Loading…
Cathepsin X-mediated [beta]2 integrin activation results in nanotube outgrowth
Membrane nanotubes were recently described as a new principle of cell-cell communication enabling complex and specific messaging to distant cells. Calcium fluxes, vesicles, and cell-surface components can all traffic between cells connected by nanotubes. Here we report for the first time the mechani...
Saved in:
Published in: | Cellular and molecular life sciences : CMLS 2009-03, Vol.66 (6), p.1126 |
---|---|
Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | |
---|---|
cites | |
container_end_page | |
container_issue | 6 |
container_start_page | 1126 |
container_title | Cellular and molecular life sciences : CMLS |
container_volume | 66 |
creator | Obermajer, N Jevnikar, Z Doljak, B Sadaghiani, A M Bogyo, M Kos, J |
description | Membrane nanotubes were recently described as a new principle of cell-cell communication enabling complex and specific messaging to distant cells. Calcium fluxes, vesicles, and cell-surface components can all traffic between cells connected by nanotubes. Here we report for the first time the mechanism of membrane nanotube formation in T cells through LFA-1 (CD11a/CD18; αLβ2) integrin activation by the cysteine protease cathepsin X. Cathepsin X is shown to induce persistent LFA-1 activation. Cathepsin X-upregulated T cells exhibit increased homotypic aggregation and polarized, migration-associated morphology in 2D and 3D models, respectively. In these cells, extended uropods are frequently formed, which subsequently elongate to nanotubes connecting T lymphocytes. Our results demonstrate that LFA-1 activation with subsequent cytoskeletal reorganization induces signal transmission through a physically connected network of T lymphocytes for better coordination of their action at various stages of the immune response. [PUBLICATION ABSTRACT] |
doi_str_mv | 10.1007/s00018-009-8829-8 |
format | article |
fullrecord | <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_journals_213513724</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1892624031</sourcerecordid><originalsourceid>FETCH-proquest_journals_2135137243</originalsourceid><addsrcrecordid>eNqNissOQTEURRsh8fwAs8a8nPbi1liIkZHBTUSkOKjQ0p7y-zrwASZ77WQtxvoShhKgHEUAkFoAzITWKk-NteRYgZhBKeu_P9WqarJ2jLccT7Satth6buiKz2gdr8QDT9YQnvj2gGR2iltHeAnZmSPZtyHrHQ8Y051idtwZ5ykdkPtEl-A_dO2yxtncI_Z-7LDBcrGZr8Qz-FfCSPubT8FltVeymMiiVOPir-gLL9RE9Q</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>213513724</pqid></control><display><type>article</type><title>Cathepsin X-mediated [beta]2 integrin activation results in nanotube outgrowth</title><source>Open Access: PubMed Central</source><source>Springer Link</source><creator>Obermajer, N ; Jevnikar, Z ; Doljak, B ; Sadaghiani, A M ; Bogyo, M ; Kos, J</creator><creatorcontrib>Obermajer, N ; Jevnikar, Z ; Doljak, B ; Sadaghiani, A M ; Bogyo, M ; Kos, J</creatorcontrib><description>Membrane nanotubes were recently described as a new principle of cell-cell communication enabling complex and specific messaging to distant cells. Calcium fluxes, vesicles, and cell-surface components can all traffic between cells connected by nanotubes. Here we report for the first time the mechanism of membrane nanotube formation in T cells through LFA-1 (CD11a/CD18; αLβ2) integrin activation by the cysteine protease cathepsin X. Cathepsin X is shown to induce persistent LFA-1 activation. Cathepsin X-upregulated T cells exhibit increased homotypic aggregation and polarized, migration-associated morphology in 2D and 3D models, respectively. In these cells, extended uropods are frequently formed, which subsequently elongate to nanotubes connecting T lymphocytes. Our results demonstrate that LFA-1 activation with subsequent cytoskeletal reorganization induces signal transmission through a physically connected network of T lymphocytes for better coordination of their action at various stages of the immune