Answers are grounded in this paper and cite their sources.
The expression of T cell-associated surface markers by lymphoid cells from congenitally athymic (nude) mice has been quantitatively investigated using flow microfluorometry. Spleen and lymph nodes from old (greater than 6 mo) nude mice on either a C57BL/6 or BALB/c genetic background were found to contain significant numbers (5 to 13% in spleen and 15 to 24% in lymph nodes) of cells expressing Thy-1 antigen. The proportion of Thy-1 positive cells in nude spleen was dramatically increased (to 22 to 67%) after passage of the cells over nylon wool columns. In contrast to older animals, young (1- to 2-mo-old) nude mice had undetectable levels (less than 1%) of Thy-1 bearing cells in spleen and reduced levels (6%) in lymph nodes. After passage of their spleen cells over nylon wool, some Thy-1 positive cells (10%) were detectable in 2-mo-old nude mice but none were detectable at 1 mo. In addition to Thy-1, we were able to detect the T cell alloantigens Lyt-1 and Lyt-2 on nylon wool-passed spleen cells from older C57BL/6 or BALB/c nu/nu mice. In general, the proportion of Lyt-1 bearing cells in nude lymphoid populations was similar to the proportion of Thy-1 positive cells. A smaller fraction of nude cells (corresponding to 35 to 59% of the total Thy-1 positive cells) were found to express Lyt-2. Analysis of the forward light scatter distributions of nude lymphoid cells bearing either Thy-1, Lyt-1, or Lyt-2 antigens further demonstrated that an overlapping population of relatively large-size cells expressed these surface markers. These data strongly imply that at least 2 subsets of T cells (i.e., Lyt-1+2- and Lyt-1+2+) develop in older nude mice in the apparent absence of thymic influence.
No takes yet. Share an insight, caveat, or question.
MacDonald et al. (1981) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: