BST-1, A SURFACE-MOLECULE OF BONE-MARROW STROMAL CELL-LINES THAT FACILITATES PRE-B-CELL GROWTH

被引:170
作者
KAISHO, T
ISHIKAWA, J
ORITANI, K
INAZAWA, J
TOMIZAWA, H
MURAOKA, O
OCHI, T
HIRANO, T
机构
[1] OSAKA UNIV,SCH MED,DEPT ENVIRONM MED,SUITA,OSAKA 565,JAPAN
[2] KYOTO PREFECTURAL UNIV MED,DEPT HYG,KYOTO 602,JAPAN
关键词
CD38; RHEUMATOID ARTHRITIS;
D O I
10.1073/pnas.91.12.5325
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Bone marrow stromal cells are essential for B-lymphocyte development. However, how stromal cells regulate B lymphopoiesis is not clear. In this paper, we report the molecular cloning of a stromal cell line-derived glycosylphosphatidylinositol-anchored molecule, BST-1, that facilitates pre-B-cell growth. The deduced amino acid sequence of BST-1 exhibited 33% identity with CD38. BST-1 was expressed in a wide range of tissues and in umbilical vein endothelial cells, whereas it was scarcely expressed in a variety of hematopoietic cell lines. The gene for BST-1 was assigned to chromosome 14q32.3, where immunoglobulin heavy-chain genes are clustered. BST-1 expression was enhanced in rheumatoid arthritis patient-derived bone marrow stromal cell lines that were previously shown to have an enhanced ability to support the growth of a pre-B-cell line as compared with stromal cell lines derived from healthy donors.
引用
收藏
页码:5325 / 5329
页数:5
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