Development of the thymus requires signaling through the fibroblast growth factor receptor R2-IIIb

JM Revest, RK Suniara, K Kerr, JJT Owen… - The Journal of …, 2001 - journals.aai.org
JM Revest, RK Suniara, K Kerr, JJT Owen, C Dickson
The Journal of Immunology, 2001journals.aai.org
Mice deficient for fibroblast growth factor (Fgf) R2-IIIb show a block in thymic growth after
embryonic day 12.5, a stage that just precedes its detection in thymic epithelial cells. Fgf7
and Fgf10, the main ligands for FgfR2-IIIb, are expressed in the mesenchyme surrounding
the thymic epithelial primordium, and Fgf10-deficient mice also exhibit impaired thymic
growth. Hence, Fgf signaling is essential for thymic epithelial proliferation. In addition to the
proliferative block, most thymic epithelial cells fail to progress from an immature cytokeratin 5 …
Abstract
Mice deficient for fibroblast growth factor (Fgf) R2-IIIb show a block in thymic growth after embryonic day 12.5, a stage that just precedes its detection in thymic epithelial cells. Fgf7 and Fgf10, the main ligands for FgfR2-IIIb, are expressed in the mesenchyme surrounding the thymic epithelial primordium, and Fgf10-deficient mice also exhibit impaired thymic growth. Hence, Fgf signaling is essential for thymic epithelial proliferation. In addition to the proliferative block, most thymic epithelial cells fail to progress from an immature cytokeratin 5-positive to a cytokeratin 5-negative phenotype. Nevertheless, sufficient epithelial cell differentiation occurs in the severely hypoplastic thymus to allow the development of CD4/CD8-double-positive thymocytes and a very small number of single-positive thymocytes expressing TCRs.
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