Figure 1
Figure 1. Reduced frequencies of ETP in the steady thymus of CCR7−/−CCR9−/− mice. Thymocytes from wild-type (wt), CCR7−/−, CCR9−/−, and CCR7−/−CCR9−/− (DKO) mice were stained with antibodies against lineage markers, CD4, CD8, CD25, CD44, and CD117 and analyzed by flow cytometry. (A) Analysis of early T-lineage progenitor (ETP; Lin−CD25−CD44+CD117hi). (B) Analysis of DN2 (Lin−CD25+CD44+CD117+) and DN3 (Lin−CD25+CD44−CD117−/lo) compartments. (C) Analysis of double-negative (DN), double-positive (DP), and single-positive (SP) populations. Numbers in quadrants and adjacent to gates represent frequencies of viable thymocytes. (D) Statistical analysis of flow cytometric results from multiple individual mice (wt: n = 36, CCR7−/−: n = 8, CCR9−/−: n = 3, DKO: n = 12). Data represent mean ± SEM.

Reduced frequencies of ETP in the steady thymus of CCR7−/−CCR9−/− mice. Thymocytes from wild-type (wt), CCR7−/−, CCR9−/−, and CCR7−/−CCR9−/− (DKO) mice were stained with antibodies against lineage markers, CD4, CD8, CD25, CD44, and CD117 and analyzed by flow cytometry. (A) Analysis of early T-lineage progenitor (ETP; LinCD25CD44+CD117hi). (B) Analysis of DN2 (LinCD25+CD44+CD117+) and DN3 (LinCD25+CD44CD117−/lo) compartments. (C) Analysis of double-negative (DN), double-positive (DP), and single-positive (SP) populations. Numbers in quadrants and adjacent to gates represent frequencies of viable thymocytes. (D) Statistical analysis of flow cytometric results from multiple individual mice (wt: n = 36, CCR7−/−: n = 8, CCR9−/−: n = 3, DKO: n = 12). Data represent mean ± SEM.

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