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Lysophosphatidic acid does not cause blood/lymphatic vessel plasticity in the rat mesentery culture model

Understanding the mechanisms behind endothelial cell identity is crucial for the goal of manipulating microvascular networks. Lysophosphatidic acid (LPA) and serum stimulation have been suggested to induce a lymphatic identity in blood endothelial cells in vitro. The objective of this study was to d...

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Autores principales: Sweat, Richard S., Azimi, Mohammad S., Suarez‐Martinez, Ariana D., Katakam, Prasad, Murfee, Walter L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4945839/
https://www.ncbi.nlm.nih.gov/pubmed/27401461
http://dx.doi.org/10.14814/phy2.12857
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author Sweat, Richard S.
Azimi, Mohammad S.
Suarez‐Martinez, Ariana D.
Katakam, Prasad
Murfee, Walter L.
author_facet Sweat, Richard S.
Azimi, Mohammad S.
Suarez‐Martinez, Ariana D.
Katakam, Prasad
Murfee, Walter L.
author_sort Sweat, Richard S.
collection PubMed
description Understanding the mechanisms behind endothelial cell identity is crucial for the goal of manipulating microvascular networks. Lysophosphatidic acid (LPA) and serum stimulation have been suggested to induce a lymphatic identity in blood endothelial cells in vitro. The objective of this study was to determine if LPA or serum induces blood‐to‐lymphatic vessel phenotypic transition in microvascular networks. The rat mesentery culture model was used to observe the effect of stimulation on blood and lymphatic microvascular networks ex vivo. Vascularized mesenteric tissues were harvested from adult Wistar rats and cultured with LPA or 10% serum for up to 5 days. Tissues were then immunolabeled with PECAM to identify blood vessels and LYVE‐1 or Prox1 to identify lymphatic vessels. We show that while LPA caused capillary sprouting and increased vascular length density in adult microvascular networks, LPA did not cause a blood‐to‐lymphatic phenotypic transition. The results suggest that LPA is not sufficient to cause blood endothelial cells to adopt a lymphatic identity in adult microvascular networks. Similarly, serum stimulation caused robust angiogenesis and increased lymphatic/blood vessel connections, yet did not induce a blood‐to‐lymphatic phenotypic transition. Our study highlights an understudied area of lymphatic research and warrants future investigation into the mechanisms responsible for the maintenance of blood and lymphatic vessel identity.
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spelling pubmed-49458392016-07-26 Lysophosphatidic acid does not cause blood/lymphatic vessel plasticity in the rat mesentery culture model Sweat, Richard S. Azimi, Mohammad S. Suarez‐Martinez, Ariana D. Katakam, Prasad Murfee, Walter L. Physiol Rep Original Research Understanding the mechanisms behind endothelial cell identity is crucial for the goal of manipulating microvascular networks. Lysophosphatidic acid (LPA) and serum stimulation have been suggested to induce a lymphatic identity in blood endothelial cells in vitro. The objective of this study was to determine if LPA or serum induces blood‐to‐lymphatic vessel phenotypic transition in microvascular networks. The rat mesentery culture model was used to observe the effect of stimulation on blood and lymphatic microvascular networks ex vivo. Vascularized mesenteric tissues were harvested from adult Wistar rats and cultured with LPA or 10% serum for up to 5 days. Tissues were then immunolabeled with PECAM to identify blood vessels and LYVE‐1 or Prox1 to identify lymphatic vessels. We show that while LPA caused capillary sprouting and increased vascular length density in adult microvascular networks, LPA did not cause a blood‐to‐lymphatic phenotypic transition. The results suggest that LPA is not sufficient to cause blood endothelial cells to adopt a lymphatic identity in adult microvascular networks. Similarly, serum stimulation caused robust angiogenesis and increased lymphatic/blood vessel connections, yet did not induce a blood‐to‐lymphatic phenotypic transition. Our study highlights an understudied area of lymphatic research and warrants future investigation into the mechanisms responsible for the maintenance of blood and lymphatic vessel identity. John Wiley and Sons Inc. 2016-07-08 /pmc/articles/PMC4945839/ /pubmed/27401461 http://dx.doi.org/10.14814/phy2.12857 Text en © 2016 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Sweat, Richard S.
Azimi, Mohammad S.
Suarez‐Martinez, Ariana D.
Katakam, Prasad
Murfee, Walter L.
Lysophosphatidic acid does not cause blood/lymphatic vessel plasticity in the rat mesentery culture model
title Lysophosphatidic acid does not cause blood/lymphatic vessel plasticity in the rat mesentery culture model
title_full Lysophosphatidic acid does not cause blood/lymphatic vessel plasticity in the rat mesentery culture model
title_fullStr Lysophosphatidic acid does not cause blood/lymphatic vessel plasticity in the rat mesentery culture model
title_full_unstemmed Lysophosphatidic acid does not cause blood/lymphatic vessel plasticity in the rat mesentery culture model
title_short Lysophosphatidic acid does not cause blood/lymphatic vessel plasticity in the rat mesentery culture model
title_sort lysophosphatidic acid does not cause blood/lymphatic vessel plasticity in the rat mesentery culture model
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4945839/
https://www.ncbi.nlm.nih.gov/pubmed/27401461
http://dx.doi.org/10.14814/phy2.12857
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