Cholesterol and oxysterols in retinal neuron-glia interactions: relevance for glaucoma

Elodie A.Y. Masson, Jeanne Serrano, Elise Léger-Charnay, Niyazi Acar
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Abstract

Cholesterol is an essential component of cellular membranes, crucial for maintaining their structural and functional integrity. It is especially important for nervous tissues, including the retina, which rely on high amounts of plasma membranes for the transmission of the nervous signal. While cholesterol is by far the most abundant sterol, the retina also contains cholesterol precursors and metabolites, especially oxysterols, which are bioactive molecules. Cholesterol lack or excess is deleterious and some oxysterols are known for their effect on neuron survival. Cholesterol homeostasis must therefore be maintained. Retinal glial cells, especially Müller cells, the principal glial cells of the vertebrate retina, provide mechanical, nutritional, and metabolic support for the neighboring neurons. Several pieces of evidence indicate that Müller cells are major actors of cholesterol homeostasis in the retina, as it is known for other glial cells in the brain. This process is based on a close cooperation with neurons, and sterols can be signaling molecules participating in glia-neuron interactions. While some implication of cholesterol in age-related macular degeneration is now recognized, based on epidemiological and laboratory data, evidence for its role in glaucoma is still scarce. The association between cholesterolemia and glaucoma is controversial, but experimental data suggest that sterols could take part in the pathological processes. It has been demonstrated that Müller glial cells are implicated in the development of glaucoma through an ambivalent reactive retinal gliosis process. The early steps contribute to maintaining retinal homeostasis and favor the survival of ganglion cells, which are targeted during glaucoma. If gliosis persists, dysregulation of the neuroprotective functions, cytotoxic effects of gliotic Müller cells and disruption of glia-neuron interactions lead to an acceleration of ganglion cell death. Sterols could play a role in the glial cell response to glaucomatous injury. This represents an understudied but attractive topic to better understand glaucoma and conceive novel preventive or curative strategies. The present review describes the current knowledge on i) sterol metabolism in retinal glial cells, ii) the potential role of cholesterol in glaucoma, and iii) the possible relationships between cholesterol and oxysterols, glial cells and glaucoma. Focus is put on glia-neuron interactions.
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视网膜神经元-胶质细胞相互作用中的胆固醇和氧甾醇:与青光眼的关系
胆固醇是细胞膜的重要组成部分,对维持细胞膜的结构和功能完整性至关重要。它对包括视网膜在内的神经组织尤为重要,因为神经信号的传递需要大量的质膜。虽然胆固醇是迄今为止含量最高的固醇,但视网膜中还含有胆固醇前体和代谢产物,尤其是生物活性分子氧基甾醇。胆固醇缺乏或过量都会造成危害,某些氧基甾醇对神经元的存活有影响。因此,必须维持胆固醇的平衡。视网膜胶质细胞,尤其是脊椎动物视网膜的主要胶质细胞--Müller 细胞,为邻近的神经元提供机械、营养和代谢支持。多项证据表明,Müller 细胞是视网膜胆固醇平衡的主要参与者,这与大脑中的其他神经胶质细胞一样。这一过程建立在与神经元密切合作的基础上,固醇可能是参与神经胶质细胞-神经元相互作用的信号分子。根据流行病学和实验室数据,胆固醇对老年性黄斑变性的影响现已得到认可,但胆固醇在青光眼中的作用的证据仍然很少。胆固醇血症与青光眼之间的关系尚存争议,但实验数据表明,固醇可能参与了病理过程。有研究表明,Müller 神经胶质细胞与青光眼的发病有关,是通过一个矛盾的反应性视网膜胶质增生过程发生的。早期步骤有助于维持视网膜的平衡,有利于神经节细胞的存活,而神经节细胞是青光眼的目标。如果神经胶质增生持续存在,神经保护功能失调、神经胶质 Müller 细胞的细胞毒性作用以及神经胶质-神经元相互作用的破坏将导致神经节细胞加速死亡。甾醇可能在神经胶质细胞对青光眼损伤的反应中发挥作用。这是一个研究不足但却很有吸引力的课题,有助于更好地了解青光眼,并构想新的预防或治疗策略。本综述介绍了有关以下方面的现有知识:i) 视网膜胶质细胞中的固醇代谢;ii) 胆固醇在青光眼中的潜在作用;iii) 胆固醇和氧固醇、胶质细胞和青光眼之间的可能关系。重点是神经胶质细胞与神经元之间的相互作用。
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