Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.733648
Title: The spatial distribution and dynamics of CXCL13 in lymphoid tissues
Author: Cosgrove, Jason
ISNI:       0000 0004 6494 3518
Awarding Body: University of York
Current Institution: University of York
Date of Award: 2017
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Abstract:
Morphogens are soluble signalling molecules that regulate a broad spectrum of biological processes. However, the distances and scales over which this regulation occurs are unclear. To date, many studies have highlighted source-sink mechanisms for morphogen gradient formation but fail to take the role of the tissue microenvironment into account. Using a systems-based approach we show that the chemokine CXCL13 is regulated by the B-cell microenvironment on distinct but interconnected levels of biological organization. CXCL13 is a key determinant of humoral immune responses, regulating the localisation of lymphocytes within lymphoid tissues. Due to a complex and dynamic interaction network occurring over broad spatiotemporal scales, mapping the spatial distribution of CXCL13 in situ is challenging. To address this we have mapped the 3-dimensional organisation of CXCL13+ stromal cells in situ using a fluorescent reporter system, identifying three distinct but interconnected stromal subsets that are unique in their network properties. We quantify CXCL13 dynamics using high-speed narrowfield microscopy in collagen matrix and lymph node tissue sections with results suggesting that diffusion is highly constrained by local tissue microanatomy. However, this data alone is insufficient to describe CXCL13 gradient formation. To consolidate this data we employ a quantitative modelling approach hybridising different techniques into a high fidelity in silico representation of the B-follicle, where immune cells can interact with stroma capable of creating and shaping complex physiological gradients. Simulation analyses and immunohistochemistry suggest that chemokine fields within the follicle are dynamic and non-uniform, with multiobjective optimization analysis suggesting that this spatial configuration is designed to promote scanning rates. Taken in concert, our data suggests that CXCL13 acts over short distances creating a complex landscape of expression. Importantly, this study provides a basis for understanding the spatial distribution of morphogens with complex binding behaviours.
Supervisor: Timmis, Jon ; Coles, Mark Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.733648  DOI: Not available
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