Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0168-0102(97)00033-3
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dc.titleInduction of major histocompatibility class II antigen on microglial cells in postnatal and adult rats following intraperitoneal injections of lipopolysaccharide
dc.contributor.authorNg, Y.-K.
dc.contributor.authorLing, E.-A.
dc.date.accessioned2015-09-09T07:03:29Z
dc.date.available2015-09-09T07:03:29Z
dc.date.issued1997-06
dc.identifier.citationNg, Y.-K., Ling, E.-A. (1997-06). Induction of major histocompatibility class II antigen on microglial cells in postnatal and adult rats following intraperitoneal injections of lipopolysaccharide. Neuroscience Research 28 (2) : 111-118. ScholarBank@NUS Repository. https://doi.org/10.1016/S0168-0102(97)00033-3
dc.identifier.issn01680102
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/120755
dc.description.abstractMicroglial cells, notably the ramified form, were induced to express major histocompability complex (MHC) class II antigen in postnatal and adult rats given intraperitoneal injections of lipopolysaccharide (LPS). The immunoreactive microglia which occurred in cell colonies or clusters were detected immunohistochemically with the monoclonal antibody OX-6. Some of the widely distributed MHC II positive cells were round or amoeboidic located preferentially in the perivascular area. In view of the widespread occurrence of microglial cells showing OX-6 immunoreactivity which is negligible in normal animals, it is suggested that the effect of LPS on microglia in vivo is a widespread phenomenon and is independent of age. It is suggested that the endotoxin not only triggers off the immunological potentiality of these cells but also elicits the entry of some mononuclear cells into the brain parenchyma.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S0168-0102(97)00033-3
dc.sourceScopus
dc.subjectBlood-brain barrier
dc.subjectLipopolysaccharide
dc.subjectMajor histocompability complex class II antigen
dc.subjectMicroglial cells
dc.typeArticle
dc.contributor.departmentANATOMY
dc.description.doi10.1016/S0168-0102(97)00033-3
dc.description.sourcetitleNeuroscience Research
dc.description.volume28
dc.description.issue2
dc.description.page111-118
dc.description.codenNERAD
dc.identifier.isiutA1997XJ02500003
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