Szondy Z, Molnar P, Nemes Z, Boyiadzis M, Kedei N, Tóth R, Fésüs L
Department of Biochemistry, University School of Medicine, Debrecen, Hungary.
FEBS Lett. 1997 Mar 10;404(2-3):307-13. doi: 10.1016/s0014-5793(97)00140-3.
A significant increase in the expression and activity of tissue transglutaminase (tTG), one of the effector elements of apoptosis, was observed during involution of thymus elicited by treatment with either anti-CD3 antibody or dexamethasone or by irradiation. The blood plasma concentration of epsilon(gamma-glutamyl)lysine isodipeptide, the end-product of the digestion of transglutaminase cross-linked proteins, was also elevated in each of these cases. tTG was localized in cells of the cortical layer of the thymus and immunofluorescence double staining revealed that the enzyme appeared in the apoptotic cells. None of these observations could be made when apoptosis was induced by fas-receptor stimulation. The lack of tTG activity in fas-stimulated cells was accompanied with a less organized apoptotic morphology. Our data suggest that distinct signalling pathways, which induce apoptosis within the same cell type, can differentially regulate the expression of tTG, and this enzyme may be involved in structural stabilization of the apoptotic cells.
在通过抗CD3抗体或地塞米松治疗或照射引发的胸腺 involution 过程中,观察到组织转谷氨酰胺酶(tTG)(凋亡的效应元件之一)的表达和活性显著增加。在上述每种情况下,转谷氨酰胺酶交联蛋白消化的终产物ε(γ-谷氨酰基)赖氨酸异二肽的血浆浓度也升高。tTG定位于胸腺皮质层的细胞中,免疫荧光双重染色显示该酶出现在凋亡细胞中。当通过fas受体刺激诱导凋亡时,未观察到这些现象中的任何一种。fas刺激的细胞中tTG活性的缺乏伴随着凋亡形态的组织性较差。我们的数据表明,在同一细胞类型内诱导凋亡的不同信号通路可以差异调节tTG的表达,并且这种酶可能参与凋亡细胞的结构稳定。