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通过在Fv - 2位点同基因的小鼠品系之间制备的同种抗血清检测到的晚期红细胞祖细胞上的新型分化抗原。

Novel differentiation antigens on late erythrocytic progenitor cells detected by alloantisera made between mouse strains congenic at the Fv-2 locus.

作者信息

Vaithilingam D S, Axelrad A A

出版信息

J Exp Med. 1982 May 1;155(5):1491-500. doi: 10.1084/jem.155.5.1491.

Abstract

We have investigated the activities of alloantisera produced in B6 (C57BL/6) and B6.S strain mice reciprocally immunized with unwashed bone marrow and spleen cell suspensions from their respective Fv-2 congenic partner strains, B6.S and B6. These antisera inhibited the formation of colonies by the late erythrocytic progenitors (CFU-E) in plasma cultures seeded with unwashed bone marrow or spleen cells; washed cells were unaffected. Erythropoietic burst formation by the early progenitors (BFU-E) was not significantly inhibited by the antisera, whether the cells were washed or unwashed. We conclude (a) that the congenic antisera are capable of recognizing alloantigens controlled by alleles of Fv-2 or of a closely linked gene locus on chromosome 9; (b) that these alloantigens are situated on the surface of erythrocytic progenitor cells and can be removed by washing; and (c) that the expression of the alloantigens on these cells is influenced by their stage of differentiation.

摘要

我们研究了在B6(C57BL/6)和B6.S品系小鼠中产生的同种抗血清的活性,这些小鼠分别用来自其各自Fv-2同源近交系伙伴品系B6.S和B6的未洗涤骨髓和脾细胞悬液进行相互免疫。这些抗血清抑制了用未洗涤骨髓或脾细胞接种的血浆培养物中晚期红细胞祖细胞(CFU-E)形成集落;洗涤后的细胞不受影响。无论细胞是否洗涤,早期祖细胞(BFU-E)形成红细胞生成爆发均未被抗血清显著抑制。我们得出以下结论:(a)同源抗血清能够识别由Fv-2等位基因或9号染色体上紧密连锁的基因座控制的同种抗原;(b)这些同种抗原位于红细胞祖细胞表面,可通过洗涤去除;(c)这些细胞上同种抗原的表达受其分化阶段的影响。

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