Literature DB >> 26968479

In vivo microscopy.

János Peti-Peterdi1.   

Abstract

This article summarizes the past, present, and future promise of multiphoton excitation fluorescence microscopy for intravital kidney imaging. During the past 15years, several high-power visual research approaches have been developed using multiphoton imaging to study the normal functions of the healthy, intact, living kidney, and the various molecular and cellular mechanisms of the development of kidney diseases. In this review, the main focus will be on intravital multiphoton imaging of the glomerulus, the structure and function of the glomerular filtration barrier, especially the podocyte. Examples will be given for the combination of two powerful research tools, in vivo multiphoton imaging and mouse genetics using commercially available whole animal models for the detailed characterization of glomerular cell types, their function and fate, and for the better understanding of the molecular mechanisms of glomerular pathologies. One of the new modalities of multiphoton imaging, serial imaging of the same glomerulus in the same animal over several days will be emphasized for its potential for further advancing the field of nephrology research.
Copyright © 2016 Association Société de néphrologie. Published by Elsevier SAS. All rights reserved.

Entities:  

Keywords:  Albumin leakage; Confetti construct; GCaMP; Glomerular filtration barrier; Multiphoton microscopy; Podocyte; Purinergic signaling

Mesh:

Year:  2016        PMID: 26968479      PMCID: PMC4893902          DOI: 10.1016/j.nephro.2016.01.004

Source DB:  PubMed          Journal:  Nephrol Ther        ISSN: 1769-7255            Impact factor:   0.722


  40 in total

1.  Two-photon excitation fluorescence imaging of the living juxtaglomerular apparatus.

Authors:  János Peti-Peterdi; Shigeru Morishima; P Darwin Bell; Yasunobu Okada
Journal:  Am J Physiol Renal Physiol       Date:  2002-07

2.  Long wavelength multiphoton excitation is advantageous for intravital kidney imaging.

Authors:  C D Schuh; D Haenni; E Craigie; U Ziegler; B Weber; O Devuyst; Andrew M Hall
Journal:  Kidney Int       Date:  2016-03       Impact factor: 10.612

Review 3.  Deep tissue two-photon microscopy.

Authors:  Fritjof Helmchen; Winfried Denk
Journal:  Nat Methods       Date:  2005-12       Impact factor: 28.547

4.  The normal kidney filters nephrotic levels of albumin retrieved by proximal tubule cells: retrieval is disrupted in nephrotic states.

Authors:  L M Russo; R M Sandoval; M McKee; T M Osicka; A B Collins; D Brown; B A Molitoris; W D Comper
Journal:  Kidney Int       Date:  2007-01-17       Impact factor: 10.612

Review 5.  Two-photon microscopy: visualization of kidney dynamics.

Authors:  S L Ashworth; R M Sandoval; G A Tanner; B A Molitoris
Journal:  Kidney Int       Date:  2007-05-30       Impact factor: 10.612

Review 6.  Potential solutions for confocal imaging of living animals.

Authors:  Claudette St Croix; Warren R Zipfel; Simon C Watkins
Journal:  Biotechniques       Date:  2007-07       Impact factor: 1.993

Review 7.  Dynamic multiphoton microscopy: focusing light on acute kidney injury.

Authors:  Andrew M Hall; Bruce A Molitoris
Journal:  Physiology (Bethesda)       Date:  2014-09

8.  Intravital imaging of podocyte calcium in glomerular injury and disease.

Authors:  James L Burford; Karie Villanueva; Lisa Lam; Anne Riquier-Brison; Matthias J Hackl; Jeffrey Pippin; Stuart J Shankland; János Peti-Peterdi
Journal:  J Clin Invest       Date:  2014-04-08       Impact factor: 14.808

9.  Angiotensin II AT2 receptor activation attenuates AT1 receptor-induced increases in the glomerular filtration of albumin: a multiphoton microscopy study.

Authors:  Ina Maria Schießl; Hayo Castrop
Journal:  Am J Physiol Renal Physiol       Date:  2013-08-14

10.  Tracking the fate of glomerular epithelial cells in vivo using serial multiphoton imaging in new mouse models with fluorescent lineage tags.

Authors:  Matthias J Hackl; James L Burford; Karie Villanueva; Lisa Lam; Katalin Suszták; Bernhard Schermer; Thomas Benzing; János Peti-Peterdi
Journal:  Nat Med       Date:  2013-11-24       Impact factor: 53.440

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  1 in total

1.  Novel fluorescence techniques to quantitate renal cell biology.

Authors:  Urvi Nikhil Shroff; Ina Maria Schiessl; Georgina Gyarmati; Anne Riquier-Brison; Janos Peti-Peterdi
Journal:  Methods Cell Biol       Date:  2019-05-17       Impact factor: 1.441

  1 in total

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