Shaw Peter X, Fang Jiahua, Sang Alan, Wang Yan, Kapiloff Michael S, Goldberg Jeffrey L
Department of Ophthalmology, University of California San Diego, La Jolla, California, United States.
Department of Ophthalmology, University of California San Diego, La Jolla, California, United States 2Department of Ophthalmology, First Hospital of Changsha, Changsha, Hunan Province, China.
Invest Ophthalmol Vis Sci. 2016 Sep 1;57(11):5083-5092. doi: 10.1167/iovs.16-19465.
We have previously demonstrated that soluble adenylyl cyclase (sAC) is necessary for retinal ganglion cell (RGC) survival and axon growth. Here, we further investigate the role of sAC in neuronal differentiation during retinal development.
Chx10 or Math5 promoter-driven Cre-Lox recombination were used to conditionally delete sAC from early and intermediate retinal progenitor cells during retinal development. We examined cell type-specific markers expressed by retinal cells to estimate their relative numbers and characterize retinal laminar morphology by immunofluorescence in adult and newborn mice.
Retinal ganglion cell and amacrine cell markers were significantly lower in the retinas of adult Math5cre/sACfl/fl and Chx10cre/sACfl/fl mice than in those of wild-type controls. The effect on RGC development was detectable as early as postnatal day 1 and deleting sAC in either Math5- or Chx10-expressing retinal progenitor cells also reduced nerve fiber layer thickness into adulthood. The thickness of the photoreceptor layer was slightly but statistically significantly decreased in both the newborn Chx10cre/sACfl/fl and Math5cre/sACfl/fl mice, but this reduction and abnormal morphology persisted in the adults in only the Chx10cre/sACfl/fl mice.
sAC plays an important role in the early retinal development of RGCs as well as in the development of amacrine cells and to a lesser degree photoreceptors.
我们之前已经证明可溶性腺苷酸环化酶(sAC)对视网膜神经节细胞(RGC)的存活和轴突生长是必需的。在此,我们进一步研究sAC在视网膜发育过程中神经元分化中的作用。
利用Chx10或Math5启动子驱动的Cre-Lox重组,在视网膜发育过程中从早期和中期视网膜祖细胞中条件性删除sAC。我们检测了视网膜细胞表达的细胞类型特异性标志物,以估计它们的相对数量,并通过免疫荧光法对成年和新生小鼠的视网膜层形态进行表征。
成年Math5cre/sACfl/fl和Chx10cre/sACfl/fl小鼠视网膜中的视网膜神经节细胞和无长突细胞标志物明显低于野生型对照。对RGC发育的影响早在出生后第1天就可检测到,并且在表达Math5或Chx10的视网膜祖细胞中删除sAC也会导致成年后神经纤维层厚度降低。新生Chx10cre/sACfl/fl和Math5cre/sACfl/fl小鼠的光感受器层厚度均略有下降,但具有统计学意义,不过只有Chx10cre/sACfl/fl小鼠的这种厚度降低和形态异常在成年后仍然存在。
sAC在RGC的早期视网膜发育以及无长突细胞的发育中起重要作用,对光感受器的作用程度较小。