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单细胞 RNA 测序分析鉴定出血管紧张素原和甘丙肽是小鼠唾液腺腺泡细胞的独特分子标记物。

Single-Cell RNA-Seq Analysis Identifies Angiotensinogen and Galanin as Unique Molecular Markers of Acinar Cells in Murine Salivary Glands.

机构信息

Chongqing Key Laboratory of Oral Diseases and Biomedical Sciences, and Stomatological Hospital of Chongqing Medical University, Chongqing, China.

Department of Endodontics, Stomatological Hospital of Chongqing Medical University, Chongqing, China.

出版信息

Stem Cells Dev. 2023 Dec;32(23-24):758-767. doi: 10.1089/scd.2023.0125. Epub 2023 Nov 16.

DOI:10.1089/scd.2023.0125
PMID:37823745
Abstract

The submandibular gland (SMG) and sublingual gland (SLG) are two of three major salivary glands in mammals and comprise serous and mucous acinar cells. The two glands share some functional properties, which are largely dependent on the types of acinar cells. In recent years, while ScRNA-seq (single-cell sequencing) with a 10 × platform has been used to explore molecular markers in salivary glands, few studies have examined the acinar heterogeneity and unique molecular markers between SMG and SLG. This study aimed to identify the molecular markers of acinar cells in the SLG and SMG. We performed ScRNA-seq analyses in 4-week-old mice and verified the screened molecular markers using reverse transcription-quantitative real-time PCR, immunohistochemistry, and immunofluorescence. Our results showed prominently heterogeneous acinar cells, although there was great similarity in the cluster composition between the two glands at 4 weeks. Furthermore, we demonstrated that is a specific marker of SMG serous acinar cells, whereas is a specific marker of SLG mucous acinar cells. Trajectory inference revealed that and represent two types of differential acinar cell clusters during late development in adults. Thus, we reveal previously unknown specific markers for salivary acinar cell diversity, which has extensive implications for their further functional research.

摘要

下颌下腺 (SMG) 和舌下腺 (SLG) 是哺乳动物的三大唾液腺中的两个,由浆液细胞和黏液细胞组成。这两个腺体具有一些共同的功能特性,这些特性在很大程度上取决于腺泡细胞的类型。近年来,虽然使用 10× 平台的单细胞测序 (scRNA-seq) 来探索唾液腺中的分子标记物,但很少有研究探讨 SMG 和 SLG 之间的腺泡异质性和独特的分子标记物。本研究旨在鉴定 SLG 和 SMG 腺泡细胞的分子标记物。我们对 4 周龄的小鼠进行了 scRNA-seq 分析,并使用逆转录定量实时 PCR、免疫组织化学和免疫荧光验证了筛选出的分子标记物。我们的结果表明,尽管在 4 周时,两个腺体的聚类组成非常相似,但仍存在明显的腺泡细胞异质性。此外,我们证明 是 SMG 浆液性腺泡细胞的特异性标记物,而 是 SLG 黏液性腺泡细胞的特异性标记物。轨迹推断表明 和 代表了成年后期发育过程中两种不同的腺泡细胞簇。因此,我们揭示了唾液腺腺泡细胞多样性的先前未知的特异性标记物,这对它们的进一步功能研究具有广泛的意义。

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