Literature DB >> 26509590

Long wavelength multiphoton excitation is advantageous for intravital kidney imaging.

C D Schuh, D Haenni, E Craigie, U Ziegler, B Weber, O Devuyst, Andrew M Hall.   

Abstract

Intravital multiphoton microscopy is a powerful tool to study kidney physiology in living animals. However, certain technical issues have curbed its usage to date, including limited depth of tissue penetration and high background emission of endogenous signals. Most previous studies have used the excitation range 700–1000 nm. Since newer longer wavelength excitation lasers may provide solutions to these problems we constructed a microscope coupled to a laser tunable up to 1300 nm and optimized for kidney imaging. This set-up offers substantial advantages for intravital studies, especially when coupled with newly available far-red probes. First, the background at longer wavelengths is markedly reduced, thus increasing the signal to background ratio. Second, the depth of tissue penetration is significantly increased, enabling detailed imaging of previously inaccessible structures, such as deeper glomeruli. Third, using a combination of two- and three-photon excitation, multiple different fluorescent probes can be imaged simultaneously in the same animal, with clear spectral separation. Application of these techniques helped visualize pathological aspects of tubular cell function in a well-established model of acute kidney injury (maleate toxicity). Thus, utilizing long wavelength excitation offers substantial advantages for intravital kidney imaging, which together enhance the capabilities of this powerful and increasingly used research technique.

Entities:  

Mesh:

Substances:

Year:  2016        PMID: 26509590     DOI: 10.1038/ki.2015.323

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  20 in total

1.  Design and performance of an ultra-flexible two-photon microscope for in vivo research.

Authors:  Johannes M Mayrhofer; Florent Haiss; Dominik Haenni; Stefan Weber; Marc Zuend; Matthew J P Barrett; Kim David Ferrari; Philipp Maechler; Aiman S Saab; Jillian L Stobart; Matthias T Wyss; Helge Johannssen; Harald Osswald; Lucy M Palmer; Vincent Revol; Claus-Dieter Schuh; Claus Urban; Andrew Hall; Matthew E Larkum; Edith Rutz-Innerhofer; Hanns Ulrich Zeilhofer; Urs Ziegler; Bruno Weber
Journal:  Biomed Opt Express       Date:  2015-10-02       Impact factor: 3.732

2.  Combined Structural and Functional Imaging of the Kidney Reveals Major Axial Differences in Proximal Tubule Endocytosis.

Authors:  Claus D Schuh; Marcello Polesel; Evgenia Platonova; Dominik Haenni; Alkaly Gassama; Natsuko Tokonami; Susan Ghazi; Milica Bugarski; Olivier Devuyst; Urs Ziegler; Andrew M Hall
Journal:  J Am Soc Nephrol       Date:  2018-10-09       Impact factor: 10.121

3.  Multiphoton imaging reveals axial differences in metabolic autofluorescence signals along the kidney proximal tubule.

Authors:  Milica Bugarski; Joana Raquel Martins; Dominik Haenni; Andrew M Hall
Journal:  Am J Physiol Renal Physiol       Date:  2018-08-22

Review 4.  Deep insights: intravital imaging with two-photon microscopy.

Authors:  Ina Maria Schießl; Hayo Castrop
Journal:  Pflugers Arch       Date:  2016-06-28       Impact factor: 3.657

Review 5.  Advances in Renal Cell Imaging.

Authors:  Georgina Gyarmati; Hiroyuki Kadoya; Ju-Young Moon; James L Burford; Nariman Ahmadi; Inderbir S Gill; Young-Kwon Hong; Bálint Dér; János Peti-Peterdi
Journal:  Semin Nephrol       Date:  2018-01       Impact factor: 5.299

Review 6.  In vivo microscopy.

Authors:  János Peti-Peterdi
Journal:  Nephrol Ther       Date:  2016-03-08       Impact factor: 0.722

7.  Spectral Characteristics of Autofluorescence in Renal Tissue and Methods for Reducing Fluorescence Background in Confocal Laser Scanning Microscopy.

Authors:  Yang Zhang; Yang Wang; Wei-Wei Cao; Ke-Tao Ma; Wei Ji; Zi-Wei Han; Jun-Qiang Si; Li Li
Journal:  J Fluoresc       Date:  2018-03-20       Impact factor: 2.217

Review 8.  Just Look! Intravital Microscopy as the Best Means to Study Kidney Cell Death Dynamics.

Authors:  Ina Maria Schießl; Anna Hammer; Anne Riquier-Brison; Janos Peti-Peterdi
Journal:  Semin Nephrol       Date:  2016-05       Impact factor: 5.299

9.  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

Review 10.  Intravital imaging in the kidney.

Authors:  János Peti-Peterdi; Kengo Kidokoro; Anne Riquier-Brison
Journal:  Curr Opin Nephrol Hypertens       Date:  2016-05       Impact factor: 2.894

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.