Study highlights the robustness of miRNA modulation during aging process

Learn anything. Thousands of top courses to choose from.
Clinical Trials & Research

Aging-US published “miRNAs generated from Meg3-Mirg locus are downregulated during aging” which reported that Aging determines a multilevel functional decline and increases the risk for cardiovascular pathologies.

The heart is one of the most affected organs in aged individuals, however little is known about the extent and robustness to which miRNA profiles are modulated in cardiac cells during aging. This paper provides a comprehensive characterization of the aging-associated miRNA profile in the murine cardiac fibroblasts, which are increasingly recognized for their active involvement in cardiac physiology and pathology.

Next-generation sequencing of cardiac fibroblasts isolated from young and old mice revealed that an important fraction of the miRNAs generated by the Meg3-Mirg locus was downregulated during aging. To address the specificity of this repression, four miRNAs selected as representative for this locus were further assessed in other cells and organs isolated from aged mice.

The results suggested that the repression of miRNAs generated by the Meg3-Mirg locus was a general feature of aging in multiple organs.

In conclusion, this study published in Aging-US, provides new data concerning the mechanisms of natural aging and highlights the robustness of the miRNA modulation during this process.

Aging is a universal, multifactorial and progressive process determined by an intrinsic decreased ability of the organism to counterbalance the adverse effects of accumulating extrinsic risk factors.”

Dr Alexandrina Burlacu, The Institute of Cellular Biology and Pathology, “Nicolae Simionescu”

Non-myocytes include multiple cell types, among which the cardiac fibroblasts, which are a heterogeneous and dynamic group of cells with important contributions to cardiac function, in healthy and diseased states.

These findings demonstrate that the cardiac fibroblast is a unique cell type that retains its embryological cardiac identity and has a critical role in the maintenance of the cardiac tissue.

Aging-related changes in gene expression are more pronounced in cardiac fibroblasts than in other cardiac cells and they mostly affect the inflammation, extracellular matrix organization and angiogenesis.

While miRNAs regulate different aspects of cardiovascular biology, little is known about the extent to which miRNA profile is modulated during aging in cardiac fibroblasts and whether the aging-associated dysregulation of miRNA profile is cell-specific or widespread.

The aims of this study were:

  1. To identify relevant features of the aging-associated miRNA profile in murine cardiac fibroblasts and;
  2. To determine the cell and organ specificity of the aging-associated miRNA changes found in cardiac fibroblasts.

The Burlacu Research Team concluded in their Aging-US Research Output, “this study provides evidence that aging is associated to the downregulation of miRNAs generated by the Meg3-Mirg locus in several cell types and organs. This is likely to be a common and biologically meaningful response in aging, however additional studies are required to determine whether it is universally associated with this process. Such insights may advance the understanding of the mechanisms of aging, being of general interest in the field of geroscience.”

Journal reference:

Lupan, A-M., et al. (2021) miRNAs generated from Meg3-Mirg locus are downregulated during aging. Aging. doi.org/10.18632/aging.203208.

Articles You May Like

FDA OKs Pfizer COVID Booster for 65 and Over, Those at High Risk
Examining the Underpinnings of COVID Anti-Vaccine Sentiment
Firefighter Advocates For Men’s Health While He Battles Breast Cancer In ICU
Scientists characterize new genetic variants that cause nonsyndromic neurodevelopmental disorder
Making the most of your ‘eureka’ moment: getting from the science to the clinic

Leave a Reply

Your email address will not be published. Required fields are marked *