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淋巴细胞的IgD受体。

IgD receptors of lymphoid cells.

作者信息

Pernis B, Forni L

出版信息

Immunol Commun. 1976;5(9):807-26. doi: 10.3109/08820137609047621.

Abstract

While present in normal human serum in very low amounts and undetectable in sera of non-human primates as well as of mice, IgD is found on the surface of the majority of B lymphocytes in all the above mentioned species. Lymphocytes which carry IgD on their membrane also have IgM. The two molecules are present in relative amounts that can be very different in different cells. Both IgM and IgD of a single cell are the actual product of the cell itself. They have the same light chain and, more importantly, the same combining site and idiotype. IgD/IgM bearing lymphocytes are the majority of all B lymphocytes in spleen, lymph nodes and Peyer's patches, whereas in bone marrow they account for half of the immunoglobulin positive cells. Although the percentage of double IgD/IgM cells is very similar in different tissues, the total amount of IgD, as well as the relative amounts of IgD and IgM as detected by biochemical methods varies. In fact, lymph nodes, and even more Peyer's patches are much richer than spleen in cells having levels of IgD higher than those of IgM; conversely, in the bone marrow, all the positive cells have very low levels of IgD. In ontogeny, as in evolution, IgD appears after IgM: in human foetuses IgD bearing cells are not detectable before 13 weeks of gestation, and in the mouse they appear only after birth. IgD receptors seem to disappear from B cells which undergo maturation to secretion, as indicated by the fact that only a proportion of IgM secreting plasma cells show membrane IgD. IgD is never found on the membrane of IgG-containing cells, and also lymphocytes bearing simultaneously IgD and IgG are very rare, and it might well be that for these cells, the double expression for short periods of time does not actually correspond to simultaneous synthesis.

摘要

IgD在正常人血清中的含量极低,在非人类灵长类动物以及小鼠的血清中无法检测到,但在上述所有物种的大多数B淋巴细胞表面都能发现它。细胞膜上携带IgD的淋巴细胞也有IgM。这两种分子的相对含量在不同细胞中可能有很大差异。单个细胞的IgM和IgD都是该细胞自身的实际产物。它们具有相同的轻链,更重要的是,具有相同的结合位点和独特型。带有IgD/IgM的淋巴细胞在脾脏、淋巴结和派伊尔结中占所有B淋巴细胞的大多数,而在骨髓中它们占免疫球蛋白阳性细胞的一半。尽管双IgD/IgM细胞在不同组织中的百分比非常相似,但通过生化方法检测到的IgD总量以及IgD和IgM的相对含量有所不同。事实上,淋巴结,尤其是派伊尔结中,IgD水平高于IgM的细胞比脾脏丰富得多;相反,在骨髓中,所有阳性细胞的IgD水平都非常低。在个体发育过程中,如同在进化过程中一样,IgD在IgM之后出现:在人类胎儿中,妊娠13周前无法检测到携带IgD的细胞,在小鼠中它们仅在出生后出现。IgD受体似乎在经历成熟至分泌的B细胞中消失,这一事实表明,只有一部分分泌IgM的浆细胞显示膜IgD。在含IgG的细胞表面从未发现IgD,同时携带IgD和IgG的淋巴细胞也非常罕见,很可能对于这些细胞来说,短时间的双重表达实际上并不对应于同时合成。

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