Cargando…
Endogenous AJAP1 associates with the cytoskeleton and attenuates angiogenesis in endothelial cells
The adherens junction associated protein 1 (AJAP1, aka shrew-1) is presumably a type-I transmembrane protein localizing and interacting with the E-cadherin-catenin complex. In various tumors, AJAP1 expression is reduced or lost, including hepatocellular and esophageal squamous cell carcinoma, and gl...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Company of Biologists Ltd
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5483013/ https://www.ncbi.nlm.nih.gov/pubmed/28483980 http://dx.doi.org/10.1242/bio.022335 |
_version_ | 1783245675791646720 |
---|---|
author | Hötte, Katharina Smyrek, Isabell Starzinski-Powitz, Anna Stelzer, Ernst H. K. |
author_facet | Hötte, Katharina Smyrek, Isabell Starzinski-Powitz, Anna Stelzer, Ernst H. K. |
author_sort | Hötte, Katharina |
collection | PubMed |
description | The adherens junction associated protein 1 (AJAP1, aka shrew-1) is presumably a type-I transmembrane protein localizing and interacting with the E-cadherin-catenin complex. In various tumors, AJAP1 expression is reduced or lost, including hepatocellular and esophageal squamous cell carcinoma, and glial-derived tumors. The aberrant expression of AJAP1 is associated with alterations in cell migration, invasion, increased tumor growth, and tumor vascularization, suggesting AJAP1 as a putative tumor suppressor. We show that AJAP1 attenuates sprouting angiogenesis by reducing endothelial migration and invasion capacities. Further, we show for the first time that endogenous AJAP1 is associated with the microtubule cytoskeleton. This linkage is independent from cell confluency and stable during angiogenic sprouting in vitro. Our work suggests that AJAP1 is a putative negative regulator of angiogenesis, reducing cell migration and invasion by interfering with the microtubule network. Based on our results and those of other authors, we suggest AJAP1 as a novel tumor suppressor and diagnostic marker. |
format | Online Article Text |
id | pubmed-5483013 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The Company of Biologists Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-54830132017-06-28 Endogenous AJAP1 associates with the cytoskeleton and attenuates angiogenesis in endothelial cells Hötte, Katharina Smyrek, Isabell Starzinski-Powitz, Anna Stelzer, Ernst H. K. Biol Open Research Article The adherens junction associated protein 1 (AJAP1, aka shrew-1) is presumably a type-I transmembrane protein localizing and interacting with the E-cadherin-catenin complex. In various tumors, AJAP1 expression is reduced or lost, including hepatocellular and esophageal squamous cell carcinoma, and glial-derived tumors. The aberrant expression of AJAP1 is associated with alterations in cell migration, invasion, increased tumor growth, and tumor vascularization, suggesting AJAP1 as a putative tumor suppressor. We show that AJAP1 attenuates sprouting angiogenesis by reducing endothelial migration and invasion capacities. Further, we show for the first time that endogenous AJAP1 is associated with the microtubule cytoskeleton. This linkage is independent from cell confluency and stable during angiogenic sprouting in vitro. Our work suggests that AJAP1 is a putative negative regulator of angiogenesis, reducing cell migration and invasion by interfering with the microtubule network. Based on our results and those of other authors, we suggest AJAP1 as a novel tumor suppressor and diagnostic marker. The Company of Biologists Ltd 2017-05-08 /pmc/articles/PMC5483013/ /pubmed/28483980 http://dx.doi.org/10.1242/bio.022335 Text en © 2017. Published by The Company of Biologists Ltd http://creativecommons.org/licenses/by/3.0This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed. |
spellingShingle | Research Article Hötte, Katharina Smyrek, Isabell Starzinski-Powitz, Anna Stelzer, Ernst H. K. Endogenous AJAP1 associates with the cytoskeleton and attenuates angiogenesis in endothelial cells |
title | Endogenous AJAP1 associates with the cytoskeleton and attenuates angiogenesis in endothelial cells |
title_full | Endogenous AJAP1 associates with the cytoskeleton and attenuates angiogenesis in endothelial cells |
title_fullStr | Endogenous AJAP1 associates with the cytoskeleton and attenuates angiogenesis in endothelial cells |
title_full_unstemmed | Endogenous AJAP1 associates with the cytoskeleton and attenuates angiogenesis in endothelial cells |
title_short | Endogenous AJAP1 associates with the cytoskeleton and attenuates angiogenesis in endothelial cells |
title_sort | endogenous ajap1 associates with the cytoskeleton and attenuates angiogenesis in endothelial cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5483013/ https://www.ncbi.nlm.nih.gov/pubmed/28483980 http://dx.doi.org/10.1242/bio.022335 |
work_keys_str_mv | AT hottekatharina endogenousajap1associateswiththecytoskeletonandattenuatesangiogenesisinendothelialcells AT smyrekisabell endogenousajap1associateswiththecytoskeletonandattenuatesangiogenesisinendothelialcells AT starzinskipowitzanna endogenousajap1associateswiththecytoskeletonandattenuatesangiogenesisinendothelialcells AT stelzerernsthk endogenousajap1associateswiththecytoskeletonandattenuatesangiogenesisinendothelialcells |