The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.
Restoration of senescent human diploid fibroblasts by modulation of the extracellular matrix
Abstract
Summary: Human diploid fibroblasts have the capacity to complete a finite number of cell divisions before entering a state of replicative senescence characterized by growth arrest, changes in morphology, and altered gene expression. Herein, we report that interaction with extracellular matrix (ECM) from young cells is sufficient to restore aged, senescent cells to an apparently youthful state. The identity of the restored cells as having been derived from senescent cells has been confirmed by a variety of methods, including time lapse live cell imaging and DNA finger print analysis. In addition to cell morphology, phenotypic restoration was assessed by resumption of proliferative potential, growth factor responsiveness, reduction of intracellular reactive oxygen species levels, recovery of mitochondrial membrane potential, and increased telomere length. Mechanistically, we find that both Ku and SIRT1 are induced during restoration and are required for senescent cells to return to a youthful phenotype. These observations demonstrate that human cellular senescence is profoundly influenced by cues from the ECM, and that senescent cell plasticity is much greater than that was previously believed to be the case.
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ECM prepared from young human fibroblasts induces a youthful state in aged senescent cells.
“Moreover, extracellular matrix prepared from young human fibroblasts induces a youthful state in aged senescent cells 252 .”
From Hallmarks of aging: An expanding universe (2023) · cites this paper as [252]
In human cells, extracellular matrix (ECM) from young fibroblasts rejuvenated aged senescent cells.
“| Altered intercellular communication | Human cells | ECM from young fibroblasts | Rejuvenation of aged senescent cells | 252”
From Hallmarks of aging: An expanding universe (2023) · cites this paper as [252]
Citations
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“This damage was undetectable in restored senescent cells or young cells (d’Adda di Fagagna et al., 2003).”
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Cited by
Sorted by citations
Hallmarks of aging: An expanding universe
López-Otín, C., Blasco, M. A., Partridge, L., Serrano, M., & Kroemer, G. (2023) · Cell · doi:10.1016/j.cell.2022.11.001 · Cited by 6,549
Physiological and pathological consequences of cellular senescence
Burton, D. G. A., & Krizhanovsky, V. (2014) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-014-1691-3 · Cited by 253
Connective tissue and fibroblast senescence in skin aging
Wlaschek, M., Maity, P., Makrantonaki, E., & Scharffetter-Kochanek, K. (2021) · Journal of Investigative Dermatology · doi:10.1016/j.jid.2020.11.010 · Cited by 245
Metadata
- Authors
- Choi, H. R., Cho, K. A., Kang, H. T., Lee, J. B., Kaeberlein, M., Suh, Y., Chung, I. K., & Park, S. C.
- Venue
- Aging Cell
- Publisher
- Wiley
- Published
- 2011-01-12
- Volume
- 10
- Issue
- 1
- Pages
- 148-157
- ISSN
- 1474-9718
- 1474-9726
- Cited by
- 84
- References
- 11
- Language
- en
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