β-2微球蛋白
淀粉样变性
腕管综合征
淀粉样蛋白(真菌学)
血液透析
医学
纤维
氨基酸
淀粉样纤维
生物化学
化学
病理
内科学
外科
淀粉样β
疾病
作者
Fumitake Gejyo,Shoji Okada,Toshiyuki Yamada,Noriyuki Honma,Hidehiko Saito,Yasushi Suzuki,Yoichi Nakagawa,Hiroyuki Kobayashi,Yoshihiro Maruyama,Yoshihei Hirasawa,Masashi Suzuki,Masaaki Arakawa
摘要
Carpal tunnel syndrome (CTS) has been associated with amyloid deposits and is now regarded as a major complication in chronic hemodialysis patients. While this new syndrome has been receiving increasing attention, its etiology has not been clarified. We have isolated amyloid fibrils from amyloid laden tissues inside the carpal tunnel in four different hemodialysis patients with CTS. After solubilization in guanidine HCl, a significant amount of the protein was located in a homogeneous, low molecular weight fraction. Each protein was found to be identical to beta 2-microglobulin with regard to its molecular weight of 11,000 on SDS-PAGE, amino acid composition and N-terminal amino acids: Ile-Gln-Arg-Thr-Pro-Lys-Ile-Gln-Val-Tyr-Ser-Arg-His-Pro-Ala-Glu. In direct immunofluorescent study, anti-beta 2-microglobulin did react positively with amyloid deposits. These results demonstrate that the amyloid associated with chronic hemodialysis contains as major component a new form of amyloid fibril protein that is homologous to beta 2-microglobulin. It is postulated that beta 2-microglobulin cannot be removed from the blood by conventional hemodialysis, and accumulates in tissues causing the formation of amyloid fibrils, which, having a relatively high affinity to the carpal tunnel area, thus causes CTS.
科研通智能强力驱动
Strongly Powered by AbleSci AI