Schuler W, Schuler A, Lennon G G, Bosma G C, Bosma M J
Fox Chase Cancer Center, Institute for Cancer Research, Philadelphia, PA 19111.
EMBO J. 1988 Jul;7(7):2019-24. doi: 10.1002/j.1460-2075.1988.tb03041.x.
The scid mouse mutant is severely deficient in lymphocytes; cells of the B or T lymphocyte lineage cannot be detected by either serological or functional assays. However, as shown here, germ-line transcripts of B cell immunoglobulin (Ig) constant and variable region genes and of T cell receptor (TCR) genes are detectable in lymphopoietic tissues of scid mice, as well as B and T lineage-specific lambda 5 and T3 delta transcripts. We conclude that B and T lineage-committed cells do arise in scid mice and that their Ig and TCR genes are accessible to enzymes involved in their recombination. This suggests that scid impairs lymphopoiesis at the stage at which antigen receptor genes normally undergo rearrangement.
严重联合免疫缺陷(scid)小鼠突变体的淋巴细胞严重缺乏;通过血清学或功能测定均无法检测到B或T淋巴细胞谱系的细胞。然而,如下所示,在scid小鼠的淋巴造血组织中可检测到B细胞免疫球蛋白(Ig)恒定区和可变区基因以及T细胞受体(TCR)基因的种系转录本,以及B和T谱系特异性的λ5和T3δ转录本。我们得出结论,scid小鼠中确实会出现B和T谱系定向细胞,并且它们的Ig和TCR基因可被参与其重组的酶作用。这表明scid在抗原受体基因正常进行重排的阶段损害了淋巴细胞生成。