Moran Eye Center, University of Utah Department of Ophthalmology and Visual Sciences, 65 Mario Capecchi Drive, Salt Lake City, UT 84132, USA.
Moran Eye Center, University of Utah Department of Ophthalmology and Visual Sciences, 65 Mario Capecchi Drive, Salt Lake City, UT 84132, USA; Signature Immunologics, Torrey, UT, USA.
Trends Endocrinol Metab. 2020 Apr;31(4):320-329. doi: 10.1016/j.tem.2020.01.005. Epub 2020 Feb 24.
Müller cells are glia that play important regulatory roles in retinal metabolism. These roles have been evolutionarily conserved across at least 300 million years. Müller cells have a tightly locked metabolic signature in the healthy retina, which rapidly degrades in response to insult and disease. This variation in metabolic signature occurs in a chaotic fashion, involving some central metabolic pathways. The cause of this divergence of Müller cells, from a single class with a unique metabolic signature to numerous separable metabolic classes, is currently unknown and illuminates potential alternative metabolic pathways that may be revealed in disease. Understanding the impacts of this heterogeneity on degenerate retinas and the implications for the metabolic support of surrounding neurons will be critical to long-term integration of retinal therapeutics for the restoration of visual perception following photoreceptor degeneration.
Müller 细胞是神经胶质细胞,在视网膜代谢中发挥重要的调节作用。这些作用在至少 3 亿年的进化过程中是保守的。Müller 细胞在健康的视网膜中有一个紧密锁定的代谢特征,当受到损伤和疾病的影响时,这个特征会迅速降解。这种代谢特征的变化是混乱的,涉及一些中心代谢途径。目前还不知道是什么原因导致 Müller 细胞从具有独特代谢特征的单一类型细胞分化为众多可分离的代谢类型,这揭示了在疾病中可能出现的潜在替代代谢途径。了解这种异质性对退化视网膜的影响,以及对周围神经元代谢支持的影响,对于长期整合视网膜治疗以恢复光感受器退化后的视觉感知至关重要。