Abstract

ObjectiveA major characteristic of the autoimmune disease primary Sjögren's syndrome (SS) is salivary gland (SG) hypofunction. The inability of resident SG stem cells (SGSCs) to maintain homeostasis and saliva production has never been explained and limits our comprehension of mechanisms underlying primary SS. The present study was undertaken to investigate the role of salivary gland stem cells in hyposalivation in primary SS.Methods SGSCs were isolated from parotid biopsy samples from controls and patients classified as having primary SS or incomplete primary SS, according to the American College of Rheumatology/European League Against Rheumatism criteria. Self‐renewal and differentiation assays were used to determine SGSC regenerative potential, RNA was extracted for sequencing analysis, single telomere length analysis was conducted to determine telomere length, and frozen tissue samples were used for immunohistochemical analysis.Results SGSCs isolated from primary SS parotid gland biopsy samples were regeneratively inferior to healthy control specimens. We demonstrated that SGSCs from samples from patients with primary SS are not only lower in number and less able to differentiate, but are likely to be senescent, as revealed by telomere length analysis, RNA sequencing, and immunostaining. We further found that SGSCs exposed to primary SS–associated proinflammatory cytokines we induced to proliferate, express senescence‐associated genes, and subsequently differentiate into intercalated duct cells. We also localized p16+ senescent cells to the intercalated ducts in primary SS SG tissue, suggesting a block in SGSC differentiation into acinar cells.ConclusionThis study represents the first characterization of SGSCs in primary SS, and also the first demonstration of a linkage between an autoimmune disease and a parenchymal premature‐aging phenotype. The knowledge garnered in this study indicates that disease‐modifying antirheumatic drugs used to treat primary SS are not likely to restore saliva production, and should be supplemented with fresh SGSCs to recover saliva production.

Highlights

  • We began by isolating salivary gland stem cell (SGSC) from parotid salivary gland (SG) biopsies of control patients with healthy SGs (HCs) and primary Sjögren’s syndrome (pSS) patients fulfilling the ACR-EULAR classification criteria 20

  • SGSCs are initially cultured from processed biopsies as primary spheres, in Wnt-containing medium

  • SGSCs are epithelial cell adhesion molecule (EpCAM)hi in nature. The number of both spheres generated per EpCAMhi cell and yield of spheres per mg of biopsy was significantly lower (10 fold difference) from biopsies from pSS patients compared to

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Summary

Methods

SGSCs were isolated from parotid biopsies of controls and patients classified as pSS or incomplete pSS, according to ACR-EULAR criteria. Parotid SG tissue was obtained from donors (after informed consent and IRB approval (METC2016/010) who were treated for a squamous cell carcinoma of the oral cavity. In these patients an elective head and neck dissection procedure was performed. During this procedure parotid SG is exposed and removed as part of the dissection procedure This tissue does not contain malignant cells, as oral squamous cell carcinoma does not disseminate to the parotid salivary gland. All patients gave IRB consent and approval (METc 2016/010)

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