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. 2024 May 7;14(5):593.
doi: 10.3390/life14050593.

Matrisome Transcriptome Dynamics during Tissue Aging

Affiliations

Matrisome Transcriptome Dynamics during Tissue Aging

Zulfiya G Guvatova et al. Life (Basel). .

Abstract

The extracellular matrix (ECM) is a complex three-dimensional network of macromolecules that provides structural support for the cells and plays a significant role in tissue homeostasis and repair. Growing evidence indicates that dysregulation of ECM remodeling contributes to various pathological conditions in the body, including age-associated diseases. In this work, gene expression data of normal human tissues obtained from the Genotype-Tissue Expression project, as well as data from MatrisomeDB 2.0, the ECM-protein knowledge database, are used to estimate the age-dependent matrisome transcriptome dynamics in the blood, heart, brain, liver, kidneys, lungs, and muscle. Differential gene expression (DE) analysis revealed dozens of matrisome genes encoding both structural elements of the ECM and ECM-associated proteins, which had a tissue-specific expression profile with age. Among common DE genes that changed expression with age in at least three tissues, COL18A1, MFAP1, IGFBP7, AEBP1, LTBP2, LTBP4, LG14, EFEMP1, PRELP, BGN, FAM20B, CTSC, CTSS, and CLEC2B were observed. The findings of the study also reveal that there are sex-specific alterations during aging in the matrisome gene expression. Taken together, the results obtained in this work may help in understanding the role of the ECM in tissue aging and might prove valuable for the future development of the field of ECM research in general.

Keywords: RNA-Seq; aging; extracellular matrix; gene expression; matrisome; tissue aging; transcriptome.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Commonly upregulated and downregulated matrisome genes with age in at least three tissues (LogCPM > 2, p < 0.05) in (a) female and (b) male groups. Common genes that changed expression with age in both sexes are circled in red.
Figure 2
Figure 2
STRING networks (including physical interactions, co-expression, co-occurrence in databases, etc.) for genes whose expression was significantly associated with age in (a) female and (b) male groups. Every color corresponds to a cluster.

References

    1. Bonnans C., Chou J., Werb Z. Remodelling the Extracellular Matrix in Development and Disease. Nat. Rev. Mol. Cell. Biol. 2014;15:786–801. doi: 10.1038/nrm3904. - DOI - PMC - PubMed
    1. Fedintsev A., Moskalev A. Stochastic Non-Enzymatic Modification of Long-Lived Macromolecules—A Missing Hallmark of Aging. Ageing Res. Rev. 2020;62:101097. doi: 10.1016/j.arr.2020.101097. - DOI - PubMed
    1. Chen C., Zhang J.-Q., Li L., Guo M., He Y., Dong Y., Meng H., Yi F. Advanced Glycation End Products in the Skin: Molecular Mechanisms, Methods of Measurement, and Inhibitory Pathways. Front. Med. 2022;9:837222. doi: 10.3389/fmed.2022.837222. - DOI - PMC - PubMed
    1. Mallipattu S.K., Uribarri J. Advanced Glycation End Product Accumulation. Curr. Opin. Nephrol. Hypertens. 2014;23:547–554. doi: 10.1097/MNH.0000000000000062. - DOI - PMC - PubMed
    1. Li Z., Wang X., Hong T., Wang H., Gao Z., Wan M. Advanced Glycosylation End Products Inhibit the Proliferation of Bone-Marrow Stromal Cells through Activating MAPK Pathway. Eur. J. Med. Res. 2021;26:94. doi: 10.1186/s40001-021-00559-x. - DOI - PMC - PubMed

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