Mehr R, Perelson A S, Fridkis-Hareli M, Globerson A
Theoretical Division, Los Alamos National Laboratory, NM 87545, USA.
J Theor Biol. 1996 Jul 21;181(2):157-67. doi: 10.1006/jtbi.1996.0122.
Recent findings suggest that mature T cells in the thymus may regulate the growth and differentiation of immature thymocytes. Here we use mathematical modeling and computer simulations to identify the thymocyte subsets that might serve as targets for regulation, and the processes that might be affected by regulation. Our results suggest that thymocyte development is subject to regulation through two feedback loops: mature CD4+ T cells exert a positive feedback on the single positive CD4+8- thymocyte compartment, by reducing CD4+8- cell death and possibly accelerating the differentiation of CD4+8+ thymocytes into CD4+8- thymocytes; they may also exert a negative feedback on the double-positive CD4+8+ thymocyte compartment, by reducing the proliferation or accelerating the maturation of these cells.
最近的研究结果表明,胸腺中的成熟T细胞可能调节未成熟胸腺细胞的生长和分化。在此,我们使用数学建模和计算机模拟来确定可能作为调节靶点的胸腺细胞亚群,以及可能受调节影响的过程。我们的结果表明,胸腺细胞发育受到两个反馈回路的调节:成熟的CD4⁺ T细胞对单阳性CD4⁺8⁻胸腺细胞区室施加正反馈,通过减少CD4⁺8⁻细胞死亡并可能加速CD4⁺8⁺胸腺细胞向CD4⁺8⁻胸腺细胞的分化;它们也可能对双阳性CD4⁺8⁺胸腺细胞区室施加负反馈,通过减少这些细胞的增殖或加速其成熟。