B-cells within lymph nodes are exposed to cell-to-cell interactions, and mutliple cytokines.

BBSRC · United Kingdom government procurement

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September 29, 2028
Response Due
Active
Status

Opportunity Overview

These signals are interpreted by molecular signalling pathways such as the NF-KB signalling pathway, and in response B-cells can secrete cytokines and chemokines to potentially remodel their micro-environment. The goal of this project is to understand this bi-directional relationship between B-cells and their microenvironment, and how mutations may impact signalling and cytokine secretion. Signal rewiring by mutations has important implications for cancer, immunotherapies, inflammation and auto-immunity.

This project will address this challenge using interdisciplinary systems biology approaches including computational modelling, experimental wet-lab work in cell lines, and validation in primary patient material and murine models.

Our computational/in vitro preliminary data suggests that mutations can re-wire the NF-KB signalling pathway, creating crosstalk between pro-survival/developmental signalling and pro-inflammatory signalling. One impact of this signalling crosstalk may be that mutated cells respond incorrectly to their microenvironment, and produce a pro-inflammatory response to pro-survival/developmental signals, resulting in microenvironment remodelling.

The student will perform computational modelling that predicts how mutations might alter the way B-cells cells interpret their environment. This work will leverage vast data available from cancer studies that spans the scales from mutations to outcomes. These predictions will then be tested in cell lines by measuring NF-KB activity and the cytokines expressed in mutated and unmutated cells using a combination of transfection/CRISPR-cas9 experiments to introduce mutated genes/knock-out genes respectively. Exciting results from the lab will be carried forward to lymph node biopsy samples, and cell line-derived xenograft models where cell lines with/without cross-talk driving mutations will be introduced and immune infiltration will be assayed using spectral flow cytometry.

Computational modelling...

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Solicitation Details

Issuing agencyBBSRC
CountryUnited Kingdom
CategoryResearch Development
PublishedSeptember 30, 2024
Procurement stageActive solicitation
Response dueSeptember 29, 2028
StatusOpen — accepting responses
Official sourceView original notice
Last verifiedAugust 09, 2026

Source: UK Research and Innovation (UKRI) — Open Government Licence v3.0.

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