Cutting edge: ectopic expression of the chemokine TCA4/SLC is sufficient to trigger lymphoid neogenesis

L Fan, CR Reilly, Y Luo, ME Dorf, D Lo - The Journal of Immunology, 2000 - journals.aai.org
L Fan, CR Reilly, Y Luo, ME Dorf, D Lo
The Journal of Immunology, 2000journals.aai.org
To test whether accumulation of naive lymphocytes is sufficient to trigger lymphoid
development, we generated mice with islet expression of the chemokine TCA4/SLC. This
chemokine is specific for naive lymphocytes and mature dendritic cells (DC) which express
the CCR7 receptor. Islets initially developed accumulations of T cells with DC, with scattered
B cells at the perimeter. These infiltrates consolidated into organized lymphoid tissue, with
high endothelial venules and stromal reticulum. Infiltrate lymphocytes showed a naive CD44 …
Abstract
To test whether accumulation of naive lymphocytes is sufficient to trigger lymphoid development, we generated mice with islet expression of the chemokine TCA4/SLC. This chemokine is specific for naive lymphocytes and mature dendritic cells (DC) which express the CCR7 receptor. Islets initially developed accumulations of T cells with DC, with scattered B cells at the perimeter. These infiltrates consolidated into organized lymphoid tissue, with high endothelial venules and stromal reticulum. Infiltrate lymphocytes showed a naive CD44 low CD25− CD69− phenotype, though half were CD62L negative. When backcrossed to RAG-1 knockout, DC were not recruited. Interestingly, islet lymphoid tissue developed in backcrosses to Ikaros knockout mice despite the absence of normal peripheral nodes. Our results indicate that TCA4/SLC can induce the development and organization of lymphoid tissue through diffential recruitment of T and B lymphocytes and secondary effects on stromal cell development.
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