A novel peptide 'T14' reflects age and photo-aging in human skin.
acetylcholinesterase peptide
age
keratinocyte
photo-aging
skin
Journal
Aging
ISSN: 1945-4589
Titre abrégé: Aging (Albany NY)
Pays: United States
ID NLM: 101508617
Informations de publication
Date de publication:
28 06 2023
28 06 2023
Historique:
received:
23
01
2023
accepted:
09
06
2023
medline:
7
7
2023
pubmed:
29
6
2023
entrez:
29
6
2023
Statut:
ppublish
Résumé
T14 is a 14mer peptide derived from the C-terminus of acetylcholinesterase (AChE). Once cleaved, it is independently bioactive of the parent molecule and enhances calcium influx in different cell types, in a range of scenarios: it binds to an allosteric site selectively on the alpha-7 receptor, where it modulates calcium influx and is thus a potential trophic agent, as already reported in a range of normal developmental scenarios. However, if inappropriately activated, this erstwhile beneficial effect converts to a toxic one, resulting in pathologies as disparate as Alzheimer's and various metastatic cancers. Given that epidermal keratinocyte cells have the same ectodermal origin as brain cells, as well as expressing AChE and the alpha-7 receptor, we have explored whether T14 plays a comparable role. Here we report that the T14 immunoreactivity is detectable in human keratinocytes with levels inversely related to age: this decrease is even more apparent with chronic photo-exposure and thus accelerated skin aging. We conclude that T14, an agent promoting cell growth and renewal in other parts of the body, also operates in skin, Moreover, monitoring of keratinocyte T14 levels might offer further insights into the now well reported link between degenerative diseases and epidermal cell profile.
Identifiants
pubmed: 37382595
pii: 204844
doi: 10.18632/aging.204844
pmc: PMC10333063
doi:
Substances chimiques
Acetylcholinesterase
EC 3.1.1.7
Peptide Fragments
0
Calcium
SY7Q814VUP
Peptides
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
5279-5289Références
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