Department of Ophthalmology, Schepens Eye Research Institute of Massachusetts Eye and Ear, Harvard Medical School, Boston, MA, 02114, USA.
Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA, 02115, USA.
Mol Neurodegener. 2023 Sep 27;18(1):68. doi: 10.1186/s13024-023-00658-9.
The optic nerve is an important tissue in glaucoma and the unmyelinated nerve head region remains an important site of many early neurodegenerative changes. In both humans and mice, astrocytes constitute the major glial cell type in the region, and in glaucoma they become reactive, influencing the optic nerve head (ONH) microenvironment and disease outcome. Despite recognizing their importance in the progression of the disease, the reactive response of optic nerve head astrocytes remains poorly understood.
To determine the global reactive response of ONH astrocytes in glaucoma we studied their transcriptional response to an elevation in IOP induced by the microbead occlusion model. To specifically isolate astrocyte mRNA in vivo from complex tissues, we used the ribotag method to genetically tag ribosomes in astrocytes, restricting analysis to astrocytes and enabling purification of astrocyte-associated mRNA throughout the entire cell, including the fine processes, for bulk RNA-sequencing. We also assessed the response of astrocytes in the more distal myelinated optic nerve proper (ONP) as glaucomatous changes manifest differently between the two regions.
Astrocytes of the optic nerve exhibited a region-specific and temporally distinct response. Surprisingly, ONH astrocytes showed very few early transcriptional changes and ONP astrocytes demonstrated substantially larger changes over the course of the experimental period. Energy metabolism, particularly oxidative phosphorylation and mitochondrial protein translation emerged as highly upregulated processes in both ONH and ONP astrocytes, with the former showing additional upregulation in antioxidative capacity and proteolysis. Interestingly, optic nerve astrocytes demonstrated a limited neuroinflammatory response, even when challenged with a more severe elevation in IOP. Lastly, there were a greater number of downregulated processes in both astrocyte populations compared to upregulated processes.
Our findings demonstrate an essential role for energy metabolism in the response of optic nerve astrocytes to elevated IOP, and contrary to expectations, neuroinflammation had a limited overall role. The transcriptional response profile is supportive of the notion that optic nerve astrocytes have a beneficial role in glaucoma. These previously uncharacterized transcriptional response of optic nerve astrocytes to injury reveal their functional diversity and a greater heterogeneity than previously appreciated.
视神经是青光眼的重要组织,未髓鞘化的神经头区域仍然是许多早期神经退行性变化的重要部位。在人类和小鼠中,星形胶质细胞构成该区域的主要神经胶质细胞类型,在青光眼患者中,它们会发生反应,影响视神经头(ONH)微环境和疾病结果。尽管认识到它们在疾病进展中的重要性,但视神经头星形胶质细胞的反应性仍知之甚少。
为了确定青光眼患者视神经头星形胶质细胞的整体反应,我们研究了它们对微珠阻塞模型引起的眼压升高的转录反应。为了在体内从复杂组织中特异性分离视神经头星形胶质细胞的 mRNA,我们使用核糖体标签方法在星形胶质细胞中遗传标记核糖体,将分析限制在星形胶质细胞内,并能够对整个细胞包括精细过程中的星形胶质细胞相关 mRNA 进行纯化,用于批量 RNA-seq。我们还评估了在更远端有髓鞘的视神经本身(ONP)中星形胶质细胞的反应,因为这两个区域的青光眼变化表现不同。
视神经中的星形胶质细胞表现出区域特异性和时间上的不同反应。令人惊讶的是,ONH 星形胶质细胞表现出很少的早期转录变化,而 ONP 星形胶质细胞在实验过程中表现出更大的变化。能量代谢,特别是氧化磷酸化和线粒体蛋白翻译,在 ONH 和 ONP 星形胶质细胞中均被高度上调,前者在抗氧化能力和蛋白水解方面表现出额外的上调。有趣的是,即使面对更高的眼压升高,视神经星形胶质细胞的神经炎症反应也很有限。最后,与上调过程相比,两种星形胶质细胞群体中下调过程的数量更多。
我们的研究结果表明,能量代谢在视神经头星形胶质细胞对眼压升高的反应中起着至关重要的作用,与预期相反,神经炎症的总体作用有限。转录反应谱支持这样一种观点,即视神经头星形胶质细胞在青光眼中有有益的作用。这些以前未被描述的视神经头星形胶质细胞对损伤的转录反应揭示了它们的功能多样性和比以前所认识到的更大的异质性。