首页> 外文期刊>東京慈惠会医科大学雑誌 >全身性エリテマトーデス患者の末梢血リンパ球におけるテロメラーゼ活性およびテロメア長の解析
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全身性エリテマトーデス患者の末梢血リンパ球におけるテロメラーゼ活性およびテロメア長の解析

机译:系统性红斑狼疮患者外周血淋巴细胞端粒酶活性和端粒长度的分析

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摘要

テロメアは真核生物の染色体末端に存在する DNA蛋白質複合体であり,染色体の安定化には 必須の構造であると考えられている.ヒトのテ ロメアDNAはTTAGGGの繰り返し構造で,染 色体末端に位置している.%We investigated the clinical significance of telomerase activity and telomere length in peripheral blood T cells (CD3 + ) and B cells (CD19 + ) of patients with systemic lupus erythematosus (SLE). Telomerase activity was measured with the telomeric repeat amplification protocol assay, and telomere length was measure with flow-fluorescence in situ hybridization. Patients with SLE were classified into those with active SLE and inactive SLE according to the SLE disease activity index (SLEDAI). The T cell telomerase activity was significantly higher in patients with active or inactive SLE than in healthy subjects. However, the degree of telomerase activity was not correlated with the SLEDAI. In contrast. B cell telomerase activity was significantly higher in patients with active SLE than in healthy subjects and was strongly correlated with the SLEDAI. The T cell telomere length was significantly shorter in patients with SLE than in healthy subjects, whereas B cell telomere length did not differ between these two groups. These results suggest that in patients with SLE T cells are undergoing cell division continuously and that T cell telomerase activity is higher than normal but not high enough to prevent telomere shortening. However, we speculate that in B cells, cell division does not occur at an abnormally high rate in the inactive phase but occurs frequently in the active phase and that increased telomerase activity prevents telomere shortening.
机译:端粒是一种存在于真核染色体末端的DNA-蛋白质复合物,被认为是染色体稳定的必要结构。人端粒DNA是TTAGGG的重复结构,位于染料的末端。我们调查了系统性红斑狼疮(SLE)患者外周血T细胞(CD3 +)和B细胞(CD19 +)端粒酶活性和端粒长度的临床意义。根据SLE疾病活动指数(SLEDAI)将SLE患者分为活动性SLE和非活动性SLE患者,活动性或非活动性SLE患者的T细胞端粒酶活性明显更高相比之下,活动性SLE患者的B细胞端粒酶活性显着高于健康受试者,并且与SLEDAI密切相关.T。非活动性SLE较健康受试者更高,但是端粒酶活性的程度与SLEDAI无关。 SLE患者的细胞端粒长度明显短于健康受试者,而促进B细胞端粒长度却没有这些结果表明,在SLE患者中,T细胞正在连续分裂,并且T细胞端粒酶活性高于正​​常水平,但不足以防止端粒缩短。但是,我们推测在B细胞中,分裂在非活性期不会以异常高的速率发生,而是在活性期频繁发生,并且端粒酶活性的增加阻止了端粒的缩短。

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