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

Cell Rep. 2017 Oct 3;21(1):274-288. doi: 10.1016/j.celrep.2017.09.022.

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.

Keywords: FLIM-FRET; actin; biosensors; breast cancer; cell biology; development; immunology; intravital imaging; pancreatic cancer; small GTPase RhoA.

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Biosensing Techniques*
  • Bone and Bones / cytology
  • Bone and Bones / metabolism
  • Cell Movement / drug effects
  • Dasatinib / pharmacology
  • Erlotinib Hydrochloride / pharmacology
  • Female
  • Fluorescence Resonance Energy Transfer / instrumentation
  • Fluorescence Resonance Energy Transfer / methods*
  • Gene Expression Regulation
  • Intestine, Small / metabolism
  • Intestine, Small / ultrastructure
  • Intravital Microscopy / instrumentation
  • Intravital Microscopy / methods*
  • Mammary Glands, Animal / blood supply
  • Mammary Glands, Animal / drug effects
  • Mammary Glands, Animal / ultrastructure
  • Mammary Neoplasms, Experimental / blood supply
  • Mammary Neoplasms, Experimental / drug therapy
  • Mammary Neoplasms, Experimental / genetics
  • Mammary Neoplasms, Experimental / ultrastructure
  • Mechanotransduction, Cellular
  • Mice
  • Mice, Transgenic
  • Neutrophils / metabolism
  • Neutrophils / ultrastructure
  • Osteocytes / metabolism
  • Osteocytes / ultrastructure
  • Pancreatic Neoplasms / blood supply
  • Pancreatic Neoplasms / drug therapy
  • Pancreatic Neoplasms / genetics
  • Pancreatic Neoplasms / ultrastructure
  • Time-Lapse Imaging / instrumentation
  • Time-Lapse Imaging / methods*
  • rho GTP-Binding Proteins / genetics*
  • rho GTP-Binding Proteins / metabolism
  • rhoA GTP-Binding Protein

Substances

  • Antineoplastic Agents
  • Erlotinib Hydrochloride
  • RhoA protein, mouse
  • rho GTP-Binding Proteins
  • rhoA GTP-Binding Protein
  • Dasatinib