Astrocyte and Macrophage Regulation of YKL-40 Expression and Cellular Response in Neuroinflammation

被引:144
作者
Bonneh-Barkay, Dafna [1 ]
Bissel, Stephanie J. [1 ]
Kofler, Julia [1 ]
Starkey, Adam [1 ]
Wang, Guoji [1 ]
Wiley, Clayton A. [1 ]
机构
[1] Univ Pittsburgh, Dept Pathol, Pittsburgh, PA USA
关键词
astrocytes; macrophages; neuroinflammation; YKL-40; HUMAN CARTILAGE GLYCOPROTEIN; CHITINASE-LIKE PROTEIN; GROWTH-FACTOR-BETA; SERUM YKL-40; ALTERNATIVE ACTIVATION; CELLS; INHIBITION; MONOCYTE; CHI3L1; FAMILY;
D O I
10.1111/j.1750-3639.2011.00550.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Numerous inflammatory conditions are associated with elevated YKL-40 expression by infiltrating macrophages. Thus, we were surprised to observe minimal macrophage and abundant astrocyte expression of YKL-40 in neuroinflammatory conditions. The aims of the current study were to better delineate this discrepancy, characterize the factors that regulate YKL-40 expression in macrophages and astrocytes and study whether YKL-40 expression correlates with cell morphology and/or activation state. In vitro, macrophages expressed high levels of YKL-40 that was induced by classical activation and inhibited by alternative activation. Cytokines released from macrophages induced YKL-40 transcription in astrocytes that was accompanied by morphological changes and altered astrocytic motility. Because coculturing of astrocytes and macrophages did not reverse this in vitro expression pattern, additional components of the in vivo central nervous system (CNS) milieu must be required to suppress macrophage and induce astrocyte expression of YKL-40.
引用
收藏
页码:530 / 546
页数:17
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