Holmes F E, Haynes L W
School of Biological Sciences, University of Bristol, UK.
Neurosci Lett. 1996 Aug 9;213(3):185-8. doi: 10.1016/0304-3940(96)12855-x.
We have investigated the activity of the Ca(2+)-dependent apoptosis-related transglutaminase type 2 in the mnd/mnd mouse mutant. Transglutaminase activity in mnd/mnd central nervous system (CNS) tissue homogenates was identical to that of healthy animals at 3 months of age, but at 8 months it was greater in the mnd/mnd CNS by up to four times, depending on the region. Western blot analysis showed no difference in the level of immunoreactive transglutaminase type 2 in spinal cord homogenates between mnd/mnd and healthy mice. However, a greater number of acyl donor protein substrates of transglutaminase were identified in mnd/mnd tissue. N epsilon (gamma-Glutamyl)lysine cross-linked product of transglutaminase activity was localized to the soma of degenerating motor neurons in the mnd/mnd mouse spinal cord. We conclude that neurodegeneration in the mnd/mnd mouse is accompanied by activation of transglutaminase at substrate level. Possible mechanisms of activation and its implications for cellular pathology are discussed.
我们研究了钙依赖性凋亡相关转谷氨酰胺酶2型在运动神经元病(mnd)/mnd小鼠突变体中的活性。mnd/mnd中枢神经系统(CNS)组织匀浆中的转谷氨酰胺酶活性在3月龄时与健康动物相同,但在8月龄时,根据区域不同,mnd/mnd中枢神经系统中的活性比健康动物高多达四倍。蛋白质免疫印迹分析表明,mnd/mnd小鼠和健康小鼠脊髓匀浆中免疫反应性转谷氨酰胺酶2型的水平没有差异。然而,在mnd/mnd组织中鉴定出了更多的转谷氨酰胺酶酰基供体蛋白底物。转谷氨酰胺酶活性的Nε(γ-谷氨酰基)赖氨酸交联产物定位于mnd/mnd小鼠脊髓中退化运动神经元的胞体。我们得出结论,mnd/mnd小鼠的神经退行性变伴随着转谷氨酰胺酶在底物水平的激活。本文讨论了激活的可能机制及其对细胞病理学的影响。