Abstract

Simple SummaryDistinct tissue engineering strategies are currently being developed. Cell-based therapies, implantation of synthetic scaffolds or combination of a scaffold with seeded cells are being used according to the biologic premises. Mitochondria play a central role in cell life cycle due to their preponderant role in energy production. Recent data suggest that small non-coding RNAs encoded by mitochondria DNA such as microRNAs regulate a plethora of factors and consequently signaling pathways, crucial in disease pathogenesis and also putatively in regenerative processes. Unveiling mitochondrial microRNAs biological function and their targets will propel the development of innovative therapeutic and diagnostic tools.The most famous role of mitochondria is to generate ATP through oxidative phosphorylation, a metabolic pathway that involves a chain of four protein complexes (the electron transport chain, ETC) that generates a proton-motive force that in turn drives the ATP synthesis by the Complex V (ATP synthase). An impressive number of more than 1000 mitochondrial proteins have been discovered. Since mitochondrial proteins have a dual genetic origin, it is predicted that ~99% of these proteins are nuclear-encoded and are synthesized in the cytoplasmatic compartment, being further imported through mitochondrial membrane transporters. The lasting 1% of mitochondrial proteins are encoded by the mitochondrial genome and synthesized by the mitochondrial ribosome (mitoribosome). As a result, an appropriate regulation of mitochondrial protein synthesis is absolutely required to achieve and maintain normal mitochondrial function. Regarding miRNAs in mitochondria, it is well-recognized nowadays that several cellular mechanisms involving mitochondria are regulated by many genetic players that originate from either nuclear- or mitochondrial-encoded small noncoding RNAs (sncRNAs). Growing evidence collected from whole genome and transcriptome sequencing highlight the role of distinct members of this class, from short interfering RNAs (siRNAs) to miRNAs and long noncoding RNAs (lncRNAs). Some of the mechanisms that have been shown to be modulated are the expression of mitochondrial proteins itself, as well as the more complex coordination of mitochondrial structure and dynamics with its function. We devote particular attention to the role of mitochondrial miRNAs and to their role in the modulation of several molecular processes that could ultimately contribute to tissue regeneration accomplishment.

Highlights

  • Simple Summary: Distinct tissue engineering strategies are currently being developed

  • Growing evidence collected from whole genome and transcriptome sequencing highlight the role of distinct members of this class, from short interfering RNAs to miRNAs and long noncoding RNAs

  • (19–23 nucleotides) that represent a new level of control of gene expression. miRNAs act at the post-transcriptional level to modulate protein-coding genes, either by blocking the translation of messenger RNA or by actively encouraging its degradation, and it is well reported that each miRNA can target multiple genes [47]

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Summary

Regenerative Biology

Regeneration is the ability of animals to restore, either partially or entirely, tissues or organs that were damaged due to trauma [1]. Human stem cells can be classified into tissue-specific progenitor stem cells (TSPSCs), embryonic stem cells (ESCs), umbilical cord stem cells (UCSCs), mesenchymal stem cells (MSCs) and induced pluripotent stem cells (iPSCs) [12]. 963 studies, either completed or in phases 3/4, use stem cells and address a wide array of diseases and pathological conditions (wound healing, infertility, bone regeneration, etc.). From those studies, only 9 involve the use of a scaffold or a matrix to support and deliver the cells, suggesting that the field of biomaterials still has a path to travel before its clinical reality (www.clinicaltrial.gov)

Mitochondria miRNA Biology
Modulation
Mitochondrial miRNAs—Potential Contribution for Regeneration
Mitochondrial
Emerging Therapies in Regenerative Medicine
Findings
Conclusions
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