Involvement of IGF binding protein 5 in prostaglandin E2-induced cellular senescence in human fibroblasts
Abstract
Inflammation is an underlying basis for the molecular alterations that link aging and age-related pathological processes. In a previous study, we found that secretory phospholipase A(2) (sPLA(2)) induced cellular senescence in human dermal fibroblasts (HDFs). To further investigate the association of inflammation with cellular senescence, the effects of PGE(2) on cellular senescence in HDFs were investigated, since PGE(2) is the most abundant prostanoid. PGE(2) treatment induces cellular senescence, as determined by a decrease in cell proliferation and an increase in senescence-associated β-galactosidase staining. Notably, PGE(2) treatment increased the IGFBP5 protein level. While treatment with PGE(2) antagonists repressed PGE(2)-induced cellular senescence, increasing intracellular cAMP accelerated cellular senescence. Down-regulation of IGFBP5 inhibited PGE(2)-induced cellular senescence. Taken together, these results suggest that PGE(2) may play an important role in controlling cellular senescence of HDFs through the regulation of IGFBP5 and therefore may contribute to inflammatory disorders associated with aging.
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These prostaglandins promote senescence and the SASP.
“These prostaglandins are known to promote senescence and the SASP135–137.”
From COVID-19 and cellular senescence (2023) · cites this paper as [135]
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- Authors
- Yang, H. H., Kim, C., Jung, B., Kim, K. S., & Kim, J.-R.
- Affiliations
- Yeungnam University College (KR)
- CHA University (KR)
- Korea Institute of Radiological and Medical Sciences (KR)
- Corresponding author
- Kim, Jae-Ryong
- ORCID
- Kim, Kwang Seok
- Venue
- Biogerontology
- Published
- 2010-12-30
- Volume
- 12
- Issue
- 3
- Pages
- 239-252
- ISSN
- 1389-5729 (ISSN-L)
- 1573-6768
- OpenAlex
- W2066115027
- Cited by
- 22
- References
- 53
- Citations by year
- 2026: 1 · 2024: 2 · 2023: 1 · 2022: 3 · 2021: 1 · 2020: 2 · 2019: 2 · 2017: 2 · 2016: 1 · 2015: 2 · 2014: 1 · 2013: 3 · 2012: 1
- FWCI
- 0.87
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Biogerontology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Physiology › Telomeres, Telomerase, and Senescence
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Aging › Genetics, Aging, and Longevity in Model Organisms
- Health Sciences › Medicine › Dermatology › Skin Protection and Aging
- Keywords
- IGF binding protein-5, prostaglandin E2, cellular senescence, human dermal fibroblasts, inflammation, aging, cAMP signaling, senescence-associated β-galactosidase, secretory phospholipase A2
- MeSH terms
- Base Sequence, Cells, Cultured, Fibroblasts, Humans, Promoter Regions, Genetic, Skin, Blotting, Western, Dinoprostone, Cellular Senescence, DNA Primers, Insulin-Like Growth Factor Binding Protein 5, Reverse Transcriptase Polymerase Chain Reaction
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