Cardiomyocyte Regeneration in Human Myocarditis.

STAT3 myocarditis newly generated cardiomyocytes

Journal

Biomedicines
ISSN: 2227-9059
Titre abrégé: Biomedicines
Pays: Switzerland
ID NLM: 101691304

Informations de publication

Date de publication:
09 Aug 2024
Historique:
received: 08 07 2024
revised: 02 08 2024
accepted: 04 08 2024
medline: 31 8 2024
pubmed: 31 8 2024
entrez: 29 8 2024
Statut: epublish

Résumé

Newly generated cardiomyocytes (NGCs) concur with the recovery of human myocarditis occurring spontaneously in around 50% of cases. However, NGCs decline with age, and their modality of myocardial homing and integration are still unclear. We retrospectively assessed NGCs in 213 consecutive patients with endomyocardial biopsy denoting acute myocarditis, with normal coronaries and valves. Tissue samples were processed for histology (H&E), immunohistochemistry for the evaluation of inflammatory infiltrates, immunostaining for alpha-sarcomeric-actin, junctional connexin-43, Ki-67, and phosphorylated STAT3 (p-STAT3), and Western blot (WB) for HMGB1. Frozen samples were analyzed using polymerase chain reaction (PCR) for cardiotropic viruses. Controls included 20 normal surgical biopsies. NGCs were defined as small myocytes (diameter < 10 µm) with nuclear positivity to Ki-67 and p-STAT3 and positive immunostaining for cytoplasmic α-sarcomeric actin and connexin-43. Their number/mm NGCs are constantly recognizable in acute human myocarditis. Their number declines with age. Their integration within necrotic myocytes allows for the preservation of the cardiac structure and function.

Sections du résumé

BACKGROUND BACKGROUND
Newly generated cardiomyocytes (NGCs) concur with the recovery of human myocarditis occurring spontaneously in around 50% of cases. However, NGCs decline with age, and their modality of myocardial homing and integration are still unclear.
METHODS METHODS
We retrospectively assessed NGCs in 213 consecutive patients with endomyocardial biopsy denoting acute myocarditis, with normal coronaries and valves. Tissue samples were processed for histology (H&E), immunohistochemistry for the evaluation of inflammatory infiltrates, immunostaining for alpha-sarcomeric-actin, junctional connexin-43, Ki-67, and phosphorylated STAT3 (p-STAT3), and Western blot (WB) for HMGB1. Frozen samples were analyzed using polymerase chain reaction (PCR) for cardiotropic viruses. Controls included 20 normal surgical biopsies.
RESULTS RESULTS
NGCs were defined as small myocytes (diameter < 10 µm) with nuclear positivity to Ki-67 and p-STAT3 and positive immunostaining for cytoplasmic α-sarcomeric actin and connexin-43. Their number/mm
CONCLUSIONS CONCLUSIONS
NGCs are constantly recognizable in acute human myocarditis. Their number declines with age. Their integration within necrotic myocytes allows for the preservation of the cardiac structure and function.

Identifiants

pubmed: 39200277
pii: biomedicines12081814
doi: 10.3390/biomedicines12081814
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : The study has been supported by FABRY SHIRE II, Ricerca corrente IRCCS L Spallanzani, and partially by Italian Health Ministry (IRCCS San Raffaele Roma-Ricerca Corrente #2020/1)
ID : s

Auteurs

Andrea Frustaci (A)

Cellular and Molecular Cardiology Lab, IRCCS L. Spallanzani, Via Portuense, 292, 00149 Rome, Italy.

Eleonora Foglio (E)

Technoscience, Parco Scientifico e Tecnologico Pontino, 04100 Latina, Italy.

Federica Limana (F)

Department of Human Sciences and Promotion of Quality of Life, San Raffaele University of Rome, IRCCS San Raffaele, 00163 Rome, Italy.

Michele Magnocavallo (M)

Arrhythmology Unit, Ospedale Isola Tiberina-Gemelli Isola, 00186 Rome, Italy.

Emanuela Frustaci (E)

Technoscience, Parco Scientifico e Tecnologico Pontino, 04100 Latina, Italy.
Department of Molecular Medicine, Sapienza University of Rome, 00185 Rome, Italy.
MEBIC Consortium, IRCCS San Raffaele Roma, 00163 Rome, Italy.

Leonardo Lupacchini (L)

Laboratory of Molecular and Cellular Neuroscience, IRCCS San Raffaele Roma, 00163 Rome, Italy.

Romina Verardo (R)

Cellular and Molecular Cardiology Lab, IRCCS L. Spallanzani, Via Portuense, 292, 00149 Rome, Italy.

Classifications MeSH