Department of Anatomy and Developmental Biology, School of Biomedical Sciences, Faculty of Medicine, Nursing and Health Sciences, Monash University, Clayton, Victoria, Australia.
Liverpool Ocular Oncology Research Group, Department of Molecular and Clinical Cancer Medicine, Institute of Translational Medicine, University of Liverpool, Liverpool, United Kingdom.
Invest Ophthalmol Vis Sci. 2020 Aug 3;61(10):33. doi: 10.1167/iovs.61.10.33.
Human choroidal melanocytes become evident in the last trimester of development, but very little is known about them. To better understand normal and diseased choroidal melanocyte biology we examined their precursors, melanoblasts (MB), in mouse eyes during development, particularly their relation to the developing vasculature and immune cells.
Naïve B6(Cg)-Tyrc-2J/J albino mice were used between embryonic (E) day 15.5 and postnatal (P) day 8, with adult controls. Whole eyes, posterior segments, or dissected choroidal wholemounts were stained with antibodies against tyrosinase-related protein 2, ionized calcium binding adaptor molecule-1 or isolectin B4, and examined by confocal microscopy. Immunoreactive cell numbers in the choroid were quantified with Imaris. One-way ANOVA with Tukey's post hoc test assessed statistical significance.
Small numbers of MB were present in the presumptive choroid at E15.5 and E18.5. The density significantly increased between E18.5 (381.4 ± 45.8 cells/mm2) and P0 (695.2 ± 87.1 cells/mm2; P = 0.032). In postnatal eyes MB increased in density and formed multiple layers beneath the choriocapillaris. MB in the periocular mesenchyme preceded the appearance of vascular structures at E15.5. Myeloid cells (Ionized calcium binding adaptor molecule-1-positive) were also present at high densities from this time, and attained adult-equivalent densities by P8 (556.4 ± 73.6 cells/mm2).
We demonstrate that choroidal MB and myeloid cells are both present at very early stages of mouse eye development (E15.5). Although MB and vascularization seemed to be unlinked early in choroidal development, they were closely associated at later stages. MB did not migrate into the choroid in waves, nor did they have a consistent relationship with nerves.
人类脉络膜黑素细胞在发育的最后一个 trimester 中变得明显,但对它们知之甚少。为了更好地了解正常和患病的脉络膜黑素细胞生物学,我们在发育过程中检查了小鼠眼睛中的前体细胞-黑素细胞前体(MB),特别是它们与发育中的脉管系统和免疫细胞的关系。
在胚胎(E)第 15.5 天至出生后(P)第 8 天之间使用 B6(Cg)-Tyrc-2J/J 白化鼠,并用成年对照。用针对酪氨酸酶相关蛋白 2、离子钙结合衔接蛋白 1 或同工凝集素 B4 的抗体对整个眼睛、后段或解剖的脉络膜全层进行染色,并通过共聚焦显微镜检查。用 Imaris 定量分析脉络膜中的免疫反应性细胞数量。采用单因素方差分析和 Tukey 事后检验评估统计学意义。
在 E15.5 和 E18.5 时,假定脉络膜中存在少量的 MB。密度在 E18.5(381.4±45.8 个细胞/mm2)和 P0(695.2±87.1 个细胞/mm2;P=0.032)之间显著增加。在出生后的眼睛中,MB 的密度增加,并在脉络膜毛细血管下形成多层。E15.5 时,眼周间充质中的 MB 先于血管结构的出现。从那时起,髓样细胞(离子钙结合衔接蛋白 1 阳性)也以高浓度存在,并在 P8 时达到成年等效密度(556.4±73.6 个细胞/mm2)。
我们证明了脉络膜 MB 和髓样细胞在小鼠眼睛发育的早期阶段(E15.5)就已经存在。虽然在脉络膜发育的早期,MB 和血管似乎没有联系,但在后期它们紧密相关。MB 不是以波的形式迁移到脉络膜中,也没有与神经保持一致的关系。