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PMID: 9500964 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Astrocytes regulate microglial phagocytosis of senile plaque cores of Alzheimer's disease.

Experimental neurology ·Vol. 149 ·No. 2 ·1998-02-00 ·Pages 329-40

DeWitt DA, Perry G, Cohen M, Doller C, Silver J

Abstract

We have developed an in vitro model in which isolated senile plaque (SP) cores are presented to rat microglial cells in culture. Microglia rapidly phagocytosed, broke apart, and cleared SP cores. However, when cocultured with astrocytes, microglial phagocytosis was markedly suppressed, allowing the SPs to persist. Suppression of phagocytosis by astrocytes appears to be a general phenomena since microglia in the presence of astrocytes showed reduced capacity to phagocytose latex beads as well. The astrocyte effect on microglia is related in part to a diffusible factor(s) since astrocyte- but not fibroblast-conditioned media also reduced phagocytosis. These results suggest that while microglia have the capacity to phagocytose and remove SPs, astrocytes which lie in close association to microglia may help prevent the efficient clearance of SP material allowing them to persist in Alzheimer's disease.

MeSH Terms
Alzheimer Disease/pathology,physiopathology Animals Animals, Newborn Astrocytes/cytology,physiology,ultrastructure Brain/pathology Cells, Cultured Cerebral Cortex/cytology,physiology Coculture Techniques Frontal Lobe/pathology Humans Microglia/cytology,physiology Phagocytosis Plaque, Amyloid/pathology,ultrastructure Rats Rats, Sprague-Dawley Temporal Lobe/pathology
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
DeWitt D A
Department of Neurosciences, Case Western Reserve University, Cleveland, Ohio 44106, USA.
Perry G
Cohen M
Doller C
Silver J
Article Info
Journal
Experimental neurology
Abbr.
Exp Neurol
ISSN
0014-4886
Published
1998-02-00
Pages
329-40
Language
English
Region
United States
NLM ID
0370712
Subset
IM
Grants
NIA NIH HHS · AG-00105-11A1 · United States
NIA NIH HHS · AG09287 · United States
NINDS NIH HHS · NS25713 · United States
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