Cargando…
Laminin Levels Regulate Tissue Migration and Anterior-Posterior Polarity during Egg Morphogenesis in Drosophila
Basement membranes (BMs) are specialized extracellular matrices required for tissue organization and organ formation. We study the role of laminin and its integrin receptor in the regulation of tissue migration during Drosophila oogenesis. Egg production in Drosophila involves the collective migrati...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507772/ https://www.ncbi.nlm.nih.gov/pubmed/28683315 http://dx.doi.org/10.1016/j.celrep.2017.06.031 |
_version_ | 1783249775649357824 |
---|---|
author | Díaz de la Loza, María C. Díaz-Torres, Alfonsa Zurita, Federico Rosales-Nieves, Alicia E. Moeendarbary, Emad Franze, Kristian Martín-Bermudo, María D. González-Reyes, Acaimo |
author_facet | Díaz de la Loza, María C. Díaz-Torres, Alfonsa Zurita, Federico Rosales-Nieves, Alicia E. Moeendarbary, Emad Franze, Kristian Martín-Bermudo, María D. González-Reyes, Acaimo |
author_sort | Díaz de la Loza, María C. |
collection | PubMed |
description | Basement membranes (BMs) are specialized extracellular matrices required for tissue organization and organ formation. We study the role of laminin and its integrin receptor in the regulation of tissue migration during Drosophila oogenesis. Egg production in Drosophila involves the collective migration of follicle cells (FCs) over the BM to shape the mature egg. We show that laminin content in the BM increases with time, whereas integrin amounts in FCs do not vary significantly. Manipulation of integrin and laminin levels reveals that a dynamic balance of integrin-laminin amounts determines the onset and speed of FC migration. Thus, the interplay of ligand-receptor levels regulates tissue migration in vivo. Laminin depletion also affects the ultrastructure and biophysical properties of the BM and results in anterior-posterior misorientation of developing follicles. Laminin emerges as a key player in the regulation of collective cell migration, tissue stiffness, and the organization of anterior-posterior polarity in Drosophila. |
format | Online Article Text |
id | pubmed-5507772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-55077722017-07-21 Laminin Levels Regulate Tissue Migration and Anterior-Posterior Polarity during Egg Morphogenesis in Drosophila Díaz de la Loza, María C. Díaz-Torres, Alfonsa Zurita, Federico Rosales-Nieves, Alicia E. Moeendarbary, Emad Franze, Kristian Martín-Bermudo, María D. González-Reyes, Acaimo Cell Rep Article Basement membranes (BMs) are specialized extracellular matrices required for tissue organization and organ formation. We study the role of laminin and its integrin receptor in the regulation of tissue migration during Drosophila oogenesis. Egg production in Drosophila involves the collective migration of follicle cells (FCs) over the BM to shape the mature egg. We show that laminin content in the BM increases with time, whereas integrin amounts in FCs do not vary significantly. Manipulation of integrin and laminin levels reveals that a dynamic balance of integrin-laminin amounts determines the onset and speed of FC migration. Thus, the interplay of ligand-receptor levels regulates tissue migration in vivo. Laminin depletion also affects the ultrastructure and biophysical properties of the BM and results in anterior-posterior misorientation of developing follicles. Laminin emerges as a key player in the regulation of collective cell migration, tissue stiffness, and the organization of anterior-posterior polarity in Drosophila. Cell Press 2017-07-05 /pmc/articles/PMC5507772/ /pubmed/28683315 http://dx.doi.org/10.1016/j.celrep.2017.06.031 Text en © 2017 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Díaz de la Loza, María C. Díaz-Torres, Alfonsa Zurita, Federico Rosales-Nieves, Alicia E. Moeendarbary, Emad Franze, Kristian Martín-Bermudo, María D. González-Reyes, Acaimo Laminin Levels Regulate Tissue Migration and Anterior-Posterior Polarity during Egg Morphogenesis in Drosophila |
title | Laminin Levels Regulate Tissue Migration and Anterior-Posterior Polarity during Egg Morphogenesis in Drosophila |
title_full | Laminin Levels Regulate Tissue Migration and Anterior-Posterior Polarity during Egg Morphogenesis in Drosophila |
title_fullStr | Laminin Levels Regulate Tissue Migration and Anterior-Posterior Polarity during Egg Morphogenesis in Drosophila |
title_full_unstemmed | Laminin Levels Regulate Tissue Migration and Anterior-Posterior Polarity during Egg Morphogenesis in Drosophila |
title_short | Laminin Levels Regulate Tissue Migration and Anterior-Posterior Polarity during Egg Morphogenesis in Drosophila |
title_sort | laminin levels regulate tissue migration and anterior-posterior polarity during egg morphogenesis in drosophila |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507772/ https://www.ncbi.nlm.nih.gov/pubmed/28683315 http://dx.doi.org/10.1016/j.celrep.2017.06.031 |
work_keys_str_mv | AT diazdelalozamariac lamininlevelsregulatetissuemigrationandanteriorposteriorpolarityduringeggmorphogenesisindrosophila AT diaztorresalfonsa lamininlevelsregulatetissuemigrationandanteriorposteriorpolarityduringeggmorphogenesisindrosophila AT zuritafederico lamininlevelsregulatetissuemigrationandanteriorposteriorpolarityduringeggmorphogenesisindrosophila AT rosalesnievesaliciae lamininlevelsregulatetissuemigrationandanteriorposteriorpolarityduringeggmorphogenesisindrosophila AT moeendarbaryemad lamininlevelsregulatetissuemigrationandanteriorposteriorpolarityduringeggmorphogenesisindrosophila AT franzekristian lamininlevelsregulatetissuemigrationandanteriorposteriorpolarityduringeggmorphogenesisindrosophila AT martinbermudomariad lamininlevelsregulatetissuemigrationandanteriorposteriorpolarityduringeggmorphogenesisindrosophila AT gonzalezreyesacaimo lamininlevelsregulatetissuemigrationandanteriorposteriorpolarityduringeggmorphogenesisindrosophila |