Calcification in Werner syndrome associated with lymphatic vessels aging.


Journal

Aging
ISSN: 1945-4589
Titre abrégé: Aging (Albany NY)
Pays: United States
ID NLM: 101508617

Informations de publication

Date de publication:
27 12 2021
Historique:
received: 07 06 2021
accepted: 10 12 2021
pubmed: 28 12 2021
medline: 1 2 2022
entrez: 27 12 2021
Statut: ppublish

Résumé

In addition to the symptoms of aging, the main symptoms in Werner syndrome (WS), a hereditary premature aging disease, include calcification of subcutaneous tissue with solid pain and refractory skin ulcers. However, the mechanism of calcification in WS remains unclear. In this study, the histological analysis of the skin around the ulcer with calcification revealed an accumulation of calcium phosphate in the lymphatic vessels. Moreover, the morphological comparison with the lymphatic vessels in PAD patients with chronic skin ulcers demonstrated the ongoing lymphatic remodeling in WS patients because of the narrow luminal cross-sectional area (LA) of the lymphatic vessels but the increment of lymphatic microvessels density (MLVD). Additionally, fluorescence immunohistochemical analysis presented the cytoplasmic distribution and the accumulation of WRN proteins in endothelial cells on remodeling lymphatic vessels. In summary, these results point out a relationship between calcification in lymphatic vessels and the remodeling of lymphatic vessels and suggest the significance of the accumulation of WRN mutant proteins as an age-related change in WS patients. Thus, cytoplasmic accumulation of WRN protein can be an indicator of the decreasing drainage function of the lymphatic vessels and the increased risk of skin ulcers and calcification in the lymphatic vessels.

Identifiants

pubmed: 34958633
pii: 203789
doi: 10.18632/aging.203789
pmc: PMC8751599
doi:

Substances chimiques

WRN protein, human EC 3.6.4.12
Werner Syndrome Helicase EC 3.6.4.12

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

25717-25728

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Auteurs

Hideyuki Ogata (H)

Department of Plastic, Reconstructive, and Aesthetic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.

Shinsuke Akita (S)

Department of Plastic, Reconstructive, and Aesthetic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.

Sanae Ikehara (S)

Department of Pathology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Cellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan.

Kazuhiko Azuma (K)

Cellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan.

Takashi Yamaguchi (T)

Cellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan.

Maihulan Maimaiti (M)

Department of Pathology, Graduate School of Medicine, Chiba University, Chiba, Japan.

Yoshiro Maezawa (Y)

Department of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Division of Diabetes, Metabolism and Endocrinology, Chiba University Hospital, Chiba, Japan.

Yoshitaka Kubota (Y)

Department of Plastic, Reconstructive, and Aesthetic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.

Koutaro Yokote (K)

Department of Endocrinology, Hematology and Gerontology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Division of Diabetes, Metabolism and Endocrinology, Chiba University Hospital, Chiba, Japan.

Nobuyuki Mitsukawa (N)

Department of Plastic, Reconstructive, and Aesthetic Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.

Yuzuru Ikehara (Y)

Department of Pathology, Graduate School of Medicine, Chiba University, Chiba, Japan.
Cellular and Molecular Biotechnology Research Institute, National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan.

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