Reactive morphology of dividing microglia following kainic acid administration.

Reactive morphology of dividing microglia following kainic acid administration.
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DOI:
10.3389/fnins.2022.972138
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发表时间:
2022
影响因子:
4.3
通讯作者:
Rowe, Rachel K.
Rowe, Rachel K.
中科院分区:
医学2区
文献类型:
--
作者:
Green, Tabitha R. F.;Murphy, Sean M.;Moreno-Montano, Maria P.;Audinat, Etienne;Rowe, Rachel K.

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The microglial response to a pathological microenvironment is hallmarked by a change in cellular morphology. Following a pathological stimulus, microglia become reactive and simultaneously divide to create daughter cells. Although a wide array of microglial morphologies has been observed, the exact functions of these distinct morphologies are unknown, as are the morphology and reactivity status of dividing microglia. In this study, we used kainic acid to trigger microglial activation and cell division. Following a cortical kainic acid injection, microglial morphology and proliferation were examined at 3 days post-injection using immunohistochemistry for ionized calcium binding adapter molecule 1 (Iba1) to stain for microglia, and KI67 as a marker of cell division. Individual microglial cells were isolated from photomicrographs and skeletal and fractal analyses were used to examine cell size and spatial complexity. We examined the morphology of microglia in both wildtype and microglia-specific tumor necrosis factor (TNF)-α knockout mice. Data were analyzed using generalized linear mixed models or a two-way ANOVA. We found that dividing microglia had a more reactive morphology (larger cell body area, longer cell perimeter, and less ramification) compared to microglia that were not dividing, regardless of microglial release of TNF-α. However, we also observed dividing microglia with a complex, more ramified morphology. Changes in microglial morphology and division were greatest near the kainic acid injection site. This study uses robust and quantitative techniques to better understand microglial cell division, morphology, and population dynamics, which are essential for the development of novel therapeutics that target microglia.
耦合的增殖和凋亡维持成人大脑中小胶质细胞的快速离职。
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