| Literature DB >> 29070775 |
Daiki Takahashi1,2, Hiroaki Suzuki2, Yasumasa Kakei2, Kimi Yamakoshi3, Yasuhiro Minami1, Takahide Komori2, Michiru Nishita1.
Abstract
The submandibular gland (SMG) is one of the major salivary glands that play important roles for variety of physiological functions, such as digestion of foods, prevention of infection, and lubrication of the mouth. Dysfunction of the SMG, often associated with a salivary inflammation, adversely influences a person's quality of life. However, the mechanism underlying inflammation-driven dysfunction of the SMG is largely unknown. Here, we used a mouse model in which the main excretory duct of the SMG is ligated unilaterally to induce inflammation of the gland and examined the expression of Wnt5a, Ror1 and Ror2 genes, encoding Wnt5a ligand and its cognate receptors, which have been implicated in tissue damage or inflammatory responses in variety of tissues. We show that expression levels of Ror1, Ror2, and Wnt5a are increased in the ligated SMG undergoing interstitial fibrosis, which is accompanied by robust expression of fibrosis-associated genes, such as TGF-β1, TNF-α, IL-1β, and MMP-2. Increased immunostaining signal of Ror2 was detected in the fibrotic tissues with abundant accumulation of fibroblasts and collagen fibers in the ligated SMG, suggesting that Ror2-mediated signaling might be activated in response to tissue damage and associated with progression of fibrosis in the SMG.Key words: submandibular gland, Ror2, Wnt5a, fibrosis, inflammation.Entities:
Keywords: Ror2; Wnt5a; fibrosis; inflammation; submandibular gland
Mesh:
Substances:
Year: 2017 PMID: 29070775 DOI: 10.1247/csf.17019
Source DB: PubMed Journal: Cell Struct Funct ISSN: 0386-7196 Impact factor: 2.212