Characterization of the common acute lymphoblastic leukaemia antigen (CD10) as an activation molecule on mature human B cells

Characterization of the common acute lymphoblastic leukaemia antigen (CD10) as an activation molecule on mature human B cells
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常见急性淋巴细胞白血病抗原 (CD10) 作为成熟人类 B 细胞激活分子的表征

DOI:
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发表时间:
1990
影响因子:
4.6
通讯作者:
J. Hata
J. Hata
中科院分区:
医学3区
文献类型:
--
作者:
N. Kiyokawa;Y. Kokai;K. Ishimoto;H. Fujita;J. Fujimoto;J. Hata

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使用体内和体外系统分析了B细胞活化期间CD 10分子的不同表达模式。通过双色流式细胞术分析,发现CD 10在体内活化B细胞的特定阶段表达。在B细胞活化过程中,CD 10的表达似乎与其他活化相关B细胞抗原(包括L29、MA 6、OKT 9和OKT 10)的表达不同。尽管CD 10的表达与活化相关的B细胞抗原的表达相关,但当通过细胞重力进行分级时,CD 10+ B细胞可以分离为与表达其他活化相关的B细胞抗原的细胞不同的部分。特别地,检测到某些CD 10 + B细胞对静息B细胞抗原L30呈阳性。体外研究表明,CD 10 + B细胞在B细胞活化的早期阶段由CD 10-B细胞产生,并且在被金黄色葡萄球菌科万I活化后消失。总之,CD 10是在B细胞活化过程的早期阶段瞬时表达的抗原。15例Burkitt淋巴瘤组织中CD 10及其它抗原的表达。所有病例均为CD 10+,87%(13例)同时为L 30+。此外,6例CD 10 + L30+病例为L29+。这一观察结果表明,伯基特淋巴瘤的表型相似的B细胞在活化的早期阶段,那些同时表达CD 10和L30。本研究已经解剖了一个精确的表达模式的CD 10成熟B细胞活化在体外和体内,并可能牵连的组织发生的一个不好的特点B细胞淋巴瘤,即伯基特淋巴瘤。
Distinct expression pattern of CD10 molecules during B cell activation was analysed using in vivo and in vitro systems. By two‐colour flowcytometrical analysis, CD10 was found to be expressed at a specificstage of in vivo activating B cells. The expression of CD10 during B cell activation appeared to be unique from that of other activation‐related B cell antigens including L29, MA6, OKT9 and OKT10. Although the expression of CD10 was associated with that of the activation‐related B cell antigens, CD 10+ B cells could be separated in the distinct fractions to those expressing other activation‐related B cell antigens when fractionated by cell gravity. In particular, certain CD10+ B cells were detected positive for the resting B cell antigen, L30. In vitro studies revealed that CD10+ B cells arose from CD10‐ B cells at an early step of B cell activation, and disappeared lately when activated by Staphylococcus aureus Cowan I. Collectively, CD10 was an antigen transiently expressed at an early phase of B cell activation process. Expression of CD10 and other antigens on Burkitt's lymphomas (15 cases) was studied next. All cases were CD10+, and 87% (13 cases) were also L30+. In addition, six of CD10+ L30+ cases were L29+. This observation suggested that Burkitt's lymphomas were phenotypically similar to the B cells at an early phase of activation, those expressing CD10 and L30, simultaneously. The present study has dissected a precise expression pattern of CD10 on mature B cell activation in vitro and in vivo, and could be implicated for the histogenesis of one of the poorly characterized B cell lymphoma, namely Burkitt's lymphoma.
DOI: 10.1182/blood.v70.5.1316.bloodjournal7051316
发表时间: 1987-11
期刊: Blood
影响因子: 20.3
作者:
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通讯作者: M. Loken;V. O. Shah;Karen L. Dattilio;C. Civin
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DOI: --
发表时间: 1986
期刊: Blood
影响因子: 20.3
作者:
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DOI: 10.1016/0090-1229(81)90193-8
发表时间: 1981
期刊: Clinical immunology and immunopathology
影响因子: --
作者:
Dagg,MK;Levitt,D
通讯作者: Levitt,D
从正常人骨髓中纯化常见急性淋巴细胞白血病抗原阳性细胞。
DOI: --
发表时间: 1984
期刊: Blood
影响因子: 20.3
作者:
Hokland,P;Nadler,LM;Griffin,JD;Schlossman,SF;Ritz,J
通讯作者: Ritz,J
B5,一种新的 B 细胞限制性激活抗原。
DOI: --
发表时间: 1985
期刊: Journal of immunology (Baltimore, Md. : 1950)
影响因子: --
作者:
Freedman,AS;Boyd,AW;Anderson,KC;Fisher,DC;Schlossman,SF;Nadler,LM
通讯作者: Nadler,LM