Volume 35, Issue 5 e21595
METHODS
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Assessment of renal fibrosis and anti-fibrotic agents using a novel diagnostic and stain-free second-harmonic generation platform

Sadman Bhuiyan

Sadman Bhuiyan

Cardiovascular Disease Program, Monash Biomedicine Discovery Institute and Department of Pharmacology, Monash University, Melbourne, VIC, Australia

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Matthew Shen

Matthew Shen

Cardiovascular Disease Program, Monash Biomedicine Discovery Institute and Department of Pharmacology, Monash University, Melbourne, VIC, Australia

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Sharenya Chelvaretnam

Sharenya Chelvaretnam

Cardiovascular Disease Program, Monash Biomedicine Discovery Institute and Department of Pharmacology, Monash University, Melbourne, VIC, Australia

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Andre Y. Tan

Andre Y. Tan

HistoIndex Pte Ltd, The LaunchPad, Fusionopolis, Singapore

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Gideon Ho

Gideon Ho

HistoIndex Pte Ltd, The LaunchPad, Fusionopolis, Singapore

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Mohammed Akhter Hossain

Mohammed Akhter Hossain

Florey Institute for Neuroscience and Mental Health, The University of Melbourne, Melbourne, VIC, Australia

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Robert E. Widdop

Corresponding Author

Robert E. Widdop

Cardiovascular Disease Program, Monash Biomedicine Discovery Institute and Department of Pharmacology, Monash University, Melbourne, VIC, Australia

Correspondence

Robert E. Widdop and Chrishan S. Samuel, Department of Pharmacology, Monash University, Clayton, Melbourne, VIC 3800, Australia.

Email: [email protected] (R.E. W.); [email protected] (C.S. S.)

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Chrishan S. Samuel

Corresponding Author

Chrishan S. Samuel

Cardiovascular Disease Program, Monash Biomedicine Discovery Institute and Department of Pharmacology, Monash University, Melbourne, VIC, Australia

Department of Biochemistry and Molecular Biology, The University of Melbourne, Melbourne, VIC, Australia

Correspondence

Robert E. Widdop and Chrishan S. Samuel, Department of Pharmacology, Monash University, Clayton, Melbourne, VIC 3800, Australia.

Email: [email protected] (R.E. W.); [email protected] (C.S. S.)

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First published: 28 April 2021
Citations: 5

Abstract

Current histological measurement techniques for interstitial collagen, the basis of interstitial fibrosis, are semi-quantitative at best and only provide a ratio of collagen levels within tissues. The Genesis200 imaging system and supplemental image analysis software, FibroIndex from HistoIndex, is a novel, automated platform that uses second-harmonic generation (SHG) for imaging and characterization of interstitial collagen deposition and additional characteristics, in the absence of any staining. However, its ability to quantify renal fibrosis requires investigation. This study compared SHG imaging of renal fibrosis in mice with unilateral ureteric obstruction (UUO), to that of Masson’s trichrome staining (MTS) and immunohistochemistry (IHC) of collagen I. Additionally, the platform generated data on collagen morphology and distribution patterns. While all three methods determined that UUO-injured mice underwent significantly increased renal fibrosis after 7 days, the HistoIndex platform additionally determined that UUO-injured mice had a significantly increased collagen-to-tissue cross reticulation ratio (all P < .001 vs sham group). Furthermore, in UUO-injured mice treated with the relaxin family peptide receptor-1 agonists, relaxin (0.5 mg/kg/day) or B7-33 (0.25 mg/kg/day), or angiotensin converting enzyme-inhibitor, perindopril (1 mg/kg/day) over the 7-day period, only the HistoIndex platform determined that the drug-induced prevention of renal fibrosis correlated with significantly reduced collagen fiber thickness and collagen-to-tissue cross reticulation ratio, but increased collagen fiber counts. Relaxin or B7-33 treatment also increased renal matrix metalloproteinase-2 and reduced tissue inhibitor of metalloproteinase-1 levels (all P < .01 vs UUO alone). This study demonstrated the diagnostic value of the HistoIndex platform over currently used staining techniques.

CONFLICTS OF INTEREST

All other authors declare no conflicts of interest.