Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Core Facility for Integrated Microscopy, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
Am J Physiol Renal Physiol. 2020 Mar 1;318(3):F732-F740. doi: 10.1152/ajprenal.00185.2019. Epub 2020 Jan 27.
Renal autoregulation is mediated by the myogenic response and tubuloglomerular feedback (TGF) working in concert to maintain renal blood flow and glomerular filtration rate despite fluctuations in renal perfusion pressure. Intercellular communication through gap junctions may play a role in renal autoregulation. We examine if one of the building blocks in gap junctions, connexin45 (Cx45), which is expressed in vascular smooth muscle cells, has an influence on renal autoregulatory efficiency. The isolated perfused juxtamedullary nephron preparation was used to measure afferent arteriolar diameter changes in response to acute changes in renal perfusion pressure. In segmental arteries, pressure myography was used to study diameter changes in response to pressure changes. Wire myography was used to study vasoconstrictor and vasodilator responses. A mathematical model of the vascular wall was applied to interpret experimental data. We found a significant reduction in the afferent arteriolar constriction in response to acute pressure increases in Cx45 knockout (KO) mice compared with wild-type (WT) mice. Abolition of TGF caused a parallel upward shift in the autoregulation curve of WT animals but had no effect in KO animals, which is compatible with TGF providing a basal tonic contribution in afferent arterioles whereas Cx45 KO animals were functionally papillectomized. Analysis showed a shift toward lower stress sensitivity in afferent arterioles from Cx45 KO animals, indicating that the absence of Cx45 may also affect myogenic properties. Finally, loss of Cx45 in vascular smooth muscle cells appeared to associate with a change in both structure and passive properties of the vascular wall.
肾自身调节是通过肌源性反应和管球反馈(TGF)协同作用来实现的,旨在维持肾血流量和肾小球滤过率,尽管肾灌注压波动。细胞间通过缝隙连接的通讯可能在肾自身调节中发挥作用。我们研究了缝隙连接的一个组成部分,即血管平滑肌细胞中表达的连接蛋白 45(Cx45),是否对肾自身调节效率有影响。使用分离的髓质近球肾单位灌注制备来测量入球小动脉直径对肾灌注压急性变化的反应。在节段性动脉中,压力描记术用于研究直径对压力变化的反应。线描记术用于研究血管收缩和舒张反应。应用血管壁的数学模型来解释实验数据。我们发现,与野生型(WT)小鼠相比,Cx45 敲除(KO)小鼠的入球小动脉对急性压力升高的收缩反应明显减弱。TGF 的消除导致 WT 动物的自身调节曲线平行向上移位,但对 KO 动物没有影响,这与 TGF 在入球小动脉中提供基础紧张贡献相一致,而 Cx45 KO 动物在功能上被切除了乳头。分析表明,Cx45 KO 动物的入球小动脉的应激敏感性向较低值转移,表明 Cx45 的缺失也可能影响肌源性特性。最后,血管平滑肌细胞中 Cx45 的缺失似乎与血管壁的结构和被动特性的改变有关。