Department of Molecular and Cellular Biology, Harvard University, Cambridge, MA 02138;
Department of Ophthalmology and Visual Sciences, Moran Eye Center, University of Utah School of Medicine, Salt Lake City, UT 84132.
Proc Natl Acad Sci U S A. 2020 Aug 4;117(31):18780-18787. doi: 10.1073/pnas.2011532117. Epub 2020 Jul 22.
Macular telangiectasia type 2 (MacTel), a late-onset macular degeneration, has been linked to a loss in the retina of Müller glial cells and the amino acid serine, synthesized by the Müller cells. The disease is confined mainly to a central retinal region called the MacTel zone. We have used electron microscopic connectomics techniques, optimized for disease analysis, to study the retina from a 48-y-old woman suffering from MacTel. The major observations made were specific changes in mitochondrial structure within and outside the MacTel zone that were present in all retinal cell types. We also identified an abrupt boundary of the MacTel zone that coincides with the loss of Müller cells and macular pigment. Since Müller cells synthesize retinal serine, we propose that a deficiency of serine, required for mitochondrial maintenance, causes mitochondrial changes that underlie MacTel development.
2 型黄斑毛细血管扩张症(MacTel)是一种迟发性黄斑变性,与视网膜 Müller 胶质细胞和由 Müller 细胞合成的氨基酸丝氨酸的丧失有关。这种疾病主要局限于一个称为 MacTel 区的中央视网膜区域。我们使用了针对疾病分析进行了优化的电子显微镜连接组学技术,来研究一位 48 岁患有 MacTel 的女性的视网膜。主要观察结果是,在 MacTel 区内外,所有视网膜细胞类型的线粒体结构都发生了特定变化。我们还确定了 MacTel 区的一个突然边界,该边界与 Müller 细胞和黄斑色素的丧失相吻合。由于 Müller 细胞合成视网膜丝氨酸,我们提出,维持线粒体所需的丝氨酸缺乏会导致线粒体变化,从而导致 MacTel 的发展。