## Abstract In this review we summarize mechanisms of Ca^2+^ signaling in microglial cells and the impact of Ca^2+^ signaling and Ca^2+^ levels on microglial function. So far, Ca^2+^ signaling has been only characterized in cultured microglia and thus these data refer rather to activated microglia
Immunoregulation of microglial functional properties
✍ Scribed by Alison K. Cross; M. Nicola Woodroofe
- Publisher
- John Wiley and Sons
- Year
- 2001
- Tongue
- English
- Weight
- 217 KB
- Volume
- 54
- Category
- Article
- ISSN
- 1059-910X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Microglia are the resident tissue macrophages of the central nervous system (CNS) parenchyma and are key players in the initiation of an inflammatory response. Microglia rapidly transform from a resting to an activated morphology in response to a variety of disease states. However, they can also be the target of infections, as in the case of HIV. Many of the effector properties of microglia can be attributed to the array of substances they secrete in response to stimuli such as bacterial lipopolysaccharide, cytokines, and chemokines. The products of activated microglia include: cytokines (pro‐ and anti‐inflammatory), chemokines, nitric oxide, superoxide radicals, and proteases. Furthermore, microglia have the ability to present antigen to T cells, migrate in response to chemotactic stimuli, and phagocytose cell debris. This report focuses on the immunomodulatory functions of microglia, with particular attention to chemokines, and highlights their pivotal role in the CNS. Microsc. Res. Tech. 54:10–17, 2001. © 2001 Wiley‐Liss, Inc.
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