Babaya Naru, Ikegami Hiroshi, Fujisawa Tomomi, Nojima Koji, Itoi-Babaya Michiko, Inoue Kaori, Ohno Tamio, Shibata Masao, Ogihara Toshio
Department of Geriatric Medicine, Osaka University Graduate School of Medicine, Suita, Japan.
Biochem Biophys Res Commun. 2005 Mar 4;328(1):158-64. doi: 10.1016/j.bbrc.2004.12.149.
To study the contribution of beta-cell vulnerability to susceptibility to diabetes, we studied beta-cell vulnerability to a single high dose of streptozotocin (STZ) in an animal model of type 2 diabetes, the NSY mouse, a sister strain of the STZ-sensitive NOD mouse, in comparison with the STZ-resistant C3H mouse. NSY mice were found to be extremely sensitive to STZ. Introgression of a single Chr 11, where STZ-sensitivity was mapped in the NOD mouse, from NSY mice converted STZ-resistant C3H mice to STZ-sensitive. Two nucleotide substitutions were identified in the nucleoredoxin gene, a positional and functional candidate gene for STZ-induced diabetes on Chr 11. These data, together with the co-localization of type 1 (Idd4) and type 2 (Nidd1n) susceptibility genes on Chr 11, suggest that the intrinsic vulnerability of pancreatic beta cells is determined by a gene or genes on Chr 11, which may also contribute to susceptibility to spontaneous diabetes.
为了研究β细胞易损性对糖尿病易感性的影响,我们在2型糖尿病动物模型NSY小鼠(STZ敏感的NOD小鼠的姐妹品系)中,研究了β细胞对单次高剂量链脲佐菌素(STZ)的易损性,并与STZ抗性C3H小鼠进行比较。结果发现NSY小鼠对STZ极其敏感。将NSY小鼠中在NOD小鼠中定位到STZ敏感性的第11号染色体的一个片段导入STZ抗性C3H小鼠后,可使其转变为对STZ敏感。在第11号染色体上的核氧化还原蛋白基因中鉴定出两个核苷酸替换,该基因是STZ诱导糖尿病的定位和功能候选基因。这些数据,连同第11号染色体上1型(Idd4)和2型(Nidd1n)易感基因的共定位,表明胰腺β细胞的内在易损性由第11号染色体上的一个或多个基因决定,这也可能导致对自发性糖尿病的易感性。