Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
4.2
2.6
Journals
JFMK
Special Issues
Selected Papers from TERMIS European Chapter Meeting 2017 on “Biomechanics,...
share announcement

Selected Papers from TERMIS European Chapter Meeting 2017 on “Biomechanics, Morphology and Imaging”

A special issue of Journal of Functional Morphology and Kinesiology (ISSN 2411-5142).

Deadline for manuscript submissions: closed (31 October 2017) | Viewed by 24731

Special Issue Editors

Prof. Dr. Mauro Alini

E-Mail Website
Guest Editor
Musculoskeletal Regeneration Program, AO Research Institute Davos, Clavadelerstrasse 8, 7270 Davos, Switzerland
Interests: cartilage; intervertebral disc; angiogenesis; bone; bioreactor; stem cell; tissue regeneration
Prof. Dr. Martin J Stoddart

E-Mail Website
Guest Editor
Musculoskeletal Regeneration Program, AO Research Institute Davos, Clavadelerstrasse 8, 7270 Davos, Switzerland
Interests: mesenchymal stem cells; chondrogenesis; ostoegenesis; mechanobiology; gene therapy; bone; cartilage
Dr. Victoria Workman

E-Mail Website
Guest Editor
Manchester Institute of Biotechnology, University of Manchester, Manchester, UK
Interests: regenerative medicine; 3D cell culture; bio-electrospraying; biological models; cell encapsulation; cellular kinetics
Prof. Dr. Katja Schenke-Layland

E-Mail Website
Guest Editor
1. Department of Women’s Health, Research Institute for Women’s Health, Eberhard Karls University, Tuebingen, Germany
2. Fraunhofer IGB Stuttgart, Stuttgart, Germany
Interests: regenerative medicine; tissue engineering; cardiovascular development; biomaterials; women's health

Special Issue Information

Dear Colleagues,

The TERMIS European Chapter Meeting 2017 (TERMIS-EU 2017) will be held in Davos, Switzerland, 26–30 June, 2017. More information about the conference can be found at https://www.termis.org/eu2017/.

Participants of the conference are cordially invited to contribute original research papers or reviews to this Special Issue of JFMK. This Special Issue welcomes submission of previously unpublished manuscripts from original work on all aspects of tissue engineering and regenerative medicine focused the main attention on biomechanics, morphology and imaging.

Prof. Dr. Mauro Alini
Prof. Dr. Martin J Stoddart
Dr. Victoria Workman
Prof. Dr. Katja Schenke-Layland
Guest Editors

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. Journal of Functional Morphology and Kinesiology is an international peer-reviewed open access quarterly journal published by MDPI.

Please visit the Instructions for Authors page before submitting a manuscript. The Article Processing Charge (APC) for publication in this open access journal is 1600 CHF (Swiss Francs). 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

  • biomechanics

  • morphology

  • imaging

Benefits of Publishing in a Special Issue

  • Ease of navigation: Grouping papers by topic helps scholars navigate broad scope journals more efficiently.
  • Greater discoverability: Special Issues support the reach and impact of scientific research. Articles in Special Issues are more discoverable and cited more frequently.
  • Expansion of research network: Special Issues facilitate connections among authors, fostering scientific collaborations.
  • External promotion: Articles in Special Issues are often promoted through the journal's social media, increasing their visibility.
  • e-Book format: Special Issues with more than 10 articles can be published as dedicated e-books, ensuring wide and rapid dissemination.

Further information on MDPI's Special Issue polices can be found here.

Published Papers (5 papers)

Download All Papers
Order results
Result details
Show export options expand_more Show export options expand_less
Select all
Export citation of selected articles as:

Research

Jump to: Review

16 pages, 6326 KiB  
Article
Osteoclast Formation within a Human Co-Culture System on Bone Material as an In Vitro Model for Bone Remodeling Processes
by Franziska V. Schmid, Claudia Kleinhans, Freia F. Schmid and Petra J. Kluger
J. Funct. Morphol. Kinesiol. 2018, 3(1), 17; https://doi.org/10.3390/jfmk3010017 - 18 Mar 2018
Cited by 6 | Viewed by 6302
Abstract
Bone remodeling can be mimicked in vitro by co-culture models. Based on bone cells, such co-cultures help to study synergistic morphological changes and the impact of materials and applied substances. Hence, we examined the formation of osteoclasts on bovine bone materials to prove [...] Read more.
Bone remodeling can be mimicked in vitro by co-culture models. Based on bone cells, such co-cultures help to study synergistic morphological changes and the impact of materials and applied substances. Hence, we examined the formation of osteoclasts on bovine bone materials to prove the bone resorption functionality of the osteoclasts in three different co-culture set-ups using human monocytes (hMCs) and (I) human mesenchymal stem cells (hMSCs), (II) osteogenic differentiated hMSCs (hOBs), and (III) hOBs in addition of soluble monocyte-colony stimulating factor (M-CSF) and cytokine receptor activator of NFκB ligand (RANKL). We detected osteoclast-specific actin morphology, as well as the expression of cathepsin K and CD51/61 in single cells in set-up II and in numerous cells in set-up III. Resorption pits on bone material as characteristic proof of functional osteoclasts were not found in set-up I and II, but we detected such resorption pits in set–up III. We conclude in co-culture models without M-CSF and RANKL that monocytes can differentiate into osteoclasts that show the characteristic actin structures and protein expression. However, to receive functional bone resorbing osteoclasts in vitro, the addition of M-CSF and RANKL is needed. Moreover, we suggest the use of bone or bone-like materials for future studies evaluating osteoclastogenesis. Full article
(This article belongs to the Special Issue Selected Papers from TERMIS European Chapter Meeting 2017 on “Biomechanics, Morphology and Imaging”)
►▼ Show Figures

