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Immortalization of Salivary Gland Epithelial Cells of Xerostomic Patients: Establishment and Characterization of Novel Cell Lines

机译:挠性症患者唾液腺上皮细胞的永生化:建立和表征新细胞系

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摘要

Primary Sjögren’s Syndrome (pSS) is an autoimmune disease mainly affecting salivary and lacrimal glands. Previous pSS studies have relied on primary cell culture models or cancer cell lines with limited relevance to the disease. Our objective was to generate and characterize immortalized salivary gland epithelial cells (iSGECs) derived from labial salivary gland (LSG) biopsies of pSS patients (focus score > 1) and non-Sjögren’s Syndrome (nSS) xerostomic (i.e., sicca) female patients. To characterize iSGECs (n = 3), mRNA expression of specific epithelial and acinar cell markers was quantified by qRT-PCR. Protein expression of characterization markers was determined by immunocytochemistry and Western blot. Secretion of α-amylase by iSGECs was confirmed through colorimetric activity assay. Spheroid formation and associated alterations in expression markers were determined using matrigel-coated cell culture plates. Consistent mRNA and protein expressions of both epithelial and pro-acinar cell markers were observed in all three iSGEC lines. When cultured on matrigel medium, iSGECs formed spheroids, secreted α-amylase after β-adrenergic stimulation, and expressed multiple acinar cell markers at late passages. One iSGEC line retained adequate cell morphology without a loss of SV40Lt expression and proliferation potential after over 100 passages. In conclusion, our established iSGEC lines represent a viable model for salivary research due to their passaging capacity and maintenance of pro-acinar cell characteristics.
机译:原发性Sjögren的综合征(PSS)是一种主要影响唾液和泪腺的自身免疫性疾病。以前的PSS研究依赖于原发性细胞培养模型或癌细胞系与疾病有限。我们的目的是产生和表征衍生自PSS患者的唇唾液腺(LSG)活组织检查的永生唾液腺上皮细胞(ISGEC)(焦点评分> 1)和非Sjögren的综合征(NSS)Xerostomic(即Sicca)女性患者。为了表征Isgecs(n = 3),通过QRT-PCR定量特定上皮和缩醛细胞标记物的mRNA表达。通过免疫细胞化学和Western印迹测定表征标志物的蛋白质表达。通过比色活性测定证实了ISGEC的α-淀粉酶的分泌。使用基质涂覆的细胞培养板测定表达标记中的球形形成和相关的改变。在所有三种ISGEC线中观察到上皮细胞和Pro-aciNAR细胞标记物的一致mRNA和蛋白质表达。当在Matrigel培养基上培养时,在β-肾上腺素能刺激后形成的α-淀粉酶分泌α-淀粉酶,并在晚期通道中表达多个缩醛细胞标记物。一个ISGEC线保留了足够的细胞形态,而在100多个通道之后,没有SV40LT表达和增殖潜力的损失。总之,我们已建立的ISGEC线代表了一种可行的唾液研究模型,因为它们的传递能力和维持副缩醛细胞特征。

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