response. [PUBLICATION ABSTRACT]</description><identifier>ISSN: 1420-682X</identifier><identifier>EISSN: 1420-9071</identifier><identifier>DOI: 10.1007/s00018-009-8829-8</identifier><language>eng</language><publisher>Basel: Springer Nature B.V</publisher><subject>Cellular biology ; Enzymes ; Immune response ; Lymphocytes ; Molecular biology ; Nanotechnology ; Nanotubes</subject><ispartof>Cellular and molecular life sciences : CMLS, 2009-03, Vol.66 (6), p.1126</ispartof><rights>Birkhäuser Verlag, Basel 2009</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Obermajer, N</creatorcontrib><creatorcontrib>Jevnikar, Z</creatorcontrib><creatorcontrib>Doljak, B</creatorcontrib><creatorcontrib>Sadaghiani, A M</creatorcontrib><creatorcontrib>Bogyo, M</creatorcontrib><creatorcontrib>Kos, J</creatorcontrib><title>Cathepsin X-mediated [beta]2 integrin activation results in nanotube outgrowth</title><title>Cellular and molecular life sciences : CMLS</title><description>Membrane nanotubes were recently described as a new principle of cell-cell communication enabling complex and specific messaging to distant cells. Calcium fluxes, vesicles, and cell-surface components can all traffic between cells connected by nanotubes. Here we report for the first time the mechanism of membrane nanotube formation in T cells through LFA-1 (CD11a/CD18; αLβ2) integrin activation by the cysteine protease cathepsin X. Cathepsin X is shown to induce persistent LFA-1 activation. Cathepsin X-upregulated T cells exhibit increased homotypic aggregation and polarized, migration-associated morphology in 2D and 3D models, respectively. In these cells, extended uropods are frequently formed, which subsequently elongate to nanotubes connecting T lymphocytes. Our results demonstrate that LFA-1 activation with subsequent cytoskeletal reorganization induces signal transmission through a physically connected network of T lymphocytes for better coordination of their action at various stages of the immune response. [PUBLICATION ABSTRACT]</description><subject>Cellular biology</subject><subject>Enzymes</subject><subject>Immune response</subject><subject>Lymphocytes</subject><subject>Molecular biology</subject><subject>Nanotechnology</subject><subject>Nanotubes</subject><issn>1420-682X</issn><issn>1420-9071</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><recordid>eNqNissOQTEURRsh8fwAs8a8nPbi1liIkZHBTUSkOKjQ0p7y-zrwASZ77WQtxvoShhKgHEUAkFoAzITWKk-NteRYgZhBKeu_P9WqarJ2jLccT7Satth6buiKz2gdr8QDT9YQnvj2gGR2iltHeAnZmSPZtyHrHQ8Y051idtwZ5ykdkPtEl-A_dO2yxtncI_Z-7LDBcrGZr8Qz-FfCSPubT8FltVeymMiiVOPir-gLL9RE9Q</recordid><startdate>20090301</startdate><enddate>20090301</enddate><creator>Obermajer, N</creator><creator>Jevnikar, Z</creator><creator>Doljak, B</creator><creator>Sadaghiani, A M</creator><creator>Bogyo, M</creator><creator>Kos, J</creator><general>Springer Nature B.V</general><scope>3V.</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SS</scope><scope>7T5</scope><scope>7T7</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U7</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>C1K</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0K</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M7N</scope><scope>M7P</scope><scope>MBDVC</scope><scope>P64</scope><scope>PATMY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>RC3</scope></search><sort><creationdate>20090301</creationdate><title>Cathepsin X-mediated [beta]2 integrin activation results in nanotube outgrowth</title><author>Obermajer, N ; Jevnikar, Z ; Doljak, B ; Sadaghiani, A M ; Bogyo, M ; Kos, J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_journals_2135137243</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Cellular biology</topic><topic>Enzymes</topic><topic>Immune response</topic><topic>Lymphocytes</topic><topic>Molecular