Figure 1

205 KiB  
Article
The Influence of Applied Blood Flow Restriction Cuffs on Kinematics of Submaximal Sprinting
by Ryu Nagahara and Takashi Abe
J. Funct. Morphol. Kinesiol. 2017, 2(4), 45; https://doi.org/10.3390/jfmk2040045 - 5 Dec 2017
Cited by 2 | Viewed by 3504
Abstract
It is unknown how sports activity combined with blood flow restriction (BFR) on the limbs can impact the exercising limb’s motion. We aimed to compare the lower limb kinematics between submaximal sprinting with and without BFR cuffs (i.e., BFR and normal conditions) when [...] Read more.
It is unknown how sports activity combined with blood flow restriction (BFR) on the limbs can impact the exercising limb’s motion. We aimed to compare the lower limb kinematics between submaximal sprinting with and without BFR cuffs (i.e., BFR and normal conditions) when they were applied on the upper thigh. Ten collegiate sprinters performed five 45-m submaximal sprint trials under normal and BFR conditions. The BFR was applied to both legs at the proximal portion of the thigh utilizing elastic cuffs. The cuff pressure was set at approximately 60% of estimated arterial occlusion pressure. Spatiotemporal and hip and knee joint kinematic variables for both legs during submaximal sprinting were obtained using a motion capture system. The results showed, for spatiotemporal variables, no significant difference (p > 0.653), a trivial or small effect size (0.050–0.205), and high correlation coefficients (r > 0.923) between conditions. Moreover, for the joint angles and angular velocities, no significant difference (p > 0.244) and a trivial or small effect size (0.003–0.538), as well as significant correlations (r >0.684) were found between conditions. These results indicate that, in general, there is probably no influence of BFR cuffs on the upper thigh on running kinematics. Full article
(This article belongs to the Special Issue Selected Papers from TERMIS European Chapter Meeting 2017 on “Biomechanics, Morphology and Imaging”)
6986 KiB  
Article
Image-Based Histological Evaluation of Scaffold-Free 3D Osteoblast Cultures
by Sebastian Eggert, Jutta Tuebel, Peter Foehr, Lara Kuntz, Andreas Obermeier, Carmen Marthen, Christian U. Grosse and Rainer Burgkart
J. Funct. Morphol. Kinesiol. 2017, 2(4), 42; https://doi.org/10.3390/jfmk2040042 - 24 Nov 2017
Cited by 2 | Viewed by 4776
Abstract
The analysis of tissue network characteristics and cell distribution using histological methods is widely used. However, image analysis still relies on manual evaluation methods, known as semi-quantitative analysis, which are time-consuming and to a certain degree user-specific. For this reason, automated imaging processing [...] Read more.
The analysis of tissue network characteristics and cell distribution using histological methods is widely used. However, image analysis still relies on manual evaluation methods, known as semi-quantitative analysis, which are time-consuming and to a certain degree user-specific. For this reason, automated imaging processing methods have an enormous potential to increase sample processing and reduce the variation that is caused by a user-specific evaluation. This work demonstrates the feasibility of using a semi-automated image analysis process based on the open source software framework ImageJ and the plug-in Angiogenesis Analyzer to evaluate the quantitative degree of tissue damage within 3D cell constructs after mechanical loading. Within a proof-of-concept study, the semi-automated approach was applied to calculate the Node-to-Free Ratio (N/F-Ratio) and perform a strut analysis for histological evaluation of mechanically compressed samples of human osteoblast-derived 3D constructs. The N/F-Ratio revealed a median value of 1.29 for the control, whereas the values for the mechanically compressed samples decreased to 0.97 for 20% compression, 0.85 for 40%, and 0.86 for 60%. The strut analysis indicated a decrease of the connected branches with increasing compression rate. The newly developed and time-saving processing workflow was successfully established and can be carried out using available, open source software solutions. Full article
(This article belongs to the Special Issue Selected Papers from TERMIS European Chapter Meeting 2017 on “Biomechanics, Morphology and Imaging”)
►▼ Show Figures

