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单克隆抗λ5抗体FS1可识别一种与早期前B细胞系表面的λ5和Vpre-B相关的130 kDa蛋白。

Monoclonal anti-lambda 5 antibody FS1 identifies a 130 kDa protein associated with lambda 5 and Vpre-B on the surface of early pre-B cell lines.

作者信息

Shinjo F, Hardy R R, Jongstra J

机构信息

Toronto Hospital Research Institute, Ontario, Canada.

出版信息

Int Immunol. 1994 Mar;6(3):393-9. doi: 10.1093/intimm/6.3.393.

DOI:10.1093/intimm/6.3.393
PMID:8186191
Abstract

mAbs specific for mouse lambda 5 protein were prepared by fusion of spleen cells from a hamster immunized with recombinant lambda 5 protein synthesized in bacteria and the mouse myeloma cell line SP2/0-Ag14. Here we report the characteristics of the antibodies produced by the FS1 hybridoma. FS1 antibody stains a variety of mouse pre-B cell lines but not B cell lines or T cell lines. The staining of the pre-B cell lines A-1 and C-7 by phycoerythrin (PE)-conjugated FS1 (FS1-PE) can be blocked by preincubation of these cells with unconjugated FS1 antibody or with affinity purified polyclonal lambda 5 specific Ig but not with normal hamster or mouse IgG or with affinity purified polyclonal anti-Mb-1 Ig. From these experiments we concluded that FS1 specifically recognizes lambda 5 protein. We used FS1-PE to probe for surface (s) lambda 5+ cells in normal BALB/c mouse bone marrow. Such cells were undetectable when total bone marrow or FACS sorted subpopulations were analyzed. However, when B220+, CD43+, s lambda 5-bone marrow cells were cultured for 4 days on the stromal cell line FLST2 in the presence of IL-7, s lambda 5 expression became apparent. Further expansion of these cells in IL7 alone augmented the s lambda 5 expression to readily detectable levels. This modulation may indicate that s lambda 5 expression on normal bone marrow cells in vivo is transient and that at any given moment only a small fraction of bone marrow cells expresses low levels of lambda 5 protein on the surface.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

用在细菌中合成的重组λ5蛋白免疫的仓鼠的脾细胞与小鼠骨髓瘤细胞系SP2/0-Ag14融合,制备了针对小鼠λ5蛋白的单克隆抗体。在此,我们报告了FS1杂交瘤产生的抗体的特性。FS1抗体可对多种小鼠前B细胞系进行染色,但对B细胞系或T细胞系无染色作用。用藻红蛋白(PE)偶联的FS1(FS1-PE)对前B细胞系A-1和C-7进行染色时,可通过将这些细胞与未偶联的FS1抗体或亲和纯化的多克隆λ5特异性Ig预先孵育来阻断,但不能用正常仓鼠或小鼠IgG或亲和纯化的多克隆抗-Mb-1 Ig阻断。从这些实验中我们得出结论,FS1特异性识别λ5蛋白。我们用FS1-PE探测正常BALB/c小鼠骨髓中表面(s)λ5+细胞。当分析全骨髓或通过荧光激活细胞分选(FACS)分选的亚群时,未检测到此类细胞。然而,当B220+、CD43+、sλ5-骨髓细胞在白细胞介素-7(IL-7)存在的情况下在基质细胞系FLST2上培养4天时,sλ5表达变得明显。仅在IL-7中进一步扩增这些细胞可使sλ5表达增加到易于检测的水平。这种调节可能表明体内正常骨髓细胞上的sλ5表达是短暂的,并且在任何给定时刻只有一小部分骨髓细胞在表面表达低水平的λ5蛋白。(摘要截短于250字)

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1
Monoclonal anti-lambda 5 antibody FS1 identifies a 130 kDa protein associated with lambda 5 and Vpre-B on the surface of early pre-B cell lines.单克隆抗λ5抗体FS1可识别一种与早期前B细胞系表面的λ5和Vpre-B相关的130 kDa蛋白。
Int Immunol. 1994 Mar;6(3):393-9. doi: 10.1093/intimm/6.3.393.
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A complex of glycoproteins is associated with VpreB/lambda 5 surrogate light chain on the surface of mu heavy chain-negative early precursor B cell lines.一种糖蛋白复合物与μ重链阴性早期前体B细胞系表面的VpreB/λ5替代轻链相关联。
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The immunoglobulin light chain related protein lambda 5 is expressed on the surface of mouse pre-B cell lines and can function as a signal transducing molecule.免疫球蛋白轻链相关蛋白λ5在小鼠前B细胞系表面表达,并可作为信号转导分子发挥作用。
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The expression of the mouse VpreB/lambda 5 locus in transformed cell lines and tumors of the B lineage differentiation pathway.小鼠VpreB/λ5基因座在B细胞系分化途径的转化细胞系和肿瘤中的表达。
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引用本文的文献

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J Immunol. 2009 Jan 1;182(1):138-47. doi: 10.4049/jimmunol.182.1.138.
2
Loss of precursor B cell expansion but not allelic exclusion in VpreB1/VpreB2 double-deficient mice.VpreB1/VpreB2双缺陷小鼠中前体B细胞扩增丧失,但等位基因排斥未受影响。
J Exp Med. 2001 Feb 19;193(4):435-45. doi: 10.1084/jem.193.4.435.
3
Review article: role of the surrogate light chain and the pre-B-cell receptor in mouse B-cell development.
综述文章:替代轻链和前B细胞受体在小鼠B细胞发育中的作用
Immunology. 2000 Dec;101(4):435-41. doi: 10.1046/j.1365-2567.2000.00151.x.
4
A novel anti-Vpre-B antibody identifies immunoglobulin-surrogate receptors on the surface of human pro-B cells.一种新型抗Vpre-B抗体可识别人类前B细胞表面的免疫球蛋白替代受体。
J Exp Med. 1996 Jun 1;183(6):2693-8. doi: 10.1084/jem.183.6.2693.
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Fate of surrogate light chains in B lineage cells.B淋巴细胞系中替代轻链的命运
J Exp Med. 1996 Feb 1;183(2):421-9. doi: 10.1084/jem.183.2.421.