Stem Cells Based Modeling with the Application in Tissue Engineering and Biomaterial Evaluation

A special issue of Pharmaceuticals (ISSN 1424-8247). This special issue belongs to the section "Biopharmaceuticals".

Deadline for manuscript submissions: closed (15 March 2023) | Viewed by 1945

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Department of Cardiac Thoracic and Vascular Sciences and Public Health, Italy LifeLab Torre della Ricerca, 5 piano sud , Corso Stati Uniti 4, 35127 Padua, Italy
Interests: Human induced pluripotent stem cells; disease modeling; organ regeneration; drug discovery; toxicity screening
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Special Issue Information

Dear Colleagues,

Stem cells have gained great attention in the field of drug discovery and regenerative medicine in recent years. The main advantage of technology, the ability to produce an identical copy of itself, and multipotency, i.e., the ability to generate cells different from itself, are fundamental characteristics of a stem cell. These are unique qualities that have allowed application in various diseases/disorders and medical challenges in both academia and industry—for instance, Parkinson’s disease, Alzheimer’s disease, diabetes, multiple sclerosis, heart disease, cancer, spinal cord injury, wound healing, and organ transplantation.

The prospect of performing high-throughput drug screening is aimed at the proliferation, directed differentiation, and toxicity and efficacy studies using stem cells. This seems to be a reliable platform for the drug discovery process. The discovery of induced pluripotent stem cells (hiPSCs) derived from normal or diseased tissue (human and animal) serves as a platform to perform drug screening aimed at developing cell-based therapies against conditions such as Parkinson’s disease and diabetes.

There are various research areas in which stem cell technology could make substantial contributions to the development and implementation of stem-cell-based models for toxicity testing. Increased use of human in vitro models of toxicity could reduce the use of animals in safety and risk assessment studies and offers the potential to dramatically enhance our understanding of the molecular basis of toxicity, leading to improved human models and assays for predicting biological response to drugs and environmental hazards.

Biomaterials are the substances, applied in various fields of medicines which are used to stay in constant contact with body tissues. The most frequently practiced example is tooth filling where most people first encounter biomaterials. The other most delicate examples like cardiac repair with heart valves, and joint replacements. Various categories of biomaterials have now been successfully developed and used for more than a generation. First-generation biomaterials largely depended on being inert, or relatively inert, with minimal tissue response. Despite the wide application and its usefulness in human health, nonspecific host immune response is always a challenge to encounter which are prone to infections. Modern biomaterials science provides a large array of biomaterial designs and surface modifications that modulate the host–material interactions to prevent an aggressive foreign-body response and at the same time avoid bacterial colonization. Furthermore, the use of biological motives in the new generations of biomaterials may elicit a specific immune response. Our special issue will cover following main aspects of the biomaterial application and characterization and proposition of new biomaterial, which could be animal and synthetic origin with less host-tissue immune responses.

  • New methods and protocol to develop to characterize the animal, human and synthetic origin tissues
  • Interaction of cells / stem cells and materials at the microenvironment
  • Materials as model systems for stem cell growth and modulation into tissue specific cells
  • (Nano)materials and (nano)systems for therapeutic delivery
  • biomimetic materials, including biologically inspired cell-inspired synthetic tools

Dr. Saima Imran
Guest Editor

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Keywords

  • stem cells
  • biomaterial
  • biocompatibility
  • regenerative medicine
  • tissue engineering
  • acellular matrix
  • decellularization
  • disease modeling

Published Papers (1 paper)

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Research

22 pages, 12022 KiB  
Article
Combinatorial Therapeutic Potential of Stem Cells and Benzimidazol Derivatives for the Reduction of Liver Fibrosis
by Maryam Iqbal, Sulaiman Shams, Huma Rafiq, Momin Khan, Shahid Khan, Umer Sadique Khattak, Sahib Gul Afridi, Fehmida Bibi, Angham Abdulrhman Abdulkareem and Muhammad Imran Naseer
Pharmaceuticals 2023, 16(2), 306; https://doi.org/10.3390/ph16020306 - 15 Feb 2023
Cited by 1 | Viewed by 1571
Abstract
(1) Background: Liver fibrosis is currently one of the top ten causes of death worldwide. Stem cells transplantation using mesenchymal stem cells (MSCs) is an alternative therapy which is used in the place of organ transplant, due to the incapacity of stem cells [...] Read more.
(1) Background: Liver fibrosis is currently one of the top ten causes of death worldwide. Stem cells transplantation using mesenchymal stem cells (MSCs) is an alternative therapy which is used in the place of organ transplant, due to the incapacity of stem cells to endure oxidative stress in the damage site, thus affecting the healing process. The present study aimed to enhance the therapeutic potential of MSCs using combined therapy, along with the novel synthetic compounds of benzimidazol derivatives. (2) Methods: Eighteen compound series (benzimidazol derivatives) were screened against liver fibrosis using an in vitro CCl4-induced injury model on cultured hepatocytes. IC50 values were calculated on the bases of LDH assay and cell viability assay. (3) Results: Among the eighteen compounds, compounds (10), (14) and (18) were selected on the basis of IC50 value, and compound (10) was the most potent and had the lowest IC50 value in the LDH assay (8.399 ± 0.23 uM) and cell viability assay (4.73 ± 0.37 uM). Next, these compounds were combined with MSCs using an in vitro hepatocytes injury culture and in vivo rat fibrotic model. The effect of the MSCs + compounds treatment on injured hepatocytes was evaluated using LDH assay, cell viability assay, GSH assay and real-time PCR analysis and immuno-staining for caspase-3. Significant reductions in LDH level, caspase-3 and apoptotic marker genes were noted in MSCs + compounds-treated injured hepatocytes. In vivo data also showed the increased homing of the MSCs, along with compounds after transplantation. Real-time PCR analysis and TUNEL assay results also support our study. (4) Conclusions: It was concluded that compounds (10), (14) and (18) can be used in combination with MSCs to reduce liver fibrosis. Full article
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