Cargando…

Hypertensive Stimuli Indirectly Stimulate Lymphangiogenesis through Immune Cell Secreted Factors

(1) Background: Renal immune cells and lymphatic vessel (LV) density have been reported previously to be increased in multiple mouse models of hypertension (HTN). However, whether interstitial levels of HTN stimuli such as angiotensin II, salt, or asymmetric dimethylarginine have a direct or indirec...

Descripción completa

Detalles Bibliográficos
Autores principales: Wilcox, Brooke K., Henley, Marissa R., Navaneethabalakrishnan, Shobana, Martinez, Karina A., Pournouri, Anil, Goodlett, Bethany L., Lopez, Alexandra H., Allbee, Miranda L., Pickup, Emma J., Bayless, Kayla J., Chakraborty, Sanjukta, Mitchell, Brett M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315625/
https://www.ncbi.nlm.nih.gov/pubmed/35883582
http://dx.doi.org/10.3390/cells11142139
_version_ 1784754608365633536
author Wilcox, Brooke K.
Henley, Marissa R.
Navaneethabalakrishnan, Shobana
Martinez, Karina A.
Pournouri, Anil
Goodlett, Bethany L.
Lopez, Alexandra H.
Allbee, Miranda L.
Pickup, Emma J.
Bayless, Kayla J.
Chakraborty, Sanjukta
Mitchell, Brett M.
author_facet Wilcox, Brooke K.
Henley, Marissa R.
Navaneethabalakrishnan, Shobana
Martinez, Karina A.
Pournouri, Anil
Goodlett, Bethany L.
Lopez, Alexandra H.
Allbee, Miranda L.
Pickup, Emma J.
Bayless, Kayla J.
Chakraborty, Sanjukta
Mitchell, Brett M.
author_sort Wilcox, Brooke K.
collection PubMed
description (1) Background: Renal immune cells and lymphatic vessel (LV) density have been reported previously to be increased in multiple mouse models of hypertension (HTN). However, whether interstitial levels of HTN stimuli such as angiotensin II, salt, or asymmetric dimethylarginine have a direct or indirect effect on lymphangiogenesis is unknown. We hypothesized that these 3 HTN stimuli directly increase lymphatic endothelial cell (LEC) proliferation, LEC 3-D matrix invasion and vessel formation, and sprouting of mouse mesometrial LVs. (2) Methods: Human LECs (hLECs) and mouse LECs (mLECs) were treated with HTN stimuli while explanted mouse mesometrial LVs were treated with either the same HTN stimuli or with HTN stimuli-conditioned media. Conditioned media was prepared by treating murine splenocytes with HTN stimuli. (3) Results: HTN stimuli had no direct effect on hLEC or mLEC proliferation. Treatment of hLECs with HTN stimuli increased the number of lumen-forming structures and invasion distance (both p < 0.05) in the 3-D matrix but decreased the average lumen diameter and the number of cells per invading structure (both p < 0.05). Conditioned media from HTN-stimuli-treated splenocytes significantly attenuated the decrease in sprout number (aside from salt) and sprout length of mouse mesometrial LVs that is found in the HTN stimuli alone. (4) Conclusions: These data indicate that HTN stimuli indirectly prevent a decrease in lymphangiogenesis through secreted factors from HTN-stimuli-treated immune cells.
format Online
Article
Text
id pubmed-9315625
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-93156252022-07-27 Hypertensive Stimuli Indirectly Stimulate Lymphangiogenesis through Immune Cell Secreted Factors Wilcox, Brooke K. Henley, Marissa R. Navaneethabalakrishnan, Shobana Martinez, Karina A. Pournouri, Anil Goodlett, Bethany L. Lopez, Alexandra H. Allbee, Miranda L. Pickup, Emma J. Bayless, Kayla J. Chakraborty, Sanjukta Mitchell, Brett M. Cells Article (1) Background: Renal immune cells and lymphatic vessel (LV) density have been reported previously to be increased in multiple mouse models of hypertension (HTN). However, whether interstitial levels of HTN stimuli such as angiotensin II, salt, or asymmetric dimethylarginine have a direct or indirect effect on lymphangiogenesis is unknown. We