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通过逆转录病毒介导的基因转移纠正 CD18 缺陷淋巴细胞。

Correction of CD18-deficient lymphocytes by retrovirus-mediated gene transfer.

作者信息

Wilson J M, Ping A J, Krauss J C, Mayo-Bond L, Rogers C E, Anderson D C, Todd R F

机构信息

Howard Hughes Medical Institute, Department of Internal Medicine, Ann Arbor, MI.

出版信息

Science. 1990 Jun 15;248(4961):1413-6. doi: 10.1126/science.1972597.

Abstract

Leukocyte adhesion deficiency (LAD) is an inherited disorder of leukocyte function caused by derangements in CD18 expression. The genetic and functional abnormalities in a lymphocyte cell line from a patient with LAD have been corrected by retrovirus-mediated transduction of a functional CD18 gene. Lymphocytes from patients with LAD were exposed to CD18-expressing retrovirus and enriched for cells that express CD11a and CD18 (LFA-1) on the cell surface. Molecular and functional analyses of these cells revealed (i) one copy of proviral sequence per cell, (ii) viral-directed CD18 RNA that exceeded normal endogenous levels, (iii) normal quantities of CD11a and CD18 protein on the cell surface, and (iv) reconstitution of LFA-1-dependent adhesive function.

摘要

白细胞黏附缺陷症(LAD)是一种由CD18表达紊乱引起的白细胞功能遗传性疾病。通过逆转录病毒介导的功能性CD18基因转导,已纠正了一名LAD患者淋巴细胞系中的遗传和功能异常。将LAD患者的淋巴细胞暴露于表达CD18的逆转录病毒中,并富集细胞表面表达CD11a和CD18(淋巴细胞功能相关抗原-1,LFA-1)的细胞。对这些细胞的分子和功能分析显示:(i)每个细胞有一份前病毒序列;(ii)病毒导向的CD18 RNA超过正常内源性水平;(iii)细胞表面CD11a和CD18蛋白数量正常;(iv)LFA-1依赖性黏附功能得以重建。

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