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Monnuclear sequencing revealed 7 unique cell types and differences in gene expression with age
.
"Our study provides some insights
into human skeletal muscle aging.
"
A new research paper is published on the cover of Aging (listed as "Aging (Albany NY)" by Medline/PubMed and "Aging-US" by Web of Science), Volume 14, Issue 23
.
Aging is accompanied by a loss of muscle mass and function, called sarcopenia, which causes a variety of diseases and economic burdens
in the human population.
Mechanisms associated with age-related sarcopenia or weakness include inflammation, loss of muscle stem cells, mitochondrial dysfunction, and loss of motor neurons, but whether there are key drivers of sarcopenia is unknown
.
In the new study, researchers performed lower extremity muscle biopsies on 72 young, elderly, and frail human subjects, transcriptome analysis using bulk RNA-seq (N = 72) and mononuclear RNA-seq (N = 17) to gain a deeper understanding of age-related muscle loss
.
"This combined approach reveals changes in gene expression with age and weakness in multiple cell types, including mature skeletal muscle
.
"
Notably, the researchers found that in aging muscle, expression of the MYH8 and PDK4 genes increased, and expression of the IGFN1 gene decreased
.
They used digital spatial analysis to validate changes
in several key genes in fixed human muscle tissue.
The researchers also found a small subset of cells expressing CDKN1A, present only in older samples, consistent with
p21cip1-driven aging in this subpopulation.
"Overall, our findings identify unique cell subsets in senile and oligoskeletal muscle, which will facilitate the development of new therapeutic strategies to combat age-related weakness
.
"