Schepens Eye Research Institute, Mass. Eye and Ear, Boston, MA, USA.
Department of Biomedical Engineering, Boston University, Boston, MA, USA.
J Cell Mol Med. 2017 Oct;21(10):2542-2552. doi: 10.1111/jcmm.13175. Epub 2017 Apr 12.
The retinal pigment epithelium located between the neurosensory retina and the choroidal vasculature is critical for the function and maintenance of both the photoreceptors and underlying capillary endothelium. While the trophic role of retinal pigment epithelium on choroidal endothelial cells is well recognized, the existence of a reciprocal regulatory function of endothelial cells on retinal pigment epithelium cells remained to be fully characterized. Using a physiological long-term co-culture system, we determined the effect of retinal pigment epithelium-endothelial cell heterotypic interactions on cell survival, behaviour and matrix deposition. Human retinal pigment epithelium and endothelial cells were cultured on opposite sides of polyester transwells for up to 4 weeks in low serum conditions. Cell viability was quantified using a trypan blue assay. Cellular morphology was evaluated by H&E staining, S.E.M. and immunohistochemistry. Retinal pigment epithelium phagocytic function was examined using a fluorescent bead assay. Gene expression analysis was performed on both retinal pigment epithelium and endothelial cells by quantitative PCR. Quantification of extracellular matrix deposition was performed on decellularized transwells stained for collagen IV, fibronectin and fibrillin. Our results showed that presence of endothelial cells significantly improves retinal pigment epithelium maturation and function as indicated by the induction of visual cycle-associated genes, accumulation of a Bruch's membrane-like matrix and increase in retinal pigment epithelium phagocytic activity. Co-culture conditions led to increased expression of anti-angiogenic growth factors and receptors in both retinal pigment epithelium and endothelial cells compared to monoculture. Tube-formation assays confirmed that co-culture with retinal pigment epithelium significantly decreased the angiogenic phenotype of endothelial cells. These findings provide evidence of critical interdependent interactions between retinal pigment epithelium and endothelial cell involved in the maintenance of retinal homeostasis.
位于神经感觉视网膜和脉络膜血管之间的视网膜色素上皮对于光感受器和其下方毛细血管内皮的功能和维持都至关重要。虽然视网膜色素上皮对脉络膜内皮细胞的营养作用已得到充分认识,但内皮细胞对视网膜色素上皮细胞的反向调节功能仍有待充分描述。我们使用生理长期共培养系统,确定了视网膜色素上皮-内皮细胞异质相互作用对细胞存活、行为和基质沉积的影响。将人视网膜色素上皮和内皮细胞培养在聚酯 Transwell 的相对两侧,在低血清条件下培养长达 4 周。使用台盼蓝测定法定量测定细胞活力。通过 H&E 染色、SEM 和免疫组织化学评估细胞形态。使用荧光珠测定法检查视网膜色素上皮的吞噬功能。通过定量 PCR 对视网膜色素上皮和内皮细胞进行基因表达分析。对脱细胞 Transwell 进行胶原 IV、纤连蛋白和原纤维蛋白染色,以定量测定细胞外基质沉积。我们的结果表明,内皮细胞的存在显著改善了视网膜色素上皮的成熟和功能,表现为视觉循环相关基因的诱导、Bruch 膜样基质的积累和视网膜色素上皮吞噬活性的增加。与单培养相比,共培养条件导致视网膜色素上皮和内皮细胞中抗血管生成生长因子和受体的表达增加。管形成测定证实,与视网膜色素上皮共培养显著降低了内皮细胞的血管生成表型。这些发现为视网膜色素上皮和内皮细胞之间参与维持视网膜内稳态的关键相互依赖相互作用提供了证据。