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Current Aging Science • December 2012<br />

Aluminum excytotoxicity and neuroautotoimmunity:<br />

the role of the brain expression of<br />

CD32+ (FcyRIIa), ICAM-1+ and CD3E in aging<br />

Author information<br />

Jovanova-Nesic K1, Shoenfeld Y, Spector NH.<br />

Immunology Research Center Branislav Jankovic<br />

Department of Neuroimmunology, Institute of Virology<br />

Vaccines and Sera-Torlak, Belgrade, Serbia<br />

Abstract<br />

In the central nervous system (CNS) microglia are crucial for the defense of the brain<br />

against invading microorganisms, formation of tumors, and damage following trauma.<br />

However, uncontrolled activation of these cells may have deleterious outcomes<br />

through activation of Fcy and the complement 3 receptors and the induction of an<br />

adaptive immune reaction. Proteins contributing to this reaction are the intercellular<br />

adhesion molecule-1 (ICAM-1) and CD3 molecules, among others. Both can be expressed<br />

on the glia cells before cytokine release and may facilitate an autoimmune<br />

inflammatory reaction in the brain. Round microglial cells among the pyramidal<br />

cells of the hippocampus with increased expression of CD32+ (FcyIIa) and near the<br />

site of injection of aluminum were detected immunohistochemically and indicate<br />

microglial activation at the site of aluminum injury. ICAM-1+ immunoreactivity<br />

significantly increased in the hippocampus and in the choroids plexus, indicating<br />

increased inflammation in the brain as well as increased CD3E+ expression in the<br />

hippocampus and non-MHC-restricted T cytotoxicity after aluminum injection. The<br />

pattern of expression of CD32+ (FcyIIa receptor) near the site of aluminum injection<br />

indicates that microglia may play a phagocytic role at the site of aluminum-induced<br />

excitotoxicity in the brain. Significant expression of ICAM-1+ and CD3E+<br />

immunoreactive cells with the clusters of ICAM-1+ in the choroid plexus suggests<br />

a consequently neurotoxic autoimmune reaction induced by microglial hyperactivation<br />

in the injured brain.<br />

“In the central nervous system (CNS)<br />

microglia are crucial for the defense of the brain<br />

against invading microorganisms, formation of tumors,<br />

and damage following trauma. However, uncontrolled<br />

activation of these cells may have deleterious outcomes ...”<br />

http://www.ncbi.nlm.nih.gov/pubmed/23387884

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