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A RhoA-FRET Biosensor Mouse for Intravital Imaging in Normal Tissue Homeostasis and Disease Contexts

Authors :
Max Nobis
Tatyana Chtanova
Marina Pajic
Douglas Strathdee
Peter W. Gunning
Stacey N. Walters
Peter I. Croucher
Juliane P. Schwarz
Edna C. Hardeman
Julian M. W. Quinn
Kurt I. Anderson
Alice Boulghourjian
Agata Mrowinska
James R.W. Conway
Owen J. Sansom
Christopher J. Ormandy
Nadine Reischmann
David Herrmann
Paul Timpson
Monica J. Killen
Heidi C.E. Welch
Lei Zhang
Jennifer P. Morton
Michael S. Samuel
Andrius Masedunskas
Claire Vennin
Paul A. Baldock
Shereen Kadir
Jacqueline Bailey
Anna-Karin E. Johnsson
Richard P. Harvey
Andrew M. K. Law
Wilfred Leung
Ewan J. McGhee
Morghan C. Lucas
Gonzalo del Monte-Nieto
Anaiis Zaratzian
Herbert Herzog
Astrid Magenau
David A. Stevenson
Shane T. Grey
Sean C. Warren
David Gallego-Ortega
Killen, Monica [0000-0001-9832-0421]
Welch, Heidi Christine Erika [0000-0001-7865-7000]
Apollo - University of Cambridge Repository
Nobis, Max
Herrmann, David
Warren, Sean C
Kadir, Shereen
Samuel, Michael S
Timpson, Paul
Source :
Cell Reports, Vol 21, Iss 1, Pp 274-288 (2017)
Publication Year :
2019
Publisher :
Elsevier BV, 2019.

Abstract

The small GTPase RhoA is involved in a variety of fundamental processes in normal tissue. Spatiotemporal control of RhoA is thought to govern mechanosensing, growth, and motility of cells, while its deregulation is associated with disease development. Here, we describe the generation of a RhoA-fluorescence resonance energy transfer (FRET) biosensor mouse and its utility for monitoring real-time activity of RhoA in a variety of native tissues in vivo. We assess changes in RhoA activity during mechanosensing of osteocytes within the bone and during neutrophil migration. We also demonstrate spatiotemporal order of RhoA activity within crypt cells of the small intestine and during different stages of mammary gestation. Subsequently, we reveal co-option of RhoA activity in both invasive breast and pancreatic cancers, and we assess drug targeting in these disease settings, illustrating the potential for utilizing this mouse to study RhoA activity in vivo in real time. Nobis et al. generated a RhoA-FRET biosensor mouse to characterize and quantify the spatiotemporal distribution of RhoA activity in native mammalian tissues in vivo during development and disease progression. They show that RhoA activity is tightly regulated during various normal biological processes and is co-opted in disease settings, such as invasive breast and pancreatic cancers. Refereed/Peer-reviewed

Details

ISSN :
22111247
Database :
OpenAIRE
Journal :
Cell Reports, Vol 21, Iss 1, Pp 274-288 (2017)
Accession number :
edsair.doi.dedup.....4b5ae14f85f6dbaec756cfb97ddafd72
Full Text :
https://doi.org/10.17863/cam.41203