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Delimiting CD34+ Stromal Cells/Telocytes Are Resident Mesenchymal Cells That Participate in Neovessel Formation in Skin Kaposi Sarcoma

Kaposi sarcoma (KS) is an angioproliferative lesion in which two main KS cell sources are currently sustained: endothelial cells (ECs) and mesenchymal/stromal cells. Our objective is to establish the tissue location, characteristics and transdifferentiation steps to the KS cells of the latter. For t...

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Autores principales: Díaz-Flores, Lucio, Gutiérrez, Ricardo, González-Gómez, Miriam, García, Maria del Pino, Palmas, Marta, Carrasco, Jose Luis, Madrid, Juan Francisco
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9962853/
https://www.ncbi.nlm.nih.gov/pubmed/36835203
http://dx.doi.org/10.3390/ijms24043793
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author Díaz-Flores, Lucio
Gutiérrez, Ricardo
González-Gómez, Miriam
García, Maria del Pino
Palmas, Marta
Carrasco, Jose Luis
Madrid, Juan Francisco
Díaz-Flores, Lucio
author_facet Díaz-Flores, Lucio
Gutiérrez, Ricardo
González-Gómez, Miriam
García, Maria del Pino
Palmas, Marta
Carrasco, Jose Luis
Madrid, Juan Francisco
Díaz-Flores, Lucio
author_sort Díaz-Flores, Lucio
collection PubMed
description Kaposi sarcoma (KS) is an angioproliferative lesion in which two main KS cell sources are currently sustained: endothelial cells (ECs) and mesenchymal/stromal cells. Our objective is to establish the tissue location, characteristics and transdifferentiation steps to the KS cells of the latter. For this purpose, we studied specimens of 49 cases of cutaneous KS using immunochemistry and confocal and electron microscopy. The results showed that delimiting CD34+ stromal cells/Telocytes (CD34+SCs/TCs) in the external layer of the pre-existing blood vessels and around skin appendages form small convergent lumens, express markers for ECs of blood and lymphatic vessels, share ultrastructural characteristics with ECs and participate in the origin of two main types of neovessels, the evolution of which gives rise to lymphangiomatous or spindle-cell patterns—the substrate of the main KS histopathological variants. Intraluminal folds and pillars (papillae) are formed in the neovessels, which suggests they increase by vessel splitting (intussusceptive angiogenesis and intussusceptive lymphangiogenesis). In conclusion, delimiting CD34+SCs/TCs are mesenchymal/stromal cells that can transdifferentiate into KS ECs, participating in the formation of two types of neovessels. The subsequent growth of the latter involves intussusceptive mechanisms, originating several KS variants. These findings are of histogenic, clinical and therapeutic interest.
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spelling pubmed-99628532023-02-26 Delimiting CD34+ Stromal Cells/Telocytes Are Resident Mesenchymal Cells That Participate in Neovessel Formation in Skin Kaposi Sarcoma Díaz-Flores, Lucio Gutiérrez, Ricardo González-Gómez, Miriam García, Maria del Pino Palmas, Marta Carrasco, Jose Luis Madrid, Juan Francisco Díaz-Flores, Lucio Int J Mol Sci Article Kaposi sarcoma (KS) is an angioproliferative lesion in which two main KS cell sources are currently sustained: endothelial cells (ECs) and mesenchymal/stromal cells. Our objective is to establish the tissue location, characteristics and transdifferentiation steps to the KS cells of the latter. For this purpose, we studied specimens of 49 cases of cutaneous KS using immunochemistry and confocal and electron microscopy. The results showed that delimiting CD34+ stromal cells/Telocytes (CD34+SCs/TCs) in the external layer of the pre-existing blood vessels and around skin appendages form small convergent lumens, express markers for ECs of blood and lymphatic vessels, share ultrastructural characteristics with ECs and participate in the origin of two main types of neovessels, the evolution of which gives rise to lymphangiomatous or spindle-cell patterns—the substrate of the main KS histopathological variants. Intraluminal folds and pillars (papillae) are formed in the neovessels, which suggests they increase by vessel splitting (intussusceptive angiogenesis and intussusceptive lymphangiogenesis). In conclusion, delimiting CD34+SCs/TCs are mesenchymal/stromal cells that can transdifferentiate into KS ECs, participating in the formation of two types of neovessels. The subsequent growth of the latter involves intussusceptive mechanisms, originating several KS variants. These findings are of histogenic, clinical and therapeutic interest. MDPI 2023-02-14 /pmc/articles/PMC9962853/ /pubmed/36835203 http://dx.doi.org/10.3390/ijms24043793 Text en © 2023 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 Article
Díaz-Flores, Lucio
Gutiérrez, Ricardo
González-Gómez, Miriam
García, Maria del Pino
Palmas, Marta
Carrasco, Jose Luis
Madrid, Juan Francisco
Díaz-Flores, Lucio
Delimiting CD34+ Stromal Cells/Telocytes Are Resident Mesenchymal Cells That Participate in Neovessel Formation in Skin Kaposi Sarcoma
title Delimiting CD34+ Stromal Cells/Telocytes Are Resident Mesenchymal Cells That Participate in Neovessel Formation in Skin Kaposi Sarcoma
title_full Delimiting CD34+ Stromal Cells/Telocytes Are Resident Mesenchymal Cells That Participate in Neovessel Formation in Skin Kaposi Sarcoma
title_fullStr Delimiting CD34+ Stromal Cells/Telocytes Are Resident Mesenchymal Cells That Participate in Neovessel Formation in Skin Kaposi Sarcoma
title_full_unstemmed Delimiting CD34+ Stromal Cells/Telocytes Are Resident Mesenchymal Cells That Participate in Neovessel Formation in Skin Kaposi Sarcoma
title_short Delimiting CD34+ Stromal Cells/Telocytes Are Resident Mesenchymal Cells That Participate in Neovessel Formation in Skin Kaposi Sarcoma
title_sort delimiting cd34+ stromal cells/telocytes are resident mesenchymal cells that participate in neovessel formation in skin kaposi sarcoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9962853/
https://www.ncbi.nlm.nih.gov/pubmed/36835203
http://dx.doi.org/10.3390/ijms24043793
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