Transglutaminase-catalyzed protein cross-linking in the molecular program of apoptosis and its relationship to neuronal processes

Authors
Citation
L. Fesus, Transglutaminase-catalyzed protein cross-linking in the molecular program of apoptosis and its relationship to neuronal processes, CELL MOL N, 18(6), 1998, pp. 683-694
Citations number
68
Categorie Soggetti
Neurosciences & Behavoir
Journal title
CELLULAR AND MOLECULAR NEUROBIOLOGY
ISSN journal
02724340 → ACNP
Volume
18
Issue
6
Year of publication
1998
Pages
683 - 694
Database
ISI
SICI code
0272-4340(199812)18:6<683:TPCITM>2.0.ZU;2-6
Abstract
1. One type of transglutaminase is usually accumulated in Various forms of naturally occurring cell death and apoptosis. The accumulated enzyme is act ivated during the death process, leading to the formation of cross-linked p rotein structures. Degradation of the cross-linked apoptotic bodies results in the elevation of the epsilon(gamma-glutamyl)lysine isodipeptide concent ration in body fluids, which may provide a diagnostic tool to monitor the a poptosis rate in various tissues under normal and pathologic conditions. 2. Extensive protein cross-linking may be directly related to the act of ki lling in some cells. In others, the effect of protein cross-linking is pall iative, preventing leakage of macromolecules and enhancing phagocytosis of the dead cells. 3. Tissue transglutaminase has been implicated in some physiologic function s of the nervous system. 4. The molecular machinery of apoptosis is present and easily evoked in neu ronal cells. 5. Effector elements of the apoptosis process have been associated with the pathogenesis of neurologic disorders. Tissue transglutaminase, representin g one of the effector elements of apoptosis, may be induced and activated i n cells following ischemia. It may also participate in the formation of abn ormal cell inclusions and A beta deposits in amyloid plaques.