Plasma membrane mechanosensing upon stretch-induced topography remodelling

Programa de Doctorat en Biomedicina / Tesi realitzada a l'Institut de Bioenginyeria de Catalunya (IBEC)

Detalles Bibliográficos
Autor: Quiroga Álvarez, Xarxa
Tipo de recurso: tesis doctoral
Estado:Versión publicada
Fecha de publicación:2021
País:España
Institución:CBUC, CESCA
Repositorio:TDR. Tesis Doctorales en Red
OAI Identifier:oai:www.tdx.cat:10803/672367
Acceso en línea:http://hdl.handle.net/10803/672367
Access Level:acceso abierto
Palabra clave:Biologia molecular
Biología molecular
Molecular biology
Membranes cel·lulars
Membranas celulares
Cell membranes
Proteïnes
Proteínas
Proteins
Ciències de la Salut
577
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oai_identifier_str oai:www.tdx.cat:10803/672367
network_acronym_str ES
network_name_str España
repository_id_str
dc.title.none.fl_str_mv Plasma membrane mechanosensing upon stretch-induced topography remodelling
title Plasma membrane mechanosensing upon stretch-induced topography remodelling
spellingShingle Plasma membrane mechanosensing upon stretch-induced topography remodelling
Quiroga Álvarez, Xarxa
Biologia molecular
Biología molecular
Molecular biology
Membranes cel·lulars
Membranas celulares
Cell membranes
Proteïnes
Proteínas
Proteins
Ciències de la Salut
577
title_short Plasma membrane mechanosensing upon stretch-induced topography remodelling
title_full Plasma membrane mechanosensing upon stretch-induced topography remodelling
title_fullStr Plasma membrane mechanosensing upon stretch-induced topography remodelling
title_full_unstemmed Plasma membrane mechanosensing upon stretch-induced topography remodelling
title_sort Plasma membrane mechanosensing upon stretch-induced topography remodelling
dc.creator.none.fl_str_mv Quiroga Álvarez, Xarxa
author Quiroga Álvarez, Xarxa
author_facet Quiroga Álvarez, Xarxa
author_role author
dc.contributor.none.fl_str_mv Roca-Cusachs Soulere, Pere
Roca-Cusach Soulere, Pere
Universitat de Barcelona. Facultat de Medicina i Ciències de la Salut
dc.subject.none.fl_str_mv Biologia molecular
Biología molecular
Molecular biology
Membranes cel·lulars
Membranas celulares
Cell membranes
Proteïnes
Proteínas
Proteins
Ciències de la Salut
577
topic Biologia molecular
Biología molecular
Molecular biology
Membranes cel·lulars
Membranas celulares
Cell membranes
Proteïnes
Proteínas
Proteins
Ciències de la Salut
577
description Programa de Doctorat en Biomedicina / Tesi realitzada a l'Institut de Bioenginyeria de Catalunya (IBEC)
publishDate 2021
dc.date.none.fl_str_mv 2021
2021
2022
dc.type.none.fl_str_mv info:eu-repo/semantics/doctoralThesis
info:eu-repo/semantics/publishedVersion
format doctoralThesis
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/10803/672367
url http://hdl.handle.net/10803/672367
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.rights.none.fl_str_mv http://creativecommons.org/licenses/by-nd/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv http://creativecommons.org/licenses/by-nd/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 137 p.
