Cargando…

Nanotube Action between Human Mesothelial Cells Reveals Novel Aspects of Inflammatory Responses

A well-known role of human peritoneal mesothelial cells (HPMCs), the resident cells of the peritoneal cavity, is the generation of an immune response during peritonitis by activation of T-cells via antigen presentation. Recent findings have shown that intercellular nanotubes (NTs) mediate functional...

Descripción completa

Detalles Bibliográficos
Autores principales: Ranzinger, Julia, Rustom, Amin, Abel, Marcus, Leyh, Julia, Kihm, Lars, Witkowski, Margarete, Scheurich, Peter, Zeier, Martin, Schwenger, Vedat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3246504/
https://www.ncbi.nlm.nih.gov/pubmed/22216308
http://dx.doi.org/10.1371/journal.pone.0029537
_version_ 1782219959066165248
author Ranzinger, Julia
Rustom, Amin
Abel, Marcus
Leyh, Julia
Kihm, Lars
Witkowski, Margarete
Scheurich, Peter
Zeier, Martin
Schwenger, Vedat
author_facet Ranzinger, Julia
Rustom, Amin
Abel, Marcus
Leyh, Julia
Kihm, Lars
Witkowski, Margarete
Scheurich, Peter
Zeier, Martin
Schwenger, Vedat
author_sort Ranzinger, Julia
collection PubMed
description A well-known role of human peritoneal mesothelial cells (HPMCs), the resident cells of the peritoneal cavity, is the generation of an immune response during peritonitis by activation of T-cells via antigen presentation. Recent findings have shown that intercellular nanotubes (NTs) mediate functional connectivity between various cell types including immune cells - such as T-cells, natural killer (NK) cells or macrophages - by facilitating a spectrum of long range cell-cell interactions. Although of medical interest, the relevance of NT-related findings for human medical conditions and treatment, e.g. in relation to inflammatory processes, remains elusive, particularly due to a lack of appropriate in vivo data. Here, we show for the first time that primary cultures of patient derived HPMCs are functionally connected via membranous nanotubes. NT formation appears to be actin cytoskeleton dependent, mediated by the action of filopodia. Importantly, significant variances in NT numbers between different donors as a consequence of pathophysiological alterations were observable. Furthermore, we show that TNF-α induces nanotube formation and demonstrate a strong correlation of NT connectivity in accordance with the cellular cholesterol level and distribution, pointing to a complex involvement of NTs in inflammatory processes with potential impact for clinical treatment.
format Online
Article
Text
id pubmed-3246504
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-32465042012-01-03 Nanotube Action between Human Mesothelial Cells Reveals Novel Aspects of Inflammatory Responses Ranzinger, Julia Rustom, Amin Abel, Marcus Leyh, Julia Kihm, Lars Witkowski, Margarete Scheurich, Peter Zeier, Martin Schwenger, Vedat PLoS One Research Article A well-known role of human peritoneal mesothelial cells (HPMCs), the resident cells of the peritoneal cavity, is the generation of an immune response during peritonitis by activation of T-cells via antigen presentation. Recent findings have shown that intercellular nanotubes (NTs) mediate functional connectivity between various cell types including immune cells - such as T-cells, natural killer (NK) cells or macrophages - by facilitating a spectrum of long range cell-cell interactions. Although of medical interest, the relevance of NT-related findings for human medical conditions and treatment, e.g. in relation to inflammatory processes, remains elusive, particularly due to a lack of appropriate in vivo data. Here, we show for the first time that primary cultures of patient derived HPMCs are functionally connected via membranous nanotubes. NT formation appears to be actin cytoskeleton dependent, mediated by the action of filopodia. Importantly, significant variances in NT numbers between different donors as a consequence of pathophysiological alterations were observable. Furthermore, we show that TNF-α induces nanotube formation and demonstrate a strong correlation of NT connectivity in accordance with the cellular cholesterol level and distribution, pointing to a complex involvement of NTs in inflammatory processes with potential impact for clinical treatment. Public Library of Science 2011-12-27 /pmc/articles/PMC3246504/ /pubmed/22216308 http://dx.doi.org/10.1371/journal.pone.0029537 Text en Ranzinger et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ranzinger, Julia
Rustom, Amin
Abel, Marcus
Leyh, Julia
Kihm, Lars
Witkowski, Margarete
Scheurich, Peter
Zeier, Martin
Schwenger, Vedat
Nanotube Action between Human Mesothelial Cells Reveals Novel Aspects of Inflammatory Responses
title Nanotube Action between Human Mesothelial Cells Reveals Novel Aspects of Inflammatory Responses
title_full Nanotube Action between Human Mesothelial Cells Reveals Novel Aspects of Inflammatory Responses
title_fullStr Nanotube Action between Human Mesothelial Cells Reveals Novel Aspects of Inflammatory Responses
title_full_unstemmed Nanotube Action between Human Mesothelial Cells Reveals Novel Aspects of Inflammatory Responses
title_short Nanotube Action between Human Mesothelial Cells Reveals Novel Aspects of Inflammatory Responses
title_sort nanotube action between human mesothelial cells reveals novel aspects of inflammatory responses
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3246504/
https://www.ncbi.nlm.nih.gov/pubmed/22216308
http://dx.doi.org/10.1371/journal.pone.0029537
work_keys_str_mv AT ranzingerjulia nanotubeactionbetweenhumanmesothelialcellsrevealsnovelaspectsofinflammatoryresponses
AT rustomamin nanotubeactionbetweenhumanmesothelialcellsrevealsnovelaspectsofinflammatoryresponses
AT abelmarcus nanotubeactionbetweenhumanmesothelialcellsrevealsnovelaspectsofinflammatoryresponses
AT leyhjulia nanotubeactionbetweenhumanmesothelialcellsrevealsnovelaspectsofinflammatoryresponses
AT kihmlars nanotubeactionbetweenhumanmesothelialcellsrevealsnovelaspectsofinflammatoryresponses
AT witkowskimargarete nanotubeactionbetweenhumanmesothelialcellsrevealsnovelaspectsofinflammatoryresponses
AT scheurichpeter nanotubeactionbetweenhumanmesothelialcellsrevealsnovelaspectsofinflammatoryresponses
AT zeiermartin nanotubeactionbetweenhumanmesothelialcellsrevealsnovelaspectsofinflammatoryresponses
AT schwengervedat nanotubeactionbetweenhumanmesothelialcellsrevealsnovelaspectsofinflammatoryresponses