Neuronal Morphology Networks and Systems Biology Laboratory, Division of Human Anatomy, Department of Mental and Physical Health and Preventive Medicine, University of Campania Luigi Vanvitelli, 80138 Naples, Italy.
Department of Neuroanatomy, Institute of Anatomy and Cell Biology, Faculty of Medicine, University of Freiburg, 79104 Freiburg, Germany.
Int J Mol Sci. 2024 Feb 16;25(4):2346. doi: 10.3390/ijms25042346.
Microglia and astrocytes are essential in sustaining physiological networks in the central nervous system, with their ability to remodel the extracellular matrix, being pivotal for synapse plasticity. Recent findings have challenged the traditional view of homogenous glial populations in the brain, uncovering morphological, functional, and molecular heterogeneity among glial cells. This diversity has significant implications for both physiological and pathological brain states. In the present study, we mechanically induced a Schaffer collateral lesion (SCL) in mouse entorhino-hippocampal slice cultures to investigate glial behavior, i.e., microglia and astrocytes, under metalloproteinases (MMPs) modulation in the lesioned area, CA3, and the denervated region, CA1. We observed distinct response patterns in the microglia and astrocytes 3 days after the lesion. Notably, GFAP-expressing astrocytes showed no immediate changes post-SCL. Microglia responses varied depending on their anatomical location, underscoring the complexity of the hippocampal neuroglial network post-injury. The MMPs inhibitor GM6001 did not affect microglial reactions in CA3, while increasing the number of Iba1-expressing cells in CA1, leading to a withdrawal of their primary branches. These findings highlight the importance of understanding glial regionalization following neural injury and MMPs modulation and pave the way for further research into glia-targeted therapeutic strategies for neurodegenerative disorders.
小胶质细胞和星形胶质细胞对于维持中枢神经系统的生理网络至关重要,其重塑细胞外基质的能力对于突触可塑性至关重要。最近的发现挑战了大脑中同质神经胶质群体的传统观点,揭示了神经胶质细胞之间在形态、功能和分子水平上的异质性。这种多样性对生理和病理脑状态都有重要意义。在本研究中,我们通过机械诱导小鼠齿状回-海马切片培养物中的 Schaffer 侧支损伤(SCL),来研究在 MMP 调节下损伤区域 CA3 和去神经区域 CA1 中胶质细胞(即小胶质细胞和星形胶质细胞)的行为。我们在损伤后 3 天观察到小胶质细胞和星形胶质细胞的明显反应模式。值得注意的是,GFAP 表达的星形胶质细胞在 SCL 后没有立即发生变化。小胶质细胞的反应因它们的解剖位置而异,强调了损伤后海马神经胶质网络的复杂性。MMP 抑制剂 GM6001 并没有影响 CA3 中的小胶质细胞反应,而增加了 CA1 中表达 Iba1 的细胞数量,导致它们的初级分支缩回。这些发现强调了理解神经损伤后神经胶质细胞分区和 MMP 调节的重要性,并为针对神经退行性疾病的神经胶质靶向治疗策略的进一步研究铺平了道路。