Up-regulation of VCAM1 Relates to Neuronal Apoptosis After Intracerebral Hemorrhage in Adult Rats

• DOI: 10.1007/s11064-015-1561-x
• Publication Date: 2015-04-13T18:24:27Z
• Authors: Dongmei Zhang; Damin Yuan; Jianhong Shen; Yaohua Yan; Chen Gong; Jun Gu; Huaqing Xue; Yuhang Qian; Weidong Zhang; Xiaojuan He; Li Yao; Yuhong Ji; Aiguo Shen
• Keywords: Male; Neurons; 0301 basic medicine; Age Factors; Vascular Cell Adhesion Molecule-1; Apoptosis; PC12 Cells; Rats; Up-Regulation; 3. Good health; Rats, Sprague-Dawley; 03 medical and health sciences; Animals; Cerebral Hemorrhage

Vascular cell adhesion molecule 1 (VCAM1) is a member of the Immunoglobulin superfamily and encodes a cell surface sialoglycoprotein expressed in cytokine-activated endothelium. This type I membrane protein mediates leukocyte-endothelial cell adhesion, facilitates the downstream signaling, and may play a role in the development of artherosclerosis and rheumatoid arthritis. Accumulating evidence has demonstrated that VCAM1 exerts an anti-apoptotic effect in several tumor tissues such as ovarian cancer and breast cancer. Intracerebral hemorrhage (ICH) is the second most common subtype of stroke with high morbidity and mortality, which imposes a big burden on individuals and the whole society. These together prompted us to question whether VCAM1 has some association with neuron apoptosis during the pathological process of ICH. An ICH rat model was established and assessed by behavioral tests in order to explore the role of VCAM1 after ICH. Up-regulation of VCAM1 was observed in brain areas surrounding the hematoma following ICH by western blotting and immunohistochemistry. Immunofluorescence manifested VCAM1 was strikingly increased in neurons, but not in astrocytes and microglia. Furthermore, we detected that neuronal apoptosis marker active caspase-3 had co-localizations with VCAM1. At the same time, Bcl-2 was also co-localized with VCAM1. Taken together, our findings suggested that VCAM1 might be involved in the neuronal apoptosis and pathophysiology of ICH.