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抗原引发的B淋巴细胞分化。IV. 来自致敏和未致敏小鼠的抗体形成细胞祖细胞的黏附特性。

Antigen-initiated B lymphocyte differentiation. IV. The adherence properties of antibody-forming cell progenitors from primed and unprimed mice.

作者信息

Schlegel R A, Shortman K

出版信息

J Immunol. 1975 Jul;115(1):94-9.

PMID:1097508
Abstract

Distinct sub-populations of B lymphocytes may be fractionated by passage through glass-bead columns, due to a temperature-independent adherence of certain cells. The relative adherence properties of AFC-progenitors from spleens of primed or unprimed CBA mice were compared with an adoptive immune assay employing as antigen the hapten NIP on the carrier polymerized flagellin, under conditions where T lymphocytes did not limit the response. The AFC-progenitors for an anti-NIP IgM response from unprimed mice, whether conventional, germ-free, or athymic were more adherent than the majority of cells in the spleen. The AFC-progenitors for an IgG response from hapten-primed mice were less adherent that the majority of spleen cells. The results indicate that there are sub-classes of AFC-progenitors, differing in surface properties and probably corresponding to differences between the "antigen-inexperienced" and the "memory" B cell populations.

摘要

由于某些细胞具有不依赖温度的黏附性,通过玻璃珠柱可以分离出不同的B淋巴细胞亚群。在T淋巴细胞不限制反应的条件下,采用载体聚合鞭毛蛋白上的半抗原NIP作为抗原的过继免疫测定法,比较了初免或未初免CBA小鼠脾脏中抗半抗原抗体产生细胞(AFC)祖细胞的相对黏附特性。未初免小鼠中产生抗NIP IgM反应的AFC祖细胞,无论是常规小鼠、无菌小鼠还是无胸腺小鼠的,都比脾脏中的大多数细胞更具黏附性。初免小鼠中产生IgG反应的AFC祖细胞比大多数脾细胞的黏附性低。结果表明,存在AFC祖细胞亚类,其表面特性不同,可能对应于“无抗原经验”和“记忆”B细胞群体之间的差异。

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引用本文的文献

1
Heterogeneity of murine B-lymphocytes.小鼠B淋巴细胞的异质性。
Indian J Pediatr. 1982 May-Jun;49(398):415-22. doi: 10.1007/BF02834437.
2
Antigen-initiated B-lymphocyte differentiation. VII. Quantification of AFC progenitor levels in adoptive and culture responses to NIP-POL antigen.抗原引发的B淋巴细胞分化。VII. 对NIP-POL抗原的过继性和培养反应中AFC祖细胞水平的定量分析。
Immunology. 1975 Dec;29(6):1029-40.
3
Optimal strategies in immunology. II. B memory cell production.免疫学中的优化策略。II. B记忆细胞的产生。
J Math Biol. 1978 Mar 28;5(3):213-56. doi: 10.1007/BF00276120.
4
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J Exp Med. 1976 May 1;143(5):1220-38. doi: 10.1084/jem.143.5.1220.