Mechanical actuators in microglia dynamics and function

被引:6
作者
Melo, Pedro [1 ]
Socodato, Renato [1 ]
Silveira, Mariana S. [1 ,2 ]
Neves, Miguel Antonio Dias [1 ]
Relvas, Joao Bettencourt [1 ]
Pinto, Ines Mendes [1 ,3 ]
机构
[1] Univ Porto, Inst Invest & Inovacao Saude i3S, Porto, Portugal
[2] Univ Fed Rio De Janeiro, Inst Biofis Carlos Chagas Filho, Rio De Janeiro, Brazil
[3] Int Iberian Nanotechnol Lab INL, Braga, Portugal
关键词
Non-muscle myosin II motors; Actin cytoskeleton dynamics; Cortical tension; Intracellular signal topography; Morphology; Microglial function; FIBRILLAR ALPHA-SYNUCLEIN; NONMUSCLE MYOSIN-II; MACROPHAGES; NANOTUBES; CONNECTIVITY; CONTRACTION; FORCE; CELLS;
D O I
10.1016/j.ejcb.2022.151247
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Microglia are the most prominent immune resident cell population in the central nervous system (CNS). In the healthy CNS, microglia survey their surrounding microenvironment, through recurrent extension and retraction of filopodia-like membrane protrusions, without evident cell body displacement. Microglia undergo dramatic transcriptomic and shape changes upon brain insults or neurodegenerative disease states and adopt a classical immune effector function (producing an extensive array of inflammatory mediators such as cytokines, chemokines, and reactive oxygen species) to re-establish tissue homeostasis. While the biophysical principles underlying microglia morphological changes remain elusive, several recent studies have highlighted the pivotal role of the actin and non-muscle myosin II filamentous cytoskeleton in this process. In this work, we discuss how subcellular topological patterning of the actin and myosin cytoskeleton can control microglial cell shape dynamics and how it can potentially feedback on their functional specialization, which is of great importance to understanding the mechanisms of microglial action in homeostatic conditions and CNS disease states.
引用
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页数:6
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