Suppr超能文献

梅奥诊所唾液组织类器官生物样本库:唾液再生研究的资源

The Mayo Clinic Salivary Tissue-Organoid Biobanking: A Resource for Salivary Regeneration Research.

作者信息

Aalam Syed Mohammed Musheer, Varela Ana Rita, Khaderi Aalim, Mondesir Ronsard J, Mun Dong-Gi, Ding Andrew, Lombaert Isabelle M A, Coppes Rob P, Emperumal Chitra Priya, Pandey Akhilesh, Janus Jeffrey R, Kannan Nagarajan

机构信息

Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, USA.

Biologic and Materials Sciences and Prosthodontics, University of Michigan School of Dentistry, 1011 N. University Ave, Ann Arbor, MI, USA.

出版信息

bioRxiv. 2024 Feb 27:2024.02.23.581761. doi: 10.1101/2024.02.23.581761.

Abstract

The salivary gland (SG) is an essential organ that secretes saliva, which supports versatile oral function throughout life, and is maintained by elusive epithelial stem and progenitor cells (SGSPC). Unfortunately, aging, drugs, autoimmune disorders, and cancer treatments can lead to salivary dysfunction and associated health consequences. Despite many ongoing therapeutic efforts to mediate those conditions, investigating human SGSPC is challenging due to lack of standardized tissue collection, limited tissue access, and inadequate purification methods. Herein, we established a diverse and clinically annotated salivary regenerative biobanking at the Mayo Clinic, optimizing viable salivary cell isolation and clonal assays in both 2D and 3D-matrigel growth environments. Our analysis identified ductal epithelial cells in vitro enriched with SGSPC expressing the CD24/EpCAM/CD49f+ and PSMA- phenotype. We identified PSMA expression as a reliable SGSPC differentiation marker. Moreover, we identified progenitor cell types with shared phenotypes exhibiting three distinct clonal patterns of salivary differentiation in a 2D environment. Leveraging innovative label-free unbiased LC-MS/MS-based single-cell proteomics, we identified 819 proteins across 71 single cell proteome datasets from purified progenitor-enriched parotid gland (PG) and sub-mandibular gland (SMG) cultures. We identified distinctive co-expression of proteins, such as KRT1/5/13/14/15/17/23/76 and 79, exclusively observed in rare, scattered salivary ductal basal cells, indicating the potential de novo source of SGSPC. We also identified an entire class of peroxiredoxin peroxidases, enriched in PG than SMG, and attendant HO-dependent cell proliferation in vitro suggesting a potential role for PRDX-dependent floodgate oxidative signaling in salivary homeostasis. The distinctive clinical resources and research insights presented here offer a foundation for exploring personalized regenerative medicine.

摘要

唾液腺(SG)是一种分泌唾液的重要器官,唾液在人的一生中支持多种口腔功能,并且由难以捉摸的上皮干细胞和祖细胞(SGSPC)维持。不幸的是,衰老、药物、自身免疫性疾病和癌症治疗会导致唾液功能障碍及相关健康问题。尽管目前正在进行许多治疗这些病症的努力,但由于缺乏标准化的组织采集、有限的组织获取途径和不完善的纯化方法,研究人类SGSPC具有挑战性。在此,我们在梅奥诊所建立了一个多样化且具有临床注释的唾液再生生物样本库,优化了在二维和三维基质胶生长环境中的活唾液细胞分离和克隆分析。我们的分析在体外鉴定出富含表达CD24/EpCAM/CD49f+和PSMA-表型的SGSPC的导管上皮细胞。我们确定PSMA表达是一种可靠的SGSPC分化标志物。此外,我们在二维环境中鉴定出具有共同表型的祖细胞类型,它们呈现出三种不同的唾液分化克隆模式。利用基于无标记、无偏倚的液相色谱-质谱联用(LC-MS/MS)的创新单细胞蛋白质组学技术,我们从纯化的富含祖细胞的腮腺(PG)和下颌下腺(SMG)培养物的71个单细胞蛋白质组数据集中鉴定出819种蛋白质。我们鉴定出蛋白质的独特共表达,如KRT1/5/13/14/15/17/23/76和79,仅在罕见的散在唾液导管基底细胞中观察到,这表明SGSPC可能有新生来源。我们还鉴定出一类过氧化物酶,在PG中比在SMG中更丰富,并且体外伴随HO依赖性细胞增殖,这表明PRDX依赖性闸门氧化信号在唾液稳态中可能发挥作用。这里呈现的独特临床资源和研究见解为探索个性化再生医学提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/660a/10925098/7941600302af/nihpp-2024.02.23.581761v1-f0001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验