Graphical abstract

1684 KiB  
Article
TGF-β1-Dependent Downregulation of HDAC9 Inhibits Maturation of Human Osteoblasts
by Sabrina Ehnert, Elisabeth Heuberger, Caren Linnemann, Andreas K. Nussler and Stefan Pscherer
J. Funct. Morphol. Kinesiol. 2017, 2(4), 41; https://doi.org/10.3390/jfmk2040041 - 13 Nov 2017
Cited by 4 | Viewed by 3513
Abstract
Transforming growth factor β (TGF-β) is a key regulator of bone density. Recently, we have shown that TGF-β1 effectively blocks bone morphogenetic protein-induced maturation of human osteoblasts (hOBs) in a histone deacetylase (HDAC)-dependent manner. To better understand the underlying mechanisms and to [...] Read more.
Transforming growth factor β (TGF-β) is a key regulator of bone density. Recently, we have shown that TGF-β1 effectively blocks bone morphogenetic protein-induced maturation of human osteoblasts (hOBs) in a histone deacetylase (HDAC)-dependent manner. To better understand the underlying mechanisms and to identify possible therapeutic targets, the current study aimed at characterizing the expression changes of different HDACs in hOBs following recombinant human TGF-β1 treatment and investigating the effect of the altered HDACs on both the proliferation and maturation of hOBs and osteogenic cell lines. As expected from our previous work, exposure to rhTGF-β1 induced the expression of HDACs (HDAC1, -2, -3, -6). However, to our surprise, rhTGF-β1 treatment strongly suppressed the expression of HDAC9 during osteogenic differentiation. HDAC9 is reported to suppress osteoclastogenesis; however, little is known about the role of HDAC9 in osteogenesis. Chemical inhibition of HDAC9 with TMP269 increased cell numbers of hOBs, but significantly decreased their osteogenic function (alkaline phosphatase activity and matrix mineralization). In osteogenic cell lines (MG-63, CAL-72 and SAOS-2), the expression of HDAC9 negatively correlates with their proliferation capacity and positively correlates with their osteogenic differentiation potential. Being able to boost osteoclasts while inhibiting osteoblasts makes HDAC9 an interesting therapeutic target to support fracture healing and bone metabolisms. Full article
(This article belongs to the Special Issue Selected Papers from TERMIS European Chapter Meeting 2017 on “Biomechanics, Morphology and Imaging”)
►▼ Show Figures

Graphical abstract

Review

Jump to: Research

448 KiB  
Review
Shaping the Cell and the Future: Recent Advancements in Biophysical Aspects Relevant to Regenerative Medicine
by Melanie L. Hart, Jasmin C. Lauer, Mischa Selig, Martha Hanak, Brandan Walters and Bernd Rolauffs
J. Funct. Morphol. Kinesiol. 2018, 3(1), 2; https://doi.org/10.3390/jfmk3010002 - 22 Dec 2017
Cited by 33 | Viewed by 5876
Abstract
In a worldwide effort to generate clinically useful therapeutic or preventive interventions, harnessing biophysical stimuli for directing cell fate is a powerful strategy. With the vision to control cell function through engineering cell shape, better understanding, measuring, and controlling cell shape for ultimately [...] Read more.
In a worldwide effort to generate clinically useful therapeutic or preventive interventions, harnessing biophysical stimuli for directing cell fate is a powerful strategy. With the vision to control cell function through engineering cell shape, better understanding, measuring, and controlling cell shape for ultimately utilizing cell shape-instructive materials is an emerging “hot” topic in regenerative medicine. This review highlights how quantitation of cellular morphology is useful not only for understanding the effects of different microenvironmental or biophysical stimuli on cells, but also how it could be used as a predictive marker of biological responses, e.g., by predicting future mesenchymal stromal cell differentiation. We introduce how high throughput image analysis, combined with computational tools, are increasingly being used to efficiently and accurately recognize cells. Moreover, we discuss how a panel of quantitative shape descriptors may be useful for measuring specific aspects of cellular and nuclear morphology in cell culture and tissues. This review focuses on the mechano-biological principle(s) through which biophysical cues can affect cellular shape, and recent insights on how specific cellular “baseline shapes” can intentionally be engineered, using biophysical cues. Hence, this review hopes to reveal how measuring and controlling cellular shape may aid in future regenerative medicine applications. Full article
(This article belongs to the Special Issue Selected Papers from TERMIS European Chapter Meeting 2017 on “Biomechanics, Morphology and Imaging”)
►▼ Show Figures

Graphical abstract

Show export options expand_more Show export options expand_less
Select all
Export citation of selected articles as:
 
Displaying articles 1-5
Back to TopTop