Evidence map›Paper›PMID 39535377›Full record

ArticleESC heart failure2025

CardiLect: A combined cross-species lectin histochemistry protocol for the automated analysis of cardiac remodelling.

Tamás G Gergely, Tamás Kovács, Andrea Kovács, Viktória E Tóth, Nabil V Sayour, Gábor M Mórotz, Csenger Kovácsházi, Gábor B Brenner, Zsófia Onódi, Balázs Enyedi and 5 more

Abstract read
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Article in ESC heart failure, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors.

Tamás G GergelyDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Tamás KovácsDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Andrea KovácsDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Viktória E TóthDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Nabil V SayourDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Gábor M MórotzDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Csenger KovácsháziDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Gábor B BrennerDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Zsófia OnódiDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Balázs EnyediDepartment of Physiology, Faculty of Medicine, Semmelweis University, Tűzoltó utca 37-47, H-1094, Budapest, Hungary.
Domokos MáthéDepartment of Biophysics and Radiation Biology, Faculty of Medicine, Semmelweis University, Budapest, Hungary.
Przemyslaw LeszekDepartment of Heart Failure and Transplantology, Cardinal Stefan Wyszyński Institute of Cardiology, 04-628, Warszawa, Poland.
Zoltán GiriczDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Péter FerdinandyDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.
Zoltán V VargaDepartment of Pharmacology and Pharmacotherapy, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0000-0002-2758-0784

Funding

European Union 739593Gedeon Richter Talentum FoundationJános Bolyai Research Fellowship of the Hungarian Academy of Sciences BO/00277/23/5Ministry for Innovation and Technology 2020-4.1.1.-TKP2020National Research, Development and Innovation Fund ÚNKP-23-4-I-SE-5National Research, Development and Innovation Fund ÚNKP-23-5-SE-9National Research, Development and Innovation Fund ÚNKP-23-II-SE-43National Research, Development and Innovation Office FK134751National Research, Development and Innovation Office FK146163
6 · The paper itself

Abstract

backgroundCardiac remodelling, a crucial aspect of heart failure, is commonly investigated in preclinical models by quantifying cardiomyocyte cross-sectional area (CSA) and microvascular density (MVD) via histological methods, such as immunohistochemistry. To achieve this, optimized protocols are needed, and the species specificity is dependent on the antibody used. Lectin histochemistry offers several advantages compared to antibody-based immunohistochemistry, including as cost-effectiveness and cross-species applicability. Direct comparisons between the two methods are lacking from the literature. METHODS AND

resultsIn this study, we compared antibody- and lectin-based methods for the histological assessment of cardiomyocyte CSA (with the use of anti-laminin and wheat germ agglutinin [WGA]) and microvascular density (utilizing anti-CD31 and isolectin B4 [ILB4]) using different embedding and antigen/carbohydrate retrieval techniques. Here, we describe a detailed, easy-to-use combined lectin histochemistry protocol (WGA and ILB4, 'CardiLect' protocol) for the histological assessment of cardiac remodelling. The lectin-based approach has been evaluated on a cross-species basis, and its efficacy has been demonstrated in zebrafish, rodents, large animals and human samples. We provide an ImageJ script ('CardiLect Analyser') for automated image analysis, validated in a preclinical heart failure model by correlating histological parameters with echocardiographic findings. CSA showed a significant positive correlation with left ventricular (LV) mass (P = 0.0098, r

conclusionsThe described combined lectin histochemistry protocol with the provided ImageJ script is an easy-to-use, cost-effective, cross-species approach for the histological assessment of cardiac remodelling.

Indexed as

Heart FailureLectinsMyocytes, CardiacVentricular RemodelingAnimalsDisease Models, AnimalHumansImmunohistochemistryMaleRatsLectinsCardiac remodellingEchocardiographyHeart failureImmunohistochemistryLectinTransverse aortic constriction

Identifiers

PMID39535377
PMCPMC11911624

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.