A Further Analysis and Commentary on: Profiling Changes in Cortical Astroglial Cells Following Chronic Stress

Gianfilippo Coppola, G. Rurak, Stephanie Simard, N. Salmaso
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引用次数: 4

Abstract

The neuroplasticity hypothesis of depression proposes that major depressive disorders are related to decreased hippocampal and cortical neural plasticity, which is reversed by antidepressant treatment. Astroglial cells have emerged as key mediators of neural plasticity and are involved in the cause and treatment of depression and anxiety-like behaviors. One of the ways that astroglia modulate neuroplasticity is through the formation and maintenance of perineuronal nets (PNNs). Perineuronal nets are important extracellular matrix components that respond to stress and are implicated in anxiety-like behaviors. Normally, astroglial cells continuously turnover PNNs by degrading and donating PNN proteins; however, chronic stress slows PNN protein degradation and increases cortical PNN expression overall. In this report, we used weighted gene co-expression network analysis and eigengene analysis to further delineate the pathways and key regulators involved in the astroglial-PNN relationship following chronic stress. Our analyses indicate that chronic variable stress induces the expression of PNNs through inhibition of trophic pathways and key transcription factors in astroglial cells. These data further support the integral role of astroglial cells in the neuroplasticity hypothesis of depression through their modulation of anxiety-like behaviors and PNNs.
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对慢性应激后皮质星形胶质细胞图谱变化的进一步分析和评述
抑郁症的神经可塑性假说认为,重度抑郁症与海马和皮层神经可塑性降低有关,而抗抑郁药物治疗可逆转这种可塑性。星形胶质细胞已成为神经可塑性的关键介质,并参与抑郁和焦虑样行为的病因和治疗。星形胶质细胞调节神经可塑性的途径之一是通过形成和维持神经周围网络(pnn)。神经周围网络是重要的细胞外基质成分,对压力作出反应,并涉及焦虑样行为。正常情况下,星形胶质细胞通过降解和供体PNN蛋白不断地更新PNN;然而,慢性应激减缓了PNN蛋白的降解,并增加了皮层PNN的表达。在本报告中,我们使用加权基因共表达网络分析和特征基因分析来进一步描绘慢性应激后星形胶质细胞- pnn关系的途径和关键调节因子。我们的分析表明,慢性可变应激通过抑制星形胶质细胞的营养通路和关键转录因子来诱导PNNs的表达。这些数据进一步支持星形胶质细胞通过调节焦虑样行为和pnn在抑郁症的神经可塑性假说中的整体作用。
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