Advances in Regenerative Medicine and Tissue Engineering

A special issue of Processes (ISSN 2227-9717). This special issue belongs to the section "Pharmaceutical Processes".

Deadline for manuscript submissions: closed (30 June 2021) | Viewed by 8473

Special Issue Editors


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Guest Editor
Department of Life Sciences and Systems Biology, University of Torino, 10123 Turin, Italy
Interests: biomaterials; bone regeneration and differentiation; MSCs differentiation; bone prosthesis materials; bioreactor; organ-on-chip; TRP channels

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Guest Editor
CIR Dental School, Department of Surgical Sciences, University of Turin, Turin, Italy
Interests: bone regeneration; biomaterials; dental implants; MSCs differentiation; bone substitute materials; biological interfaces
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Special Issue Information

Dear Colleagues,

Tissues and organs of the body have both structure and function, therefore in tissue engineering any proposed approach must be able to mimic the morphology and characteristics of the original tissue or be able to stimulate the regeneration of the original tissue. In regenerative medicine, it is important to consider many aspects such as the material used, the structure of the scaffold, the growth factors, and the cell populations, in particular stem cells.

For example, with more than 2 million bone grafts performed annually worldwide, bone reconstruction is a primary task of regenerative medicine, which may rely on a growing variety of sources of stem cells suitable for autologous transplants. Notwithstanding the remarkable advancements in bone regeneration techniques and the great potential of mesenchymal stem cells (MSCs), the treatment of critical-sized defects with tissue engineering has yet to be achieved. Human mesenchymal stem cells have been shown to be particularly suitable for auto-transplant procedures. Apart from bone marrow, MSCs can be obtained from the umbilical cord, adipose tissue, the placenta, the human synovial membrane, and the dental pulp of deciduous teeth. Independently of the type of grafting, the challenge in bone tissue engineering is represented by critical-sized bone defect, i.e., larger bone defects, and osseous injuries unable to heal spontaneously.

Only through an integrated approach will multidisciplinary teams succeed in fabricating complex scaffolds, including live cell populations endowed with the most sophisticated features of biomimicry. Indeed, tissue formation requires different cell populations to cooperate to set up a complex 3D tissue under the guidance of bio-mechanical cues.

This Special Issue on bone and tissue regeneration aims to highlight the new approach of treatment based on the comprehension of the physiology and the interplay between different cell types. Topics include but are not limited to the following:

  • Use of MSCs in regenerative medicine;
  • Control of angiogenesis in tissue regeneration;
  • New approaches of MSC isolation from different sources;
  • Bioactive bone substitution.

Dr. Tullio Genova
Prof. Federico Mussano
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. Processes is an international peer-reviewed open access monthly 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 2400 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

  • tissue regenerations
  • mesenchymal stem cells
  • adipose-derived stem cells
  • bone differentiation
  • angiogenesis
  • tissue vascularization
  • bioreactor
  • 3D culture
  • bone scaffold
  • bone graft

Published Papers (2 papers)

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Research

13 pages, 7884 KiB  
Article
Electrophysiological Effects of Extracellular Vesicles Secreted by Cardiosphere-Derived Cells: Unraveling the Antiarrhythmic Properties of Cell Therapies
by Lidia Gómez-Cid, Marina Moro-López, Ana S. de la Nava, Ismael Hernández-Romero, Ana I. Fernández, Susana Suárez-Sancho, Felipe Atienza, Lilian Grigorian-Shamagian and Francisco Fernández-Avilés
Processes 2020, 8(8), 924; https://0-doi-org.brum.beds.ac.uk/10.3390/pr8080924 - 02 Aug 2020
Cited by 5 | Viewed by 3802
Abstract
Although cell-based therapies show potential antiarrhythmic effects that could be mediated by their paracrine action, the mechanisms and the extent of these effects were not deeply explored. We investigated the antiarrhythmic mechanisms of extracellular vesicles secreted by cardiosphere-derived cell extracellular vesicles (CDC-EVs) on [...] Read more.
Although cell-based therapies show potential antiarrhythmic effects that could be mediated by their paracrine action, the mechanisms and the extent of these effects were not deeply explored. We investigated the antiarrhythmic mechanisms of extracellular vesicles secreted by cardiosphere-derived cell extracellular vesicles (CDC-EVs) on the electrophysiological properties and gene expression profile of HL1 cardiomyocytes. HL-1 cultures were primed with CDC-EVs or serum-free medium alone for 48 h, followed by optical mapping and gene expression analysis. In optical mapping recordings, CDC-EVs reduced the activation complexity of the cardiomyocytes by 40%, increased rotor meandering, and reduced rotor curvature, as well as induced an 80% increase in conduction velocity. HL-1 cells primed with CDC-EVs presented higher expression of SCN5A, CACNA1C, and GJA1, coding for proteins involved in INa, ICaL, and Cx43, respectively. Our results suggest that CDC-EVs reduce activation complexity by increasing conduction velocity and modifying rotor dynamics, which could be driven by an increase in expression of SCN5A and CACNA1C genes, respectively. Our results provide new insights into the antiarrhythmic mechanisms of cell therapies, which should be further validated using other models. Full article
(This article belongs to the Special Issue Advances in Regenerative Medicine and Tissue Engineering)
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9 pages, 1711 KiB  
Article
A Novel Method to Optimize Autologous Adipose Tissue Recovery with Extracellular Matrix Preservation
by Ilaria Roato, Federico Mussano, Simone Reano, Filippo Boriani, Andrea Margara, Riccardo Ferracini, Ezio Adriani, Omar Sabry, Mauro Fiorini and Paolo Fattori
Processes 2020, 8(1), 88; https://0-doi-org.brum.beds.ac.uk/10.3390/pr8010088 - 09 Jan 2020
Cited by 6 | Viewed by 3799 | Correction
Abstract
This work aims to characterize a new method to recover low-manipulated human adipose tissue, enriched with adipose tissue-derived mesenchymal stem cells (ATD-MSCs) for autologous use in regenerative medicine applications. Lipoaspirated fat collected from patients was processed through Lipocell, a Class II-a medical device [...] Read more.
This work aims to characterize a new method to recover low-manipulated human adipose tissue, enriched with adipose tissue-derived mesenchymal stem cells (ATD-MSCs) for autologous use in regenerative medicine applications. Lipoaspirated fat collected from patients was processed through Lipocell, a Class II-a medical device for dialysis of adipose tissue, by varying filter sizes and washing solutions. ATD-MSC yield was measured with flow cytometry after stromal vascular fraction (SVF) isolation in fresh and cultured samples. Purification from oil and blood was measured after centrifugation with spectrophotometer analysis. Extracellular matrix preservation was assessed through hematoxylin and eosin (H&E) staining and biochemical assay for total collagen, type-2 collagen, and glycosaminoglycans (GAGs) quantification. Flow cytometry showed a two-fold increase of ATD-MSC yield in treated samples in comparison with untreated lipoaspirate; no differences where reported when varying filter size. The association of dialysis and washing thoroughly removed blood and oil from samples. Tissue architecture and extracellular matrix integrity were unaltered after Lipocell processing. Dialysis procedure associated with Ringer’s lactate preserves the proliferation ability of ATD-MSCs in cell culture. The characterization of the product showed that Lipocell is an efficient method for purifying the tissue from undesired byproducts and preserving ATD-MSC vitality and extracellular matrix (ECM) integrity, resulting in a promising tool for regenerative medicine applications. Full article
(This article belongs to the Special Issue Advances in Regenerative Medicine and Tissue Engineering)
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