ijms-logo

Journal Browser

Journal Browser

Mechanobiology of Organelles

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Biophysics".

Deadline for manuscript submissions: closed (31 July 2021) | Viewed by 3827

Special Issue Editor


E-Mail Website
Guest Editor
Department of Biomedical Engineering, Boston University, Boston, MA, USA
Interests: respiratory and vascular diseases, mechanotransduction pathways; respiratory and vascular mechanobiology; mechanobiology of organelles; protein post-translational modifications and regulations; real time live imaging; vascular tissue engineering

Special Issue Information

Dear Colleagues,

Physiological forces (stretch, pressure, sheer flow, compression, stiffness) due to touch, movement, gravity, blood flow, blood pressure or breathing significantly influence many basic cell functions. This mechanical stimuli-initiated molecular mechanotransduction, the conversion of mechanical forces to molecular signaling, has been intensively studied in a variety of biological systems. It is evident that mechanosignaling plays a fundamental role in the genesis and maintenance of normal structure and function of tissues, and it is involved in diseases such as cardiovascular, respiratory or even metabolic disorders. Mechanotransduction is a complex multiscale process: The extracellular matrix (ECM) network interacts simultaneously with many cells through adhesion receptors such as integrins or catherins at focal adhesion (FA) sites which in turn structurally and functionally regulate the cellular peripheral membrane proteins and their linkage to the cytoskeleton, including actin microfilaments, microtubules, and intermediate filaments. These events involve multimolecular biophysical events, complex biochemical reactions, as well as whole organelle responses such as the reorganization of the cytoskeleton, organelle biogenesis, fission-fusion of the mitochondria or changes in shape and structure with consequences to organelle function.

The membrane bound organelles such as the nucleus, the mitochondria, the Golgi apparatus, the lysosome, and the endoplasmic reticulum are embedded in the jell-o-like cytosol and connected to the non-membrane-bound organelles such as microtubules, actin and intermediate filament networks. These dynamic cytoskeletal structures are connected to the ECM through FAs at the cell membrane, which in turn are exposed to external mechanical stimuli to which the organelles respond. The goal of this Special Issue is to broaden our understanding of how mechanical forces are involved and regulate specific organelle functions.

Dr. Elizabeth Bartolak-Suki
Guest Editor

Manuscript Submission Information

Manuscripts should be submitted online at www.mdpi.com by registering and logging in to this website. Once you are registered, click here to go to the submission form. Manuscripts can be submitted until the deadline. All submissions that pass pre-check are peer-reviewed. Accepted papers will be published continuously in the journal (as soon as accepted) and will be listed together on the special issue website. Research articles, review articles as well as short communications are invited. For planned papers, a title and short abstract (about 100 words) can be sent to the Editorial Office for announcement on this website.

Submitted manuscripts should not have been published previously, nor be under consideration for publication elsewhere (except conference proceedings papers). All manuscripts are thoroughly refereed through a single-blind peer-review process. A guide for authors and other relevant information for submission of manuscripts is available on the Instructions for Authors page. International Journal of Molecular Sciences is an international peer-reviewed open access semimonthly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. There is an Article Processing Charge (APC) for publication in this open access journal. For details about the APC please see here. Submitted papers should be well formatted and use good English. Authors may use MDPI's English editing service prior to publication or during author revisions.

Keywords

  • Organelle
  • Homeostais
  • Fluctuating enviroment
  • Aging
  • Vascular diseases
  • Respiratory diseases
  • Excercise
  • Cell adhesion
  • Structure

Published Papers (1 paper)

Order results
Result details
Select all
Export citation of selected articles as:

Research

16 pages, 3362 KiB  
Article
Polycystin-2 Is Required for Chondrocyte Mechanotransduction and Traffics to the Primary Cilium in Response to Mechanical Stimulation
by Clare L. Thompson, Megan McFie, J. Paul Chapple, Philip Beales and Martin M. Knight
Int. J. Mol. Sci. 2021, 22(9), 4313; https://0-doi-org.brum.beds.ac.uk/10.3390/ijms22094313 - 21 Apr 2021
Cited by 16 | Viewed by 3401
Abstract
Primary cilia and associated intraflagellar transport are essential for skeletal development, joint homeostasis, and the response to mechanical stimuli, although the mechanisms remain unclear. Polycystin-2 (PC2) is a member of the transient receptor potential polycystic (TRPP) family of cation channels, and together with [...] Read more.
Primary cilia and associated intraflagellar transport are essential for skeletal development, joint homeostasis, and the response to mechanical stimuli, although the mechanisms remain unclear. Polycystin-2 (PC2) is a member of the transient receptor potential polycystic (TRPP) family of cation channels, and together with Polycystin-1 (PC1), it has been implicated in cilia-mediated mechanotransduction in epithelial cells. The current study investigates the effect of mechanical stimulation on the localization of ciliary polycystins in chondrocytes and tests the hypothesis that they are required in chondrocyte mechanosignaling. Isolated chondrocytes were subjected to mechanical stimulation in the form of uniaxial cyclic tensile strain (CTS) in order to examine the effects on PC2 ciliary localization and matrix gene expression. In the absence of strain, PC2 localizes to the chondrocyte ciliary membrane and neither PC1 nor PC2 are required for ciliogenesis. Cartilage matrix gene expression (Acan, Col2a) is increased in response to 10% CTS. This response is inhibited by siRNA-mediated loss of PC1 or PC2 expression. PC2 ciliary localization requires PC1 and is increased in response to CTS. Increased PC2 cilia trafficking is dependent on the activation of transient receptor potential cation channel subfamily V member 4 (TRPV4) activation. Together, these findings demonstrate for the first time that polycystins are required for chondrocyte mechanotransduction and highlight the mechanosensitive cilia trafficking of PC2 as an important component of cilia-mediated mechanotransduction. Full article
(This article belongs to the Special Issue Mechanobiology of Organelles)
Show Figures

Figure 1

Back to TopTop