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Imaging the Renal Microcirculation in Cell Therapy

Renal microvascular rarefaction plays a pivotal role in progressive kidney disease. Therefore, modalities to visualize the microcirculation of the kidney will increase our understanding of disease mechanisms and consequently may provide new approaches for evaluating cell-based therapy. At the moment...

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Detalles Bibliográficos
Autores principales: Apelt, Katerina, Bijkerk, Roel, Lebrin, Franck, Rabelink, Ton J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147454/
https://www.ncbi.nlm.nih.gov/pubmed/34063200
http://dx.doi.org/10.3390/cells10051087
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author Apelt, Katerina
Bijkerk, Roel
Lebrin, Franck
Rabelink, Ton J.
author_facet Apelt, Katerina
Bijkerk, Roel
Lebrin, Franck
Rabelink, Ton J.
author_sort Apelt, Katerina
collection PubMed
description Renal microvascular rarefaction plays a pivotal role in progressive kidney disease. Therefore, modalities to visualize the microcirculation of the kidney will increase our understanding of disease mechanisms and consequently may provide new approaches for evaluating cell-based therapy. At the moment, however, clinical practice is lacking non-invasive, safe, and efficient imaging modalities to monitor renal microvascular changes over time in patients suffering from renal disease. To emphasize the importance, we summarize current knowledge of the renal microcirculation and discussed the involvement in progressive kidney disease. Moreover, an overview of available imaging techniques to uncover renal microvascular morphology, function, and behavior is presented with the associated benefits and limitations. Ultimately, the necessity to assess and investigate renal disease based on in vivo readouts with a resolution up to capillary level may provide a paradigm shift for diagnosis and therapy in the field of nephrology.
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spelling pubmed-81474542021-05-26 Imaging the Renal Microcirculation in Cell Therapy Apelt, Katerina Bijkerk, Roel Lebrin, Franck Rabelink, Ton J. Cells Review Renal microvascular rarefaction plays a pivotal role in progressive kidney disease. Therefore, modalities to visualize the microcirculation of the kidney will increase our understanding of disease mechanisms and consequently may provide new approaches for evaluating cell-based therapy. At the moment, however, clinical practice is lacking non-invasive, safe, and efficient imaging modalities to monitor renal microvascular changes over time in patients suffering from renal disease. To emphasize the importance, we summarize current knowledge of the renal microcirculation and discussed the involvement in progressive kidney disease. Moreover, an overview of available imaging techniques to uncover renal microvascular morphology, function, and behavior is presented with the associated benefits and limitations. Ultimately, the necessity to assess and investigate renal disease based on in vivo readouts with a resolution up to capillary level may provide a paradigm shift for diagnosis and therapy in the field of nephrology. MDPI 2021-05-02 /pmc/articles/PMC8147454/ /pubmed/34063200 http://dx.doi.org/10.3390/cells10051087 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Apelt, Katerina
Bijkerk, Roel
Lebrin, Franck
Rabelink, Ton J.
Imaging the Renal Microcirculation in Cell Therapy
title Imaging the Renal Microcirculation in Cell Therapy
title_full Imaging the Renal Microcirculation in Cell Therapy
title_fullStr Imaging the Renal Microcirculation in Cell Therapy
title_full_unstemmed Imaging the Renal Microcirculation in Cell Therapy
title_short Imaging the Renal Microcirculation in Cell Therapy
title_sort imaging the renal microcirculation in cell therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8147454/
https://www.ncbi.nlm.nih.gov/pubmed/34063200
http://dx.doi.org/10.3390/cells10051087
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