Study of the intracellular trafficking of the pre-T-cell receptor and its role in T-cell lineage commitment

T-cell development is a complex multi-step process, driving the maturation of hematopoietic stem cells into fully functional mature T-cells that play a major role in the adaptive immune response against pathogens. This developmental process is regulated by a series of checkpoints in which the signalling capacity of the T-cell antigen receptor (TCR) is tested. One such checkpoint is the generation of the clonotypic chains of the two TCR variants (αβ-TCR or γδ-TCR) by V(D)J recombination. Importantly, the TCRα chain is rearranged only after correct TCRβ expression, which requires the latter chain to pair with a surrogate invariant pre-Tα chain to form the pre-TCR complex. While both TCR variants activate the same signalling pathway, they commit the T cells to distinct functional lineages. Insight into how thymocytes are nonetheless able to distinguish between these two signals is crucial to our fundamental understanding of T-cell development and how it might be manipulated therapeutically. Pertinently, the pre-TCR is undetectable at the cell surface, unlike the γδ TCR which is primarily located at the plasma membrane. In this thesis, I aim to investigate whether the distinct intracellular localisation of the pre-TCR provides a mean for this signal to be distinguished from that of the γδ-TCR. Through the reconstitution of pre-TCR expression in a non-immune cell, I show that although the pre-TCR can in fact translocate to the cell surface, it is rapidly removed via clathrin-mediated endocytosis and transported to lysosomes. The use of a non-immune cell permits the study of pre-TCR trafficking in the absence of other signalling components and demonstrates that this intracellular localisation of the pre-TCR is intrinsic to the receptor. Using a panel of truncated and engineered pre-TCR, I demonstrate that the absence of a second Ig domain in the extracellular domain of the pre-Tα chain promotes the rapid endocytosis of the receptor. In a thymocyte-OP9-DL1 co-culture system, I show that recombination-deficient thymocytes expressing a pre-TCR variant lacking the TCRβ variable domain is sufficient to drive cells through the TCRβ-selection checkpoint and give rise to double positive cells. Likewise, wild type thymocytes over-expressing the pre-TCR or a receptor with a fused TCRα variable domain may push thymocytes down the γδ-lineage. Finally, I employ a biotin proximity-labelling assay to screen for binding partners of the pre-TCR that might mediate its internalisation. Using this method, I identify TMEM131, a novel protein with an unknown function and characterise some of its biochemical and cell biological properties.

Name dc:type.qualificationname

Doctor of Philosophy (PhD)

Level dc:type.qualificationlevel

Doctoral

Grantor dc:publisher.institution

University of Cambridge

Year dc:date.issued

2019

Author dc:creator

• Smid, Andrei Iosif

Advisor dc:contributor.advisor

• James, John Robert

• T-cell
• T-cell development
• Pre-T-cell receptor
• Trafficking
• TCR signalling
• γδ-TCR
• OP9-DL1 co-culture
• hematopoietic stem cells
• BioID2

Licence

• https://apollo8-f-pro.lib.cam.ac.uk/bitstreams/1556d7c0-8e21-4cb7-95b3-2efe8f7a3fe6/download
• https://www.rioxx.net/licenses/all-rights-reserved/

Language dc:language

en

Author Identifier

0000-0001-9732-0059
0000-0003-1452-7578

OAI identifier oai:identifier

oai:www.repository.cam.ac.uk:1810/297674