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Polyploid tubular cells initiate a TGF-β1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury

Polyploidization of tubular cells (TC) is triggered by acute kidney injury (AKI) to allow survival in the early phase after AKI, but in the long run promotes fibrosis and AKI-chronic kidney disease (CKD) transition. The molecular mechanism governing the link between polyploid TC and kidney fibrosis...

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Autores principales: De Chiara, Letizia, Semeraro, Roberto, Mazzinghi, Benedetta, Landini, Samuela, Molli, Alice, Antonelli, Giulia, Angelotti, Maria Lucia, Melica, Maria Elena, Maggi, Laura, Conte, Carolina, Peired, Anna Julie, Cirillo, Luigi, Raglianti, Valentina, Magi, Alberto, Annunziato, Francesco, Romagnani, Paola, Lazzeri, Elena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Physiological Society 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10635654/
https://www.ncbi.nlm.nih.gov/pubmed/37642236
http://dx.doi.org/10.1152/ajpcell.00081.2023
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author De Chiara, Letizia
Semeraro, Roberto
Mazzinghi, Benedetta
Landini, Samuela
Molli, Alice
Antonelli, Giulia
Angelotti, Maria Lucia
Melica, Maria Elena
Maggi, Laura
Conte, Carolina
Peired, Anna Julie
Cirillo, Luigi
Raglianti, Valentina
Magi, Alberto
Annunziato, Francesco
Romagnani, Paola
Lazzeri, Elena
author_facet De Chiara, Letizia
Semeraro, Roberto
Mazzinghi, Benedetta
Landini, Samuela
Molli, Alice
Antonelli, Giulia
Angelotti, Maria Lucia
Melica, Maria Elena
Maggi, Laura
Conte, Carolina
Peired, Anna Julie
Cirillo, Luigi
Raglianti, Valentina
Magi, Alberto
Annunziato, Francesco
Romagnani, Paola
Lazzeri, Elena
author_sort De Chiara, Letizia
collection PubMed
description Polyploidization of tubular cells (TC) is triggered by acute kidney injury (AKI) to allow survival in the early phase after AKI, but in the long run promotes fibrosis and AKI-chronic kidney disease (CKD) transition. The molecular mechanism governing the link between polyploid TC and kidney fibrosis remains to be clarified. In this study, we demonstrate that immediately after AKI, expression of cell cycle markers mostly identifies a population of DNA-damaged polyploid TC. Using transgenic mouse models and single-cell RNA sequencing we show that, unlike diploid TC, polyploid TC accumulate DNA damage and survive, eventually resting in the G1 phase of the cell cycle. In vivo and in vitro single-cell RNA sequencing along with sorting of polyploid TC shows that these cells acquire a profibrotic phenotype culminating in transforming growth factor (TGF)-β1 expression and that TGF-β1 directly promotes polyploidization. This demonstrates that TC polyploidization is a self-sustained mechanism. Interactome analysis by single-cell RNA sequencing revealed that TGF-β1 signaling fosters a reciprocal activation loop among polyploid TC, macrophages, and fibroblasts to sustain kidney fibrosis and promote CKD progression. Collectively, this study contributes to the ongoing revision of the paradigm of kidney tubule response to AKI, supporting the existence of a tubulointerstitial cross talk mediated by TGF-β1 signaling produced by polyploid TC following DNA damage. NEW & NOTEWORTHY Polyploidization in tubular epithelial cells has been neglected until recently. Here, we showed that polyploidization is a self-sustained mechanism that plays an important role during chronic kidney disease development, proving the existence of a cross talk between infiltrating cells and polyploid tubular cells. This study contributes to the ongoing revision of kidney adaptation to injury, posing polyploid tubular cells at the center of the process.
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spelling pubmed-106356542023-11-15 Polyploid tubular cells initiate a TGF-β1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury De Chiara, Letizia Semeraro, Roberto Mazzinghi, Benedetta Landini, Samuela Molli, Alice Antonelli, Giulia Angelotti, Maria Lucia Melica, Maria Elena Maggi, Laura Conte, Carolina Peired, Anna Julie Cirillo, Luigi Raglianti, Valentina Magi, Alberto Annunziato, Francesco Romagnani, Paola Lazzeri, Elena Am J Physiol Cell Physiol Research Article Polyploidization of tubular cells (TC) is triggered by acute kidney injury (AKI) to allow survival in the early phase after AKI, but in the long run promotes fibrosis and AKI-chronic kidney disease (CKD) transition. The molecular mechanism governing the link between polyploid TC and kidney fibrosis remains to be clarified. In this study, we demonstrate that immediately after AKI, expression of cell cycle markers mostly identifies a population of DNA-damaged polyploid TC. Using transgenic mouse models and single-cell RNA sequencing we show that, unlike diploid TC, polyploid TC accumulate DNA damage and survive, eventually resting in the G1 phase of the cell cycle. In vivo and in vitro single-cell RNA sequencing along with sorting of polyploid TC shows that these cells acquire a profibrotic phenotype culminating in transforming growth factor (TGF)-β1 expression and that TGF-β1 directly promotes polyploidization. This demonstrates that TC polyploidization is a self-sustained mechanism. Interactome analysis by single-cell RNA sequencing revealed that TGF-β1 signaling fosters a reciprocal activation loop among polyploid TC, macrophages, and fibroblasts to sustain kidney fibrosis and promote CKD progression. Collectively, this study contributes to the ongoing revision of the paradigm of kidney tubule response to AKI, supporting the existence of a tubulointerstitial cross talk mediated by TGF-β1 signaling produced by polyploid TC following DNA damage. NEW & NOTEWORTHY Polyploidization in tubular epithelial cells has been neglected until recently. Here, we showed that polyploidization is a self-sustained mechanism that plays an important role during chronic kidney disease development, proving the existence of a cross talk between infiltrating cells and polyploid tubular cells. This study contributes to the ongoing revision of kidney adaptation to injury, posing polyploid tubular cells at the center of the process. American Physiological Society 2023-10-01 2023-08-29 /pmc/articles/PMC10635654/ /pubmed/37642236 http://dx.doi.org/10.1152/ajpcell.00081.2023 Text en The Authors. https://creativecommons.org/licenses/by/4.0/Licensed under Creative Commons Attribution CC-BY 4.0 (https://creativecommons.org/licenses/by/4.0/) . Published by the American Physiological Society.
spellingShingle Research Article
De Chiara, Letizia
Semeraro, Roberto
Mazzinghi, Benedetta
Landini, Samuela
Molli, Alice
Antonelli, Giulia
Angelotti, Maria Lucia
Melica, Maria Elena
Maggi, Laura
Conte, Carolina
Peired, Anna Julie
Cirillo, Luigi
Raglianti, Valentina
Magi, Alberto
Annunziato, Francesco
Romagnani, Paola
Lazzeri, Elena
Polyploid tubular cells initiate a TGF-β1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury
title Polyploid tubular cells initiate a TGF-β1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury
title_full Polyploid tubular cells initiate a TGF-β1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury
title_fullStr Polyploid tubular cells initiate a TGF-β1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury
title_full_unstemmed Polyploid tubular cells initiate a TGF-β1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury
title_short Polyploid tubular cells initiate a TGF-β1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury
title_sort polyploid tubular cells initiate a tgf-β1 controlled loop that sustains polyploidization and fibrosis after acute kidney injury
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10635654/
https://www.ncbi.nlm.nih.gov/pubmed/37642236
http://dx.doi.org/10.1152/ajpcell.00081.2023
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