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
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.