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Astrocyte Atrophy and Immune Dysfunction in Self-Harming Macaques
Author(s) -
Kim M. Lee,
Kevin B. Chiu,
Hope A. Sansing,
Fiona M. Inglis,
Kate C. Baker,
Andrew G. MacLean
Publication year - 2013
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0069980
Subject(s) - astrocyte , glial fibrillary acidic protein , biology , immune system , atrophy , neuroscience , astrogliosis , gliosis , white matter , pathology , immunology , immunohistochemistry , medicine , central nervous system , magnetic resonance imaging , radiology
Background Self-injurious behavior (SIB) is a complex condition that exhibits a spectrum of abnormal neuropsychological and locomotor behaviors. Mechanisms for neuropathogenesis could include irregular immune activation, host soluble factors, and astrocyte dysfunction. Methods We examined the role of astrocytes as modulators of immune function in macaques with SIB. We measured changes in astrocyte morphology and function. Paraffin sections of frontal cortices from rhesus macaques identified with SIB were stained for glial fibrillary acidic protein (GFAP) and Toll-like receptor 2 (TLR2). Morphologic features of astrocytes were determined using computer-assisted camera lucida. Results There was atrophy of white matter astrocyte cell bodies, decreased arbor length in both white and gray matter astrocytes, and decreased bifurcations and tips on astrocytes in animals with SIB. This was combined with a five-fold increase in the proportion of astrocytes immunopositive for TLR2. Conclusions These results provide direct evidence that SIB induces immune activation of astrocytes concomitant with quantifiably different morphology.

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