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Knockdown of moesin expression accelerates cellular senescence of human dermal microvascular endothelial cells

Authors
 Ju Hee Lee  ;  Jung Hoan Yoo  ;  Sang Ho Oh  ;  Kyu-Yeop Lee  ;  Kwang Hoon Lee 
Citation
 YONSEI MEDICAL JOURNAL, Vol.51(3) : 438-447, 2010 
Journal Title
 YONSEI MEDICAL JOURNAL 
ISSN
 0513-5796 
Issue Date
2010
MeSH
Aged, 80 and over ; Blotting, Western ; Cell Line ; Cellular Senescence/genetics ; Cellular Senescence/physiology* ; Child ; Endothelial Cells/cytology* ; Endothelial Cells/metabolism* ; Humans ; Immunohistochemistry ; In Vitro Techniques ; Microfilament Proteins/genetics ; Microfilament Proteins/physiology* ; Microscopy, Phase-Contrast ; Microvessels/cytology* ; Platelet Endothelial Cell Adhesion Molecule-1/metabolism ; RNA, Small Interfering/genetics ; RNA, Small Interfering/physiology ; Reverse Transcriptase Polymerase Chain Reaction ; Skin/blood supply*
Keywords
Aging ; endothelial cell ; shRNA lentivirus ; moesin ; p16
Abstract
PURPOSE: Endothelial cells maintain the homeostasis of blood, which consists of plasma and cellular components, and regulate the interaction between blood and the surrounding tissues. They also have essential roles in vascular permeability, the circulation, coagulation, inflammation, wound healing, and tissue growth. The senescence of endothelial cells is closely related to the aging of the adjacent tissues and to age-related vascular disease. Recently, the expression of moesin was found to be decreased in elderly human dermal microvascular endothelial cells (HDMECs), and an association between moesin and senescence has been suggested. This study examined the functional role of moesin in cellular senescence. MATERIALS AND METHODS: To study the effects of decreased moesin expression on cellular senescence and metabolism, HDMECs were transfected with short hairpin-RNA (shRNA) lentivirus to silence moesin gene expression. In addition, specimens from young and old human skin were stained with antimoesin and anti-p16 antibodies as an in vivo study. RESULTS: Using shRNAlentivirus, moesin knock-down HDMECs developed characteristics associated with aging and expressed senescence associated-beta-galactosidase during early passages. They also showed increased p16 expression, decreased metabolic activity, and cell growth retardation. Human skin tissue from elderly persons showed decreased moesin expression and increased p16 expression. CONCLUSION: These findings suggest that there is a functional association between moesin expression and cellular senescence. Further study of the functional mechanism of moesin in the cytoskeleton and cellular senescence is needed. In addition, this study provides a useful model for developing anti-aging treatments.
Files in This Item:
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DOI
10.3349/ymj.2010.51.3.438
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Dermatology (피부과학교실) > 1. Journal Papers
Yonsei Authors
Oh, Sang Ho(오상호) ORCID logo https://orcid.org/0000-0002-4477-1400
Lee, Kwang Hoon(이광훈)
Lee, Ju Hee(이주희) ORCID logo https://orcid.org/0000-0002-1739-5956
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/100877
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