Graduate Student UT Hlth. San Antonio San Antonio, Texas, United States
Introduction/Rationale: Cortical thymic epithelial cells (cTECs) establish a lymphopoietic thymocyte niche that regulates thymus size and T cell output throughout life. Our recent studies suggest that medullary TEC (mTEC)-derived fibroblast growth factor 21 (FGF21) acts in a paracrine manner to drive temporally distinct patterns of mTORC1 and mTORC2 signaling in cTECs. Thymic overexpression of FGF21 promoted thymus growth, enhanced T cell responsiveness to infection, and reduced indicators of age-associated autoimmunity. However, the cellular mechanisms regulating FGF21-dependent regulation of cTEC function across the lifespan have not been defined.
Methods: To determine whether cTEC-intrinsic FGF21–mTOR signaling regulates thymic architecture and function, we generated a new mouse model in which β5t-iCre drives cTEC-restricted deletion of the obligate FGF21 co-receptor, Klb, as well as expression of the Confetti multicolor reporter allele (β5t-iCre KlbF/F Confetti). We used flow cytometry and confocal microscopy to assess the kinetics of Klb expression, mTORC1/2 activity, thymic structure, cellular composition, T cell development, and cTEC morphology from birth to middle age in β5t-iCre KlbF/F Confetti mice and littermate controls.
Results: Together, our results suggest that cTECs directly respond to FGF21 signaling via the Klb receptor, and that mTORC1 and mTORC2 mediate cTEC-intrinsic FGF21 signaling to promote thymus size and function.
Conclusion: The conclusion is combined with the results.
