Imperial College London

Dr Elizabeth Want

Faculty of MedicineDepartment of Metabolism, Digestion and Reproduction

Senior Lecturer
 
 
 
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Contact

 

+44 (0)20 7594 3023e.want

 
 
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Location

 

E315CBurlington DanesHammersmith Campus

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Summary

 

Publications

Citation

BibTex format

@article{Friston:2020:10.1242/dmm.042713,
author = {Friston, D and Junttila, S and Lemes, JBP and Laycock, H and Torres-Perez, JV and Want, E and Gyenesei, A and Nagy, I},
doi = {10.1242/dmm.042713},
journal = {Dis Model Mech},
title = {Leptin and fractalkine: Novel subcutaneous cytokines in burn injury.},
url = {http://dx.doi.org/10.1242/dmm.042713},
year = {2020}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - Burn injury is a pathology underpinned by progressive and aberrant inflammation. It is a major clinical challenge to survival and quality of life. While burn injury's complex local and disseminating pathological processes ultimately stem from local tissue damage, to date relatively few studies have attempted to characterise the local inflammatory mediator profile. Here, cytokine content and associated transcriptional changes were measured in rat skin for three hours immediately following induction of a scald-type (60°C, 2 minutes) burn injury model. Leptin (p=0.0002) and fractalkine (p=0.0478) concentrations were significantly elevated post-burn above pre-burn and control site values, coinciding with the development of burn site oedema and differential expression of leptin mRNA (p=0.0004). Further, gene sequencing enrichment analysis indicated cytokine-cytokine receptor interaction (p=1.45x10-6). Subsequent behavioural studies demonstrated that, following subcutaneous injection into the dorsum of the paw, both leptin and fractalkine induced mechanical allodynia, heat hyperalgesia and the recruitment of macrophages. This is the first report of leptin's elevation specifically at the burn site and the first report of fractalkine's elevation in any tissue post-burn which, together with the functional findings, calls for exploration of the influence of these cytokines on pain, inflammation and burn wound progression. Additionally targeting these signalling molecules represents a therapeutic potential as early formative mediators of these pathological processes.
AU - Friston,D
AU - Junttila,S
AU - Lemes,JBP
AU - Laycock,H
AU - Torres-Perez,JV
AU - Want,E
AU - Gyenesei,A
AU - Nagy,I
DO - 10.1242/dmm.042713
PY - 2020///
TI - Leptin and fractalkine: Novel subcutaneous cytokines in burn injury.
T2 - Dis Model Mech
UR - http://dx.doi.org/10.1242/dmm.042713
UR - https://www.ncbi.nlm.nih.gov/pubmed/34005052
ER -