Boys Town National Research Hospital, Omaha, NE, USA.
Oregon Health Science Center, Portland, OR, USA.
Hear Res. 2020 May;390:107935. doi: 10.1016/j.heares.2020.107935. Epub 2020 Mar 18.
In 129 Sv autosomal Alport mice, the strial capillary basement membranes (SCBMs) progressively thicken between 5 and 9 weeks of age resulting in a hypoxic microenvironment with metabolic stress and induction of pro-inflammatory cytokines and chemokines. These events occur concomitant with a drop in endocochlear potential and a susceptibility to noise-induced hearing loss under conditions that do not permanently affect age/strain-matched littermates. Here we aimed to gain an understanding of events that occur before the onset of SCBM thickening. Alport stria has normal thickness and shows levels of extracellular matrix (ECM) molecules in the SCBMs commensurate with wild-type mice. Hearing thresholds in the 3-week Alport mice do not differ from those of wild-type mice. We performed RNAseq analysis using RNA from stria vascularis isolated from 3-week Alport mice and wild type littermates. Data was processed using Ingenuity Pathway Analysis software and further distilled using manual procedures. RNAseq analysis revealed significant dysregulation of genes involved in cell adhesion, cell migration, formation of protrusions, and both actin and tubulin cytoskeletal dynamics. Overall, the data suggested changes in the cellular architecture of the stria might be apparent. To test this notion, we performed dual immunofluorescence analysis on whole mounts of the stria vascularis from these same animals stained with anti-isolectin gs-ib4 (endothelial cell marker) and anti-desmin (pericyte marker) antibodies. The results showed evidence of pericyte detachment and migration as well as the formation of membrane ruffling on pericytes in z-stacked confocal images from Alport mice compared to wild type littermates. This was confirmed by TEM analysis. Earlier work from our lab showed that endothelin A receptor blockade prevents SCBM thickening and ECM accumulation in the SCBMs. Treating cultured pericytes with endothelin-1 induced actin cytoskeletal rearrangement, increasing the ratio of filamentous to globular actin. Collectively, these findings suggest that the change in type IV collagen composition in the Alport SCBMs results in cellular insult to the pericyte compartment, activating detachment and altered cytoskeletal dynamics. These events precede SCBM thickening and hearing loss in Alport mice, and thus constitute the earliest event so far recognized in Alport strial pathology.
在 129Sv 常染色体 Alport 小鼠中,纹状血管基底膜(SCBM)在 5 至 9 周龄之间逐渐增厚,导致缺氧微环境,伴有代谢应激和促炎细胞因子和趋化因子的诱导。这些事件发生的同时,内淋巴液电位下降,并且在不永久影响年龄/品系匹配的同窝仔鼠的情况下,易发生噪声性听力损失。在这里,我们旨在了解 SCBM 增厚前发生的事件。Alport 纹状体内的纹状突具有正常的厚度,并显示出与野生型小鼠相当的 SCBM 中细胞外基质(ECM)分子的水平。3 周龄 Alport 小鼠的听力阈值与野生型小鼠没有差异。我们使用从 3 周龄 Alport 小鼠和野生型同窝仔鼠分离的血管纹组织中的 RNA 进行 RNAseq 分析。使用 Ingenuity Pathway Analysis 软件处理数据,并使用手动程序进一步进行提取。RNAseq 分析显示,参与细胞黏附、细胞迁移、突起形成以及肌动蛋白和微管细胞骨架动力学的基因显著失调。总的来说,数据表明纹状突的细胞结构可能发生明显变化。为了验证这一观点,我们对来自这些相同动物的血管纹的全培养物进行了双重免疫荧光分析,用抗异凝集素 gs-ib4(内皮细胞标记物)和抗结蛋白(周细胞标记物)抗体染色。与野生型同窝仔鼠相比,Alport 小鼠的 z 堆叠共聚焦图像显示,周细胞出现了分离和迁移的证据,以及周细胞上的膜皱襞形成。这一结果通过 TEM 分析得到了证实。我们实验室的早期工作表明,内皮素 A 受体阻断可防止 SCBM 增厚和 ECM 在 SCBM 中的积累。用内皮素-1 处理培养的周细胞可诱导肌动蛋白细胞骨架重排,增加丝状肌动蛋白与球状肌动蛋白的比例。总的来说,这些发现表明,Alport SCBM 中 IV 型胶原组成的改变导致周细胞区室受到细胞损伤,激活分离和改变细胞骨架动力学。这些事件发生在 Alport 小鼠的 SCBM 增厚和听力损失之前,因此构成了迄今为止在 Alport 纹状体病理学中最早识别的事件。