Crinelli R, Bianchi M, Gentilini L, Magnani M, Hiscott J
Instuto di Chimica Biologica 'G. Fornaini', University of Urbino, Italy.
Eur J Biochem. 1999 Jul;263(1):202-11. doi: 10.1046/j.1432-1327.1999.00485.x.
Murine acquired immunodeficiency syndrome (MAIDS) is a complex immunopathology caused by a defective murine leukemia virus (LP-BM5) that mainly targets B-lymphocytes. Lymphadenophathy, splenomegaly, hypergammaglobulinemia and progressive immunodeficiency are prominent features of MAIDS. Previously, we showed that the ubiquitin proteolytic system was upregulated in infected lymph nodes [Crinelli, R., Fraternale, A., Casabianca, A. & Magnani, M. (1997) Eur. J. Biochem. 247, 91-97]. In this report, we demonstrate that increased 26S proteasome activity is responsible for accelerated turnover of the IkappaBalpha inhibitor in lymph node extracts derived from animals with MAIDS. The molecular mechanisms mediating IkappaBalpha proteolysis involved constitutive phosphorylation of IkappaBalpha at Ser32 and Ser36 and subsequent ubiquitination, suggesting persistent activation of an NF-kappaB inducing pathway. Interestingly, enhanced IkappaBalpha degradation did not result in enhanced NF-kappaB DNA binding activity, but rather in a different subunit composition. The modulation of NF-kappaB/IkappaB system may affect multiple immunoregulatory pathways and may in part explain the mechanisms leading to the profound immune dysregulation involved in MAIDS pathogenesis.
小鼠获得性免疫缺陷综合征(MAIDS)是一种由缺陷型小鼠白血病病毒(LP - BM5)引起的复杂免疫病理学疾病,该病毒主要靶向B淋巴细胞。淋巴结病、脾肿大、高球蛋白血症和进行性免疫缺陷是MAIDS的突出特征。此前,我们发现感染的淋巴结中泛素蛋白水解系统上调[Crinelli, R., Fraternale, A., Casabianca, A. & Magnani, M. (1997) Eur. J. Biochem. 247, 91 - 97]。在本报告中,我们证明26S蛋白酶体活性增加是导致MAIDS动物淋巴结提取物中IkappaBalpha抑制剂周转加速的原因。介导IkappaBalpha蛋白水解的分子机制涉及IkappaBalpha在Ser32和Ser36处的组成型磷酸化以及随后的泛素化,提示NF - kappaB诱导途径持续激活。有趣的是,IkappaBalpha降解增强并未导致NF - kappaB DNA结合活性增强,而是导致了不同的亚基组成。NF - kappaB/IkappaB系统的调节可能影响多种免疫调节途径,并且可能部分解释了导致MAIDS发病机制中严重免疫失调的机制。