Intercellular Protein Transfer from Thymocytes to Thymic Epithelial Cells.
Abstract
Promiscuous expression of tissue restricted antigens (TRAs) in medullary thymic epithelial
cells (mTECs) is crucial for negative selection of self-reactive T cells to establish
central tolerance. Intercellular transfer of self-peptide-MHC complexes from mTECs
to thymic dendritic cells (DCs) allows DCs to acquire TRAs, which in turn contributes
to negative selection and regulatory T cell generation. However, mTECs are unlikely
to express all TRAs, such as immunoglobulins generated only in B cells after somatic
recombination, hyper-mutation, or class-switches. We report here that both mTECs and
cortical TECs can efficiently acquire not only cell surface but also intracellular
proteins from thymocytes. This reveals a previously unappreciated intercellular sharing
of molecules from thymocytes to TECs, which may broaden the TRA inventory in mTECs
for establishing a full spectrum of central tolerance.
Type
Journal articleSubject
AnimalsEpithelial Cells
Extracellular Space
Hematopoiesis
Luminescent Proteins
Major Histocompatibility Complex
Mice, Inbred C57BL
Proteins
Receptors, Antigen, T-Cell
Thymocytes
Thymus Gland
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https://hdl.handle.net/10161/11812Published Version (Please cite this version)
10.1371/journal.pone.0152641Publication Info
Wang, Hong-Xia; Qiu, Yu-Rong; & Zhong, Xiao-Ping (2016). Intercellular Protein Transfer from Thymocytes to Thymic Epithelial Cells. PLoS One, 11(3). pp. e0152641. 10.1371/journal.pone.0152641. Retrieved from https://hdl.handle.net/10161/11812.This is constructed from limited available data and may be imprecise. To cite this
article, please review & use the official citation provided by the journal.
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Show full item recordScholars@Duke
Xiaoping Zhong
Professor of Pediatrics
The immune system protects the host from microbial infection but can cause diseases
if not properly controlled. My lab is interested in the receptor signaling mediated
regulation of immune cell development and function as well as the pathogenesis and
treatment of autoimmune diseases and allergies. We are currently investigating the
roles diacylglycerol kinases (DGKs) and TSC1/2-mTOR play in the immune system. DGKs
are a family of ten enzymes that catalyze the conversion of diacylgl

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