Increased endothelial expression of transglutaminase in glioblastomas

被引:11
作者
Hilton, DA [1 ]
Love, S [1 ]
Barber, R [1 ]
机构
[1] Frenchay Hosp, Dept Neuropathol, Bristol BS16 1LE, Avon, England
关键词
glioma; transglutaminase; apoptosis; tumour vasculature;
D O I
10.1111/j.1365-2990.1997.tb01328.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Transglutaminases are a family of calcium-dependent enzymes that catalyse the formation of covalent crosslinks between proteins. They have several diverse functions and are thought to be involved in cell differentiation, apoptosis and blood coagulation. We have investigated the expression of tissue transglutaminase in five fibrillary astrocytomas, five anaplastic astrocytomas and seven glioblastomas by immunohistochemistry. Strongly labelled tumour cells were seen in most of the fibrillary and anaplastic astrocytomas and all of the glioblastomas. Labelling was particularly prominent in the pseudopalisading tumour cells that surrounded foci of necrosis and apoptosis in glioblastomas. Most of the immunostained cells did not themselves show morphological features of apoptosis. In addition, apoptotic cells were demonstrated using in situ end-labelling and by in situ hybridization with digoxigenin-labelled poly(A) oligonucleotide probes. Apoptotic cells demonstrated by both of these methods were most numerous in anaplastic astrocytomas and glioblastomas, However, their distribution did not correlate with that of the tumour cells showing transglutaminase labelling. Strong transglutaminase labelling was also observed in the endothelial cells of vessels showing microvascular proliferation in all of the glioblastomas studied. In contrast, endothelial transglutaminase labelling was weak or absent in lower grade astrocytic tumours. Enhanced expression of transglutaminase by endothelial cells in glioblastomas may contribute to the high prevalence of vascular thrombosis and necrosis in these tumours.
引用
收藏
页码:507 / 511
页数:5
相关论文
共 19 条
[1]   APOPTOTIC HEPATOCYTES BECOME INSOLUBLE IN DETERGENTS AND CHAOTROPIC AGENTS AS A RESULT OF TRANSGLUTAMINASE ACTION [J].
FESUS, L ;
THOMAZY, V ;
AUTUORI, F ;
CERU, MP ;
TARCSA, E ;
PIACENTINI, M .
FEBS LETTERS, 1989, 245 (1-2) :150-154
[2]  
Folk J E, 1977, Adv Protein Chem, V31, P1, DOI 10.1016/S0065-3233(08)60217-X
[3]   IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION [J].
GAVRIELI, Y ;
SHERMAN, Y ;
BENSASSON, SA .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :493-501
[4]  
GREENBERG CS, 1987, BLOOD, V70, P702
[5]   TRANSGLUTAMINASES - MULTIFUNCTIONAL CROSS-LINKING ENZYMES THAT STABILIZE TISSUES [J].
GREENBERG, CS ;
BIRCKBICHLER, PJ ;
RICE, RH .
FASEB JOURNAL, 1991, 5 (15) :3071-3077
[6]   EXPRESSION OF THE CYTOSOLIC AND PARTICULATE FORMS OF TRANSGLUTAMINASE DURING CHEMICALLY-INDUCED RAT-LIVER CARCINOGENESIS [J].
HAND, D ;
ELLIOTT, BM ;
GRIFFIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 970 (02) :137-145
[7]  
HILTON DA, 1997, J HISTOCHEM CYTOCHEM, V45, P1
[8]  
IWAKI T, 1994, AM J PATHOL, V145, P776
[9]  
JOHNSON TS, 1994, ONCOGENE, V9, P2935
[10]  
Kleihues P., 1993, HISTOLOGICAL TYPING