已在尿路上皮细胞和背根神经节(DRG)神经元中证明了瞬时受体电位香草酸(TRPV)家族成员4(TRPV4)的表达,并已提出在正常排尿反射以及排尿功能障碍中的作用。 TRP通道的表达和功能取决于生长因子的靶组织表达。这些研究使用最近表征的在尿路上皮中神经生长因子(NGF-OE)长期过度表达的转基因小鼠模型扩展了膀胱和腰sDRG中TRPV4表达的靶组织依赖性。免疫组织化学与图像分析,实时定量聚合酶链反应和Western印迹法用于确定TRPV4蛋白和转录本在膀胱(尿路上皮+尿路上皮下,逼尿肌)和腰lit DRG中来自同窝野生型(WT)和NGF-的表达OE小鼠。在TRPV4-/-小鼠中进行抗体特异性对照。 NGF-OE产生的膀胱上皮+上皮下神经丛和尿路上皮下神经丛以及中小型腰((L1,L2,L6-S1)DRG细胞中TRPV4转录和蛋白表达显着增加(p≤0.001)小鼠与同窝的WT小鼠相比。 NGF-OE小鼠的尿路上皮+尿路上皮下和腰s背DRG中的NGF转录和蛋白质显着增加(p≤0.001)。这些研究表明NGF在下尿路组织中调节TRPV4表达。正在进行的研究表征了TRPV4表达在排尿反射的感觉肢体(DRG,尿路上皮)中的功能作用。

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