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The recovery of the B-cell population in adult thymectomized lethally irradiated and bone marrow-reconstituted mice.

机译:成年经胸腺切除致死性照射和骨髓重建的小鼠中B细胞种群的恢复。

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摘要

The recovery of the B-cell population in adult thymectomized, irradiated and bone marrow-reconstituted mice (T X BM mice was estimated at various times after bone marrow transplantation. The spleen cells to be tested were mixed with dexamethasone-resistant thymocytes (DRT) and sheep red blood cells (SRBC) and transferrred to irradiated recipients. The number of plaque-forming cells (PFC) in the spleen of the recipients was determined 7 days later. Using this functional B-cell assay a sequential appearance of the precursors of IgM-, IgG- and IgA-PFC in the spleen of T X BM mice was observed. The precursors of IgM-PFG (IgM-B cells) were present immediately after transplantation. The first IgG-B cells could be detected at 13-16 days after transplantation and the IgA-B cells finally appeared at 22 days after transplantation. The number of B cells reached a constant and normal level at 30 days after transplantation. The IgM-, IgG- and IgA-B cell development in sham-thymectomized, irradiated and bone narrow-reconstituted mice (ST X BM mice) was virtually the same as in T X BM mice.
机译:成年的经胸腺切除,放射和骨髓重建的小鼠(TX BM小鼠在骨髓移植后的不同时间)的B细胞群的恢复。将要测试的脾细胞与耐地塞米松的胸腺细胞(DRT)混合,绵羊红细胞(SRBC)并转移到受辐照的接受者。7天后确定接受者脾脏中斑块形成细胞(PFC)的数量。使用这种功能性B细胞测定法连续检测IgM前体在TX BM小鼠的脾脏中观察到了-,IgG-和IgA-PFC,移植后立即出现了IgM-PFG的前体(IgM-B细胞),在第13-16天就可以检测到第一个IgG-B细胞。移植后第22天,IgA-B细胞终于出现;移植后30天,B细胞的数量达到恒定和正常水平。假手术切除的IgM-,IgG-和IgA-B细胞的发育,辐照的骨骼狭窄重建小鼠(ST X BM小鼠)与T X BM小鼠基本相同。

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