biology</topic><topic>Nanotechnology</topic><topic>Nanotubes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Obermajer, N</creatorcontrib><creatorcontrib>Jevnikar, Z</creatorcontrib><creatorcontrib>Doljak, B</creatorcontrib><creatorcontrib>Sadaghiani, A M</creatorcontrib><creatorcontrib>Bogyo, M</creatorcontrib><creatorcontrib>Kos, J</creatorcontrib><collection>ProQuest Central (Corporate)</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Agricultural Science Collection</collection><collection>ProQuest Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Biology Database (Alumni Edition)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Agricultural & Environmental Science Collection</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Agriculture Science Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>ProQuest research library</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Research Library (Corporate)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Environmental Science Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>Environmental Science Collection</collection><collection>ProQuest Central Basic</collection><collection>Genetics Abstracts</collection><jtitle>Cellular and molecular life sciences : CMLS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Obermajer, N</au><au>Jevnikar, Z</au><au>Doljak, B</au><au>Sadaghiani, A M</au><au>Bogyo, M</au><au>Kos, J</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cathepsin X-mediated [beta]2 integrin activation results in nanotube outgrowth</atitle><jtitle>Cellular and molecular life sciences : CMLS</jtitle><date>2009-03-01</date><risdate>2009</risdate><volume>66</volume><issue>6</issue><spage>1126</spage><pages>1126-</pages><issn>1420-682X</issn><eissn>1420-9071</eissn><abstract>Membrane nanotubes were recently described as a new principle of cell-cell communication enabling complex and specific messaging to distant cells. Calcium fluxes, vesicles, and cell-surface components can all traffic between cells connected by nanotubes. Here we report for the first time the mechanism of membrane nanotube formation in T cells through LFA-1 (CD11a/CD18; αLβ2) integrin activation by the cysteine protease cathepsin X. Cathepsin X is shown to induce persistent LFA-1 activation. Cathepsin X-upregulated T cells exhibit increased homotypic aggregation and polarized, migration-associated morphology in 2D and 3D models, respectively. In these cells, extended uropods are frequently formed, which subsequently elongate to nanotubes connecting T lymphocytes. Our results demonstrate that LFA-1 activation with subsequent cytoskeletal reorganization induces signal transmission through a physically connected network of T lymphocytes for better coordination of their action at various stages of the immune response. [PUBLICATION ABSTRACT]</abstract><cop>Basel</cop><pub>Springer Nature B.V</pub><doi>10.1007/s00018-009-8829-8</doi></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1420-682X |
ispartof | Cellular and molecular life sciences : CMLS, 2009-03, Vol.66 (6), p.1126 |
issn | 1420-682X 1420-9071 |
language | eng |
recordid | cdi_proquest_journals_213513724 |
source | Open Access: PubMed Central; Springer Link |
subjects | Cellular biology Enzymes Immune response Lymphocytes Molecular biology Nanotechnology Nanotubes |
title | Cathepsin X-mediated [beta]2 integrin activation results in nanotube outgrowth |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T04%3A17%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Cathepsin%20X-mediated%20%5Bbeta%5D2%20integrin%20activation%20results%20in%20nanotube%20outgrowth&rft.jtitle=Cellular%20and%20molecular%20life%20sciences%20:%20CMLS&rft.au=Obermajer,%20N&rft.date=2009-03-01&rft.volume=66&rft.issue=6&rft.spage=1126&rft.pages=1126-&rft.issn=1420-682X&rft.eissn=1420-9071&rft_id=info:doi/10.1007/s00018-009-8829-8&rft_dat=%3Cproquest%3E1892624031%3C/proquest%3E%3Cgrp_id%3Ecdi_FETCH-proquest_journals_2135137243%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=213513724&rft_id=info:pmid/&rfr_iscdi=true |