Granzyme-b mediated cell death in the spinal cord-injured rat model.

Authors: Chaitanya, GV  Kolli, M  Babu, PP 
Citation: Chaitanya GV, etal., Neuropathology. 2008 Dec 24.
Pubmed: (View Article at PubMed) PMID:19170890
DOI: Full-text: DOI:10.1111/j.1440-1789.2008.00980.x

Spinal cord injury initiates a complex series of inflammatory and immune responses including the influx of monocytes, macrophages, T-cells, NK cells and so on, into the injured area. In the present study, we found a significant increase in the levels of granzyme-b (gra-b) from the first day after the transection until the third day, with decrease in intensity thereafter. The chemokine IP-10/CXCL10 was also found to be elevated along with gra-b correlating with the infiltration of CD-8(+) cytotoxic T lymphocytes (CTLs) into the injured spinal cord. We observed an increase in the levels of the 64 kDa poly ADP ribose polymerase fragment, known to be a signature fragment produced by gra-b. Localization of gra-b in TUNEL positive neurons indicates that gra-b might play a crucial role in neuronal death and contributes to the pathophysiology of spinal cord injury.

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RGD Object Information
RGD ID: 2311365
Created: 2009-07-08
Species: All Species
Last Modified: 2009-07-08
Status: ACTIVE