Literature DB >> 33585579

Mitochondrial Medicine: Genetic Underpinnings and Disease Modeling Using Induced Pluripotent Stem Cell Technology.

Parisa K Kargaran1, Diogo Mosqueira2, Tamas Kozicz3.   

Abstract

Mitochondrial medicine is an exciting and rapidly evolving field. While the mitochondrial genome is small and differs from the nuclear genome in that it is circular and free of histones, it has been implicated in neurodegenerative diseases, type 2 diabetes, aging and cardiovascular disorders. Currently, there is a lack of efficient treatments for mitochondrial diseases. This has promoted the need for developing an appropriate platform to investigate and target the mitochondrial genome. However, developing these therapeutics requires a model system that enables rapid and effective studying of potential candidate therapeutics. In the past decade, induced pluripotent stem cells (iPSCs) have become a promising technology for applications in basic science and clinical trials, and have the potential to be transformative for mitochondrial drug development. Engineered iPSC-derived cardiomyocytes (iPSC-CM) offer a unique tool to model mitochondrial disorders. Additionally, these cellular models enable the discovery and testing of novel therapeutics and their impact on pathogenic mtDNA variants and dysfunctional mitochondria. Herein, we review recent advances in iPSC-CM models focused on mitochondrial dysfunction often causing cardiovascular diseases. The importance of mitochondrial disease systems biology coupled with genetically encoded NAD+/NADH sensors is addressed toward developing an in vitro translational approach to establish effective therapies.
Copyright © 2021 Kargaran, Mosqueira and Kozicz.

Entities:  

Keywords:  cardiomyocytes; drug discovery; human induced pluripotent stem cells; mitochondrial disease; regenerative medicine; sonar sensor

Year:  2021        PMID: 33585579      PMCID: PMC7874022          DOI: 10.3389/fcvm.2020.604581

Source DB:  PubMed          Journal:  Front Cardiovasc Med        ISSN: 2297-055X


  136 in total

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Review 3.  Sarcoplasmic reticulum-mitochondria communication in cardiovascular pathophysiology.

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Journal:  Nature       Date:  1981-04-09       Impact factor: 49.962

5.  Rational design of a high-affinity, fast, red calcium indicator R-CaMP2.

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Authors:  Matthew S Elitt; Lilianne Barbar; Paul J Tesar
Journal:  Hum Mol Genet       Date:  2018-08-01       Impact factor: 6.150

7.  A bacterial cytidine deaminase toxin enables CRISPR-free mitochondrial base editing.

Authors:  Beverly Y Mok; Marcos H de Moraes; Jun Zeng; Dustin E Bosch; Anna V Kotrys; Aditya Raguram; FoSheng Hsu; Matthew C Radey; S Brook Peterson; Vamsi K Mootha; Joseph D Mougous; David R Liu
Journal:  Nature       Date:  2020-07-08       Impact factor: 49.962

8.  Fatty Acids Enhance the Maturation of Cardiomyocytes Derived from Human Pluripotent Stem Cells.

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Journal:  Stem Cell Reports       Date:  2019-09-26       Impact factor: 7.765

Review 9.  Maturation of Cardiac Energy Metabolism During Perinatal Development.

Authors:  Jérôme Piquereau; Renée Ventura-Clapier
Journal:  Front Physiol       Date:  2018-07-19       Impact factor: 4.566

10.  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

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  1 in total

Review 1.  Regulation of energy metabolism in human pluripotent stem cells.

Authors:  Weiwei Liu; Guokai Chen
Journal:  Cell Mol Life Sci       Date:  2021-11-13       Impact factor: 9.261

  1 in total

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