Department of Ophthalmology, UCSF Medical Center, University of California San Francisco, San Francisco, CA, USA.
Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California San Francisco, San Francisco, CA, USA.
Transl Vis Sci Technol. 2022 Nov 1;11(11):17. doi: 10.1167/tvst.11.11.17.
The cone-dominant, 13-lined ground squirrel (13-LGS) retina mimics the human central retina, but a thorough examination of retinal development in this species has not been reported. Here, the embryonic and postnatal development of the 13-LGS retina was studied to further characterize 13-LGS as a practical alternative animal model for investigating cone-based vision in health and disease.
The spatiotemporal expression of key progenitor and cell type markers was examined in retinas from defined embryonic and postnatal stages using immunohistochemistry. Postnatal gene expression changes were validated by quantitative PCR.
The 13-LGS neuroblastic layer expressed key progenitor markers (Sox2, Vsx2, Pax6, and Lhx2) at E18. Sequential cell fate determination evidenced by the first appearance of cell-type-specific marker labeling was at embryonic stage 18 (E18) with ganglion cells (Brn-3A, HuC/D) and microglia (Iba1); at E22.5 with photoreceptor progenitors (Otx2, recoverin) followed shortly by horizontal and amacrine cells (Lhx1, Oc1) at E24 to E25.5; and at postnatal stage 15 (P15) with bipolar cells (Vsx1, CaBP5) and Müller glia cells (GS, Rlbp1). Photoreceptor maturation indicated by opsin-positive outer segments and peanut agglutinin (PNA) labeling of cone sheaths was completed at the time of eye opening (P21-P24).
The timeline and order of retinal cell development in the 13-LGS generally matches that recorded from other mammalian models but with a stark variation in the proportion of various cell types due to cone-dense photoreceptors.
This thorough examination of an emerging translationally relevant cone-dominant specie provides a baseline for future disease modeling and stem cell approach studies of human vision.
圆锥主导的 13 行地松鼠(13-LGS)视网膜模拟人类中央视网膜,但该物种视网膜发育的全面研究尚未报道。在这里,研究了 13-LGS 视网膜的胚胎和出生后发育,以进一步将 13-LGS 确定为研究健康和疾病中基于视锥的视觉的实用替代动物模型。
使用免疫组织化学检查来自特定胚胎和出生后阶段的视网膜中关键祖细胞和细胞类型标记物的时空表达。通过定量 PCR 验证了出生后基因表达的变化。
13-LGS 神经母细胞层在 E18 时表达关键祖细胞标记物(Sox2、Vsx2、Pax6 和 Lhx2)。通过首次出现细胞类型特异性标记物标记来证明细胞命运的顺序决定,发生在胚胎阶段 18(E18),此时出现了神经元细胞(Brn-3A、HuC/D 和小胶质细胞(Iba1);在 E22.5 时出现了光感受器祖细胞(Otx2、恢复蛋白),随后在 E24 至 E25.5 时出现了水平细胞和无长突细胞(Lhx1、Oc1);在出生后阶段 15(P15)时出现了双极细胞(Vsx1、CaBP5)和 Müller 胶质细胞(GS、Rlbp1)。光感受器成熟的标志是视蛋白阳性的外节和花生凝集素(PNA)标记的锥体鞘在眼睛睁开时(P21-P24)完成。
13-LGS 视网膜细胞发育的时间和顺序通常与其他哺乳动物模型记录的相似,但由于视锥密集的光感受器,各种细胞类型的比例存在明显差异。
这项对新兴转化相关的圆锥主导物种的全面检查为未来的疾病建模和人类视觉的干细胞方法研究提供了一个基线。