Suleiman Hani, Zhang Lei, Roth Robyn, Heuser John E, Miner Jeffrey H, Shaw Andrey S, Dani Adish
Department of Pathology and Immunology , Washington University School of Medicine , St. Louis , United States.
Elife. 2013 Oct 8;2:e01149. doi: 10.7554/eLife.01149.
In multicellular organisms, proteins of the extracellular matrix (ECM) play structural and functional roles in essentially all organs, so understanding ECM protein organization in health and disease remains an important goal. Here, we used sub-diffraction resolution stochastic optical reconstruction microscopy (STORM) to resolve the in situ molecular organization of proteins within the kidney glomerular basement membrane (GBM), an essential mediator of glomerular ultrafiltration. Using multichannel STORM and STORM-electron microscopy correlation, we constructed a molecular reference frame that revealed a laminar organization of ECM proteins within the GBM. Separate analyses of domains near the N- and C-termini of agrin, laminin, and collagen IV in mouse and human GBM revealed a highly oriented macromolecular organization. Our analysis also revealed disruptions in this GBM architecture in a mouse model of Alport syndrome. These results provide the first nanoscopic glimpse into the organization of a complex ECM. DOI:http://dx.doi.org/10.7554/eLife.01149.001.
在多细胞生物中,细胞外基质(ECM)的蛋白质在几乎所有器官中都发挥着结构和功能作用,因此了解健康和疾病状态下ECM蛋白质的组织情况仍然是一个重要目标。在这里,我们使用亚衍射分辨率随机光学重建显微镜(STORM)来解析肾肾小球基底膜(GBM)内蛋白质的原位分子组织,GBM是肾小球超滤的重要介质。通过多通道STORM和STORM-电子显微镜关联分析,我们构建了一个分子参考框架,揭示了GBM内ECM蛋白质的层状组织。对小鼠和人类GBM中聚集蛋白、层粘连蛋白和IV型胶原蛋白的N端和C端附近结构域的单独分析揭示了一种高度定向的大分子组织。我们的分析还揭示了在阿尔波特综合征小鼠模型中这种GBM结构的破坏。这些结果首次提供了对复杂ECM组织的纳米级观察。DOI:http://dx.doi.org/10.7554/eLife.01149.001 。