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Signalling pathways involved in ribonuclease-7 expression

Mohammed, Imran; Yeung, Aaron; Abedin, Asiya; Hopkinson, Andrew; Dua, Harminder S.

Authors

Imran Mohammed

Aaron Yeung

Asiya Abedin

Andrew Hopkinson

HARMINDER DUA HARMINDER.DUA@NOTTINGHAM.AC.UK
Professor of Ophthalmology and Visual Sciences



Abstract

Antimicrobial peptides are host defence molecules that play a potential role in preventing infection at the epithelial surfaces. Ribonuclease (RNase)-7 has been shown to possess a broad spectrum of microbicidal activity against various pathogens. Here, we demonstrate that RNase-7 protein is localised to the superficial layers of ocular surface cells and increased in response to interleukin (IL)-1?, suggesting an active role during inflammation related to ocular surface infection. Signal transduction pathways involved in RNase-7 expression are unknown. Involvement of transforming growth factor ?-activated kinase-1 (TAK-1) activated nuclear factor kappa B (NF-?B) and mitogen-activated protein kinase (MAPK) pathway molecules [c-Jun N-terminal kinase (JNK), extracellular signal-regulated kinase (ERK) and p38] were studied because of their importance in infection and inflammation. Blocking the MAPKs resulted in inhibition of RNase-7 expression in response to IL-1?. However, RNase-7 induction by IL-1? was not affected by inhibiting the NF-?B signalling pathway. In conclusion, our results indicate that RNase-7 expression is specifically mediated via MAPKs but not NF-?B signalling pathways.

Journal Article Type Article
Acceptance Date Sep 27, 2010
Online Publication Date Oct 22, 2010
Publication Date 2011-06
Deposit Date Jul 21, 2020
Journal Cellular and Molecular Life Sciences
Print ISSN 1420-682X
Electronic ISSN 1420-9071
Publisher Springer Verlag
Peer Reviewed Peer Reviewed
Volume 68
Issue 11
Pages 1941-1952
DOI https://doi.org/10.1007/s00018-010-0540-2
Keywords Molecular Medicine; Cell Biology; Molecular Biology; Pharmacology; Cellular and Molecular Neuroscience
Public URL https://nottingham-repository.worktribe.com/output/4781051
Publisher URL https://link.springer.com/article/10.1007/s00018-010-0540-2