Strettoi Enrica
Italian National Research Council, Neuroscience Institute Pisa, Italy.
Front Cell Neurosci. 2015 Dec 23;9:494. doi: 10.3389/fncel.2015.00494. eCollection 2015.
Up to 15 years ago, bibliographic searches based on keywords such as "photoreceptor degeneration, inner retina" or "photoreceptor degeneration, second order neurons" returned only a handful of papers, as the field was dominated by the general assumption that retinal degeneration had direct effects on the sole populations of rods and cones. Since then, a number of studies have been dedicated to understanding the process of gradual morphological, molecular, and functional changes arising among cells located in the inner retina (comprising neurons, glia, and blood vessels), that is to say "beyond" photoreceptors. General aspects of this progression of biological rearrangements, now referred to as "remodeling", were revealed and demonstrated to accompany consistently photoreceptor loss, independently from the underlying cause of degeneration. Recurrent features of remodeling are summarized here, to provide a general frame for to the various analytical descriptions and reviews contributed by the articles in the issue (among others, see Euler and Schubert, 2015; Soto and Kerschensteiner, 2015, this issue).
直到15年前,基于“光感受器退化,视网膜内层”或“光感受器退化,二级神经元”等关键词的文献检索只能找到寥寥几篇论文,因为当时该领域普遍认为视网膜退化只会直接影响视杆细胞和视锥细胞这两类细胞。从那时起,许多研究致力于了解视网膜内层(包括神经元、神经胶质细胞和血管)细胞中逐渐出现的形态、分子和功能变化过程,也就是说,这些变化发生在光感受器“之外”。现在被称为“重塑”的这种生物重排过程的一般特征已被揭示,并被证明始终伴随着光感受器的丧失,且与退化的潜在原因无关。本文总结了重塑的反复出现的特征,为本期文章(包括但不限于Euler和Schubert,2015年;Soto和Kerschensteiner,2015年,本期)所做的各种分析描述和综述提供一个总体框架。