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Modulation of CD4 antigen on macrophages and microglia in rat brain

Modulation of CD4 antigen on macrophages and microglia in rat brain
Modulation of CD4 antigen on macrophages and microglia in rat brain
Mononuclear phagocytes which express the HIV entry receptor CD4 have been implicated as possible sites of virus replication in brain, but there is still considerable uncertainty as to which cells in the CNS express CD4 Ag. Although it is not susceptible to HIV infection the rat provides a model to define expression of the CD4 Ag on MO in brain. We report that the CD4 epitopes W3/25 and OX35 are found only on monocytes, MO, microglia, and occasional lymphocytes and not on neurons, other glia, or endothelium. CD4 Ag levels are modulated during microglial differentiation, after reactivation after local inflammation, and within the intact blood brain barrier. MO and microglia also express other potential plasma membrane binding and entry sites for HIV viz Fc and complement receptors that are regulated independently of CD4.
0022-1007
1138-1143
Perry, V.H.
8f29d36a-8e1f-4082-8700-09483bbaeae4
Gordon, S.
df664ae8-6319-4b1a-8f16-49f4a5fe760f
Perry, V.H.
8f29d36a-8e1f-4082-8700-09483bbaeae4
Gordon, S.
df664ae8-6319-4b1a-8f16-49f4a5fe760f

Perry, V.H. and Gordon, S. (1987) Modulation of CD4 antigen on macrophages and microglia in rat brain. Journal of Experimental Medicine, 166 (4), 1138-1143. (doi:10.1084/jem.166.4.1138).

Record type: Article

Abstract

Mononuclear phagocytes which express the HIV entry receptor CD4 have been implicated as possible sites of virus replication in brain, but there is still considerable uncertainty as to which cells in the CNS express CD4 Ag. Although it is not susceptible to HIV infection the rat provides a model to define expression of the CD4 Ag on MO in brain. We report that the CD4 epitopes W3/25 and OX35 are found only on monocytes, MO, microglia, and occasional lymphocytes and not on neurons, other glia, or endothelium. CD4 Ag levels are modulated during microglial differentiation, after reactivation after local inflammation, and within the intact blood brain barrier. MO and microglia also express other potential plasma membrane binding and entry sites for HIV viz Fc and complement receptors that are regulated independently of CD4.

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Published date: 1 October 1987

Identifiers

Local EPrints ID: 491777
URI: http://eprints.soton.ac.uk/id/eprint/491777
ISSN: 0022-1007
PURE UUID: 506c83e8-e549-4b58-bdf0-de6311eb10bf

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Date deposited: 03 Jul 2024 17:30
Last modified: 10 Jul 2024 21:43

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Contributors

Author: V.H. Perry
Author: S. Gordon

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