Literature DB >> 23745554

Adult stem cells and biocompatible scaffolds as smart drug delivery tools for cardiac tissue repair.

Stefania Pagliari1, Sara Romanazzo, Diogo Mosqueira, Perpetua Pinto-do-Ó, Takao Aoyagi, Giancarlo Forte.   

Abstract

The contribution of adult stem cells to cardiac repair is mostly ascribed to an indirect paracrine effect, rather than to their actual engraftment and differentiation into new contractile and vascular cells. This effect consists in a direct reduction of host cell death, promotion of neovascularization, and in a "bystander effect" on local inflammation. A number of cytokines secreted by adult stem/progenitor cells has been proposed to be responsible for the consistent beneficial effect reported in the early attempts to deliver different stem cell subsets to the injured myocardium. Aiming to maximize their beneficial activity on the diseased myocardium, the genetic modification of adult stem cells to enhance and/or control the secretion of specific cytokines would turn them into active drug delivery vectors. On the other hand, engineering biocompatible scaffolds as to release paracrine factors could result in multiple advantages: (1) achieve a local controlled release of the drug of interest, thus minimizing off-target effects, (2) enhance stem cell retention in the injured area and (3) boost the beneficial paracrine effects exerted by adult stem cells on the host tissue. In the present review, a critical overview of the state-of-the-art in the modification of stem cells and the functionalization of biocompatible scaffolds to deliver beneficial soluble factors to the injured myocardium is offered. Besides the number of concerns to be addressed before a clinical application can be foreseen for such concepts, this path could translate into the generation of active scaffolds as smart cell and drug delivery systems for cardiac repair.

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Year:  2013        PMID: 23745554     DOI: 10.2174/09298673113209990032

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  6 in total

1.  Human umbilical cord tissue-derived mesenchymal stromal cells attenuate remodeling after myocardial infarction by proangiogenic, antiapoptotic, and endogenous cell-activation mechanisms.

Authors:  Diana Santos Nascimento; Diogo Mosqueira; Luís Moura Sousa; Mariana Teixeira; Mariana Filipe; Tatiana Pinho Resende; Ana Francisca Araújo; Mariana Valente; Joana Almeida; José Paulo Martins; Jorge Miguel Santos; Rita Nogueira Bárcia; Pedro Cruz; Helder Cruz; Perpétua Pinto-do-Ó
Journal:  Stem Cell Res Ther       Date:  2014-01-10       Impact factor: 6.832

2.  High-Throughput Phenotyping Toolkit for Characterizing Cellular Models of Hypertrophic Cardiomyopathy In Vitro.

Authors:  Diogo Mosqueira; Katarzyna Lis-Slimak; Chris Denning
Journal:  Methods Protoc       Date:  2019-10-26

3.  A multistep procedure to prepare pre-vascularized cardiac tissue constructs using adult stem sells, dynamic cell cultures, and porous scaffolds.

Authors:  Stefania Pagliari; Annalisa Tirella; Arti Ahluwalia; Sjoerd Duim; Marie-Josè Goumans; Takao Aoyagi; Giancarlo Forte
Journal:  Front Physiol       Date:  2014-06-03       Impact factor: 4.566

4.  Transfection of hPSC-Cardiomyocytes Using Viafect™ Transfection Reagent.

Authors:  Sara E Bodbin; Chris Denning; Diogo Mosqueira
Journal:  Methods Protoc       Date:  2020-08-09

5.  Mitochondrial DNA: Hotspot for Potential Gene Modifiers Regulating Hypertrophic Cardiomyopathy.

Authors:  Parisa K Kargaran; Jared M Evans; Sara E Bodbin; James G W Smith; Timothy J Nelson; Chris Denning; Diogo Mosqueira
Journal:  J Clin Med       Date:  2020-07-23       Impact factor: 4.964

6.  Isogenic models of hypertrophic cardiomyopathy unveil differential phenotypes and mechanism-driven therapeutics.

Authors:  Jamie R Bhagwan; Diogo Mosqueira; Karolina Chairez-Cantu; Ingra Mannhardt; Sara E Bodbin; Mine Bakar; James G W Smith; Chris Denning
Journal:  J Mol Cell Cardiol       Date:  2020-06-10       Impact factor: 5.000

  6 in total

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