application/pdf
application/pdf
dc.publisher.none.fl_str_mv Universitat de Barcelona
publisher.none.fl_str_mv Universitat de Barcelona
dc.source.none.fl_str_mv TDX (Tesis Doctorals en Xarxa)
reponame:TDR. Tesis Doctorales en Red
instname:CBUC, CESCA
instname_str CBUC, CESCA
reponame_str TDR. Tesis Doctorales en Red
collection TDR. Tesis Doctorales en Red
repository.name.fl_str_mv
repository.mail.fl_str_mv
_version_ 1869405142452797440
spelling Plasma membrane mechanosensing upon stretch-induced topography remodellingQuiroga Álvarez, XarxaBiologia molecularBiología molecularMolecular biologyMembranes cel·lularsMembranas celularesCell membranesProteïnesProteínasProteinsCiències de la Salut577Programa de Doctorat en Biomedicina / Tesi realitzada a l'Institut de Bioenginyeria de Catalunya (IBEC)Five years ago, I started walking this path that now seems like an entire life. Although everyone around tried to explain how this would feel, none of their explanations could have match what it has been in the end. And this is exactly how living systems are, at all levels. The harder the scientists try to feed our curiosity taking closer looks to them, inspecting the question from a different angle, and despite all the previous knowledge that we could gather; the more they surprise us and reveal new ways of sensing, reacting and adapting to the environment. And I think this is exactly what drove me here. I wanted to understand how this is done. I wanted to “see” it. How is it possible that a cell “understands” what is going on around? Which are the parameters that they sense? Biochemistry alone does not answer the question. In a crowded environment, such as it is our body, cells are exposed to thousands of mechanical stimuli too. And those can be also harnessed and transformed into chemical responses as a way of signalling. While the classical biochemical inputs have long been studied, loads of questions remain open about how cells interpret those physical stimuli around them, and microscopy comes as a powerful technique to try to answer these queries. In that sense, this thesis represents a small approach in trying to unravel how the plasma membrane, the first boundary between the cell and the extracellular media, can receive mechanical stimuli and convert them into biochemical signals amenable for the cell. To try to answer this question, this work starts with an introduction to the structure and physicochemical characteristics of the plasma membrane. An overview of the cortical component of the cytoskeleton, intrinsically interconnected to this structure, is also provided. Next, a summary of the literature available on how the plasma membrane can perceive mechanical stimuli and which are the associated biochemical responses triggered by them is included as well. This part is based on a review article published by my colleague and co-supervisor Dr. Le Roux and myself at Philosophical Transactions B as part of the 2019 issue “Forces in cancer” [1]. After the introduction, chapter 2 describes the objectives of this study, which can be summarised as trying to unravel the way in which cells couple mechanical signals at their plasma membrane to biochemical cascades that mediate a response to those. Following, chapters 3 and 4 compose the main body of this thesis, including the methods and the experimental results coming from this research work. Both sections constitute a scientific article that has been recently submitted for publication. In chapter 3 the simplified model chosen to study the question of how cells sense and integrate mechanical stimuli at their plasma membrane is described. This consisted in submitting fibroblast to a controlled stretch-release cycle, forcing them to quickly adapt their shape, mimmicking a highly-relevant scenario in physiology. Chapter 4 recapitulates the way in which plasma membrane reacted to this mechanical perturbation. In the first place, the structure reacted by passively forming evaginations on the nanometric scale of homogeneous size and shape. These evaginations are next recognised by the I- BAR protein IRSp53, which subsequently organizes a node of actin polymerisation dependent on Rac1 and Arp2/3 that mediates the flattening of the structures. Absence of IRSp53 results, thus, in an impaired recovery of homeostasis after stretch. To reinforce the obtained experimental results, theoretical framework to model the mechanics of the system was generated in collaboration with the group of Dr. Arroyo at the Centre Internacional de Mètodes Numèrics en Enginyeria (CIMNE). The aim of this model was to describe how a network generated by the Arp2/3 complex, until now described to push, is able to generate in-plane forces that mediate the ironing of the evagination. Chapter 5 includes a discussion about the limitations of the technique, the novelty of the presented findings, the possible physiological scenarios where the described mechanochemical pathway can be of relevance and, finally, some exciting and unexplored questions that remained open after this work. Additionally, other scientific production obtained during this thesis consisting in unexplored results or work belonging to other publications, has been added at the end of this manuscript in four appendixes. On the first one, I describe all the efforts made during the first 1 year and a half of the PhD to improve immunostaining technique for plasma membrane bound proteins in order to try to stain endogenous BAR proteins. The second appendix gathers the findings obtained from the silencing assay of BAR candidates likely to recognise the curved shape of the stretch-release generated evaginations. The third appendix contains experimental results part of a different publication from Le Roux et al. now under review in Nature Communications [2]. Here, I studied the response of the N-BAR protein Amphiphysin after mechanical stimulation in cells. A fourth appendix including scanning electron microscopy representative images of stretch-release generated evaginations in other cell lines is also added. Finally, I included two more appendix containing the sequencing of all the IRSp53 plasmids used for the body of the work of this thesis and the MATLAB code used for analysis of evaginations flattening dynamics after stretch.Universitat de BarcelonaRoca-Cusachs Soulere, PereRoca-Cusach Soulere, PereUniversitat de Barcelona. Facultat de Medicina i Ciències de la Salut202120222021info:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/publishedVersion137 p.application/pdfapplication/pdfhttp://hdl.handle.net/10803/672367TDX (Tesis Doctorals en Xarxa)reponame:TDR. Tesis Doctorales en Redinstname:CBUC, CESCAInglésL'accés als continguts d'aquesta tesi queda condicionat a l'acceptació de les condicions d'ús establertes per la següent llicència Creative Commons: http://creativecommons.org/licenses/by-nd/4.0/http://creativecommons.org/licenses/by-nd/4.0/info:eu-repo/semantics/openAccessoai:www.tdx.cat:10803/6723672026-06-14T12:46:07Z
score 15.301603