SSA Stem cell regulation in the adult thymus

Lead Research Organisation: University of Edinburgh
Department Name: MRC Centre for Regenerative Medicine

Abstract

The thymus is a key organ of the adaptive immune system, responsible for T cell production throughout the lifespan. The organ has an intricate and highly organised architecture and cellularity, which is intimately linked to the different processes via which it produces a functional T cell repertoire. Of the different intrathymic cell-types, an array of specialized thymic epithelial cells (TEC) provides most of the functions required for T cell repertoire development. We are interested in developing stem cell-based approaches to boosting or replacing thymus function in patients. Through previous work, we identified the transcription factor, FOXN1, as a master regulator of TEC differentiation. Recently, we have shown that FOXN1 up-regulation can rejuvenate the thymus in aged animals (Bredenkamp Development 2014), and that expression of FOXN1 in a non-thymic cell-type, fibroblasts, forces these cells to change identity and become functional TEC (Bredenkamp Nature Cell Biology 2014). We call these reprogrammed cells induced TEC (iTEC). Additionally, we have identified a TEC stem cell population in the adult thymus (Ulyanchenko ...Blackburn, submitted). This project will further develop this work, by investigating how TEC stem cells are controlled in the adult organ and determining whether TEC stem cells can be generated by reprogramming. As part of this work, we will investigate transcription factor control of Foxn1 expression in TEC stem cells, and how self-renewal and differentiation of TEC stem cells is influenced by signals from other intrathymic cell types.
The project will utilise a range of state-of-the-art approaches to identify and validate transcriptional control networks in TEC stem cell, including genetic analyses (e.g. analysis of conditional knockouts, gene knock-down and over-expression approaches in vivo and in vitro), high resolution microscopy, multi-parameter flow cytometry, gene expression analysis (RNAseq and RT-qPCR). All of the required approaches are available within the Blackburn lab or within CRM. The student will also benefit from training and exchange opportunities available through the EU-funded consortium ThymiStem (www.thymistem.org).

Publications

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Studentship Projects

Project Reference Relationship Related To Start End Student Name
BB/M016412/1 01/10/2015 30/09/2019
1868258 Studentship BB/M016412/1 01/10/2015 30/09/2019
 
Description Generated a protocol for reproducibly directly reprogramming murine embryonic fibroblasts (MEFs) from frozen stocks into inducible thymic epithelial cells (iTEC). I have identified 13 synthetic and defined polyacrylates that are capable of supporting iTEC in monolayer culture conditions. I have developed a method of producing self-organising thymic organoids from iTEC that are capable of self-patterning into cortical and medullary regions.
Exploitation Route In the next 12 months I will uses these findings, alongside the unique technology provided by Sun Bioscience, to generate fully patterned thymic organoids that are capable of directing haematopoietic stem cells through thymopoiesis in a defined three-dimensional hydrogel environment. This work will contribute to the Blackburn laboratory's larger aim of generating self-sustaining thymic organoids in addition to the aim of generating a thymic graft for transplantation.
Sectors Healthcare,Manufacturing, including Industrial Biotechology,Pharmaceuticals and Medical Biotechnology