hypothesized that these 3 HTN stimuli directly increase lymphatic endothelial cell (LEC) proliferation, LEC 3-D matrix invasion and vessel formation, and sprouting of mouse mesometrial LVs. (2) Methods: Human LECs (hLECs) and mouse LECs (mLECs) were treated with HTN stimuli while explanted mouse mesometrial LVs were treated with either the same HTN stimuli or with HTN stimuli-conditioned media. Conditioned media was prepared by treating murine splenocytes with HTN stimuli. (3) Results: HTN stimuli had no direct effect on hLEC or mLEC proliferation. Treatment of hLECs with HTN stimuli increased the number of lumen-forming structures and invasion distance (both p < 0.05) in the 3-D matrix but decreased the average lumen diameter and the number of cells per invading structure (both p < 0.05). Conditioned media from HTN-stimuli-treated splenocytes significantly attenuated the decrease in sprout number (aside from salt) and sprout length of mouse mesometrial LVs that is found in the HTN stimuli alone. (4) Conclusions: These data indicate that HTN stimuli indirectly prevent a decrease in lymphangiogenesis through secreted factors from HTN-stimuli-treated immune cells. MDPI 2022-07-07 /pmc/articles/PMC9315625/ /pubmed/35883582 http://dx.doi.org/10.3390/cells11142139 Text en © 2022 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
Wilcox, Brooke K.
Henley, Marissa R.
Navaneethabalakrishnan, Shobana
Martinez, Karina A.
Pournouri, Anil
Goodlett, Bethany L.
Lopez, Alexandra H.
Allbee, Miranda L.
Pickup, Emma J.
Bayless, Kayla J.
Chakraborty, Sanjukta
Mitchell, Brett M.
Hypertensive Stimuli Indirectly Stimulate Lymphangiogenesis through Immune Cell Secreted Factors
title Hypertensive Stimuli Indirectly Stimulate Lymphangiogenesis through Immune Cell Secreted Factors
title_full Hypertensive Stimuli Indirectly Stimulate Lymphangiogenesis through Immune Cell Secreted Factors
title_fullStr Hypertensive Stimuli Indirectly Stimulate Lymphangiogenesis through Immune Cell Secreted Factors
title_full_unstemmed Hypertensive Stimuli Indirectly Stimulate Lymphangiogenesis through Immune Cell Secreted Factors
title_short Hypertensive Stimuli Indirectly Stimulate Lymphangiogenesis through Immune Cell Secreted Factors
title_sort hypertensive stimuli indirectly stimulate lymphangiogenesis through immune cell secreted factors
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9315625/
https://www.ncbi.nlm.nih.gov/pubmed/35883582
http://dx.doi.org/10.3390/cells11142139
work_keys_str_mv AT wilcoxbrookek hypertensivestimuliindirectlystimulatelymphangiogenesisthroughimmunecellsecretedfactors
AT henleymarissar hypertensivestimuliindirectlystimulatelymphangiogenesisthroughimmunecellsecretedfactors
AT navaneethabalakrishnanshobana hypertensivestimuliindirectlystimulatelymphangiogenesisthroughimmunecellsecretedfactors
AT martinezkarinaa hypertensivestimuliindirectlystimulatelymphangiogenesisthroughimmunecellsecretedfactors
AT pournourianil hypertensivestimuliindirectlystimulatelymphangiogenesisthroughimmunecellsecretedfactors
AT goodlettbethanyl hypertensivestimuliindirectlystimulatelymphangiogenesisthroughimmunecellsecretedfactors
AT lopezalexandrah hypertensivestimuliindirectlystimulatelymphangiogenesisthroughimmunecellsecretedfactors
AT allbeemirandal hypertensivestimuliindirectlystimulatelymphangiogenesisthroughimmunecellsecretedfactors
AT pickupemmaj hypertensivestimuliindirectlystimulatelymphangiogenesisthroughimmunecellsecretedfactors
AT baylesskaylaj hypertensivestimuliindirectlystimulatelymphangiogenesisthroughimmunecellsecretedfactors
AT chakrabortysanjukta hypertensivestimuliindirectlystimulatelymphangiogenesisthroughimmunecellsecretedfactors
AT mitchellbrettm hypertensivestimuliindirectlystimulatelymphangiogenesisthroughimmunecellsecretedfactors