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用于唾液腺组织工程的3D球体培养:成纤维细胞对上皮细胞功能的影响。

3D Spheroid Cultures for Salivary Gland Tissue Engineering: Effects of Fibroblast on Epithelial Cell Function.

作者信息

Nguyen Lan Thi Phuong, Kim Joo Hyun, Son Jiwon, Hur Sung Sik, Lee Minyong, Byeon Hyung Kwon, Kim Jin-Young, Ban Myung Jin, Kim Joo Hyun, Lee Man Ryul, Park Jae Hong, Hwang Yongsung

机构信息

Soonchunhyang Institute of Medi-Bio Science (SIMS), Soonchunhyang University, Cheonan 31151, Republic of Korea.

Department of Integrated Biomedical Science, Soonchunhyang University, Asan 31538, Republic of Korea.

出版信息

Life (Basel). 2025 Apr 5;15(4):607. doi: 10.3390/life15040607.

DOI:10.3390/life15040607
PMID:40283162
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12028948/
Abstract

Three-dimensional (3D) spheroid cultures are crucial for modeling salivary gland (SG) morphogenesis and advancing regenerative medicine. This study evaluated the effects of varying ratios of mouse SG-derived epithelial cells co-cultured with human dermal fibroblasts (hDFs), identifying a 2:1 ratio (spheroids containing 67% EpCAM cells with 33% hDFs) as optimal for preserving native SG-derived epithelial cell phenotypes. At this ratio, 67% EpCAM spheroids maintained structural integrity and demonstrated a significant reduction in apoptosis and senescence markers, specifically, cleaved caspase-3 (Cc3) and Serpine1, alongside an enhanced expression of the progenitor marker Keratin 5 (KRT5). This highlights the pivotal role of fibroblasts in supporting epithelial cell function in 3D cultures. These spheroids provide a useful model for developing SG tissues that closely mimic physiological properties. Despite promising results, these findings are preliminary and require further validation under diverse conditions and across different SG models.

摘要

三维(3D)球体培养对于唾液腺(SG)形态发生建模和推进再生医学至关重要。本研究评估了小鼠SG来源的上皮细胞与人真皮成纤维细胞(hDFs)以不同比例共培养的效果,确定2:1的比例(球体含有67%的EpCAM细胞和33%的hDFs)最适合保留天然SG来源的上皮细胞表型。在此比例下,67% EpCAM球体保持结构完整性,并显示凋亡和衰老标志物(特别是裂解的半胱天冬酶-3(Cc3)和丝氨酸蛋白酶抑制剂1)显著减少,同时祖细胞标志物角蛋白5(KRT5)的表达增强。这突出了成纤维细胞在支持3D培养中上皮细胞功能方面的关键作用。这些球体为开发紧密模拟生理特性的SG组织提供了有用的模型。尽管结果很有前景,但这些发现是初步的,需要在不同条件下和不同SG模型中进一步验证。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e99/12028948/24821a48d40b/life-15-00607-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e99/12028948/e029c894a5b1/life-15-00607-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e99/12028948/16c705c1b44f/life-15-00607-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e99/12028948/24821a48d40b/life-15-00607-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e99/12028948/e029c894a5b1/life-15-00607-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e99/12028948/16c705c1b44f/life-15-00607-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5e99/12028948/24821a48d40b/life-15-00607-g003.jpg

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本文引用的文献

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PIEZO1 activation may serve as an early tissue biomarker for the prediction of irradiation-induced salivary gland dysfunction.机械敏感离子通道蛋白 1(PIEZO1)的激活可作为预测放射性唾液腺损伤的早期组织生物标志物。
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Mesenchymal Stem Cell Spheroids: A Promising Tool for Vascularized Tissue Regeneration.
间质干细胞球:用于血管化组织再生的有前途的工具。
Tissue Eng Regen Med. 2024 Jul;21(5):673-693. doi: 10.1007/s13770-024-00636-2. Epub 2024 Apr 5.
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Exploring the Cocktail Factor Approach to Generate Salivary Gland Progenitors through Co-Culture Techniques.探索鸡尾酒因子方法通过共培养技术生成唾液腺祖细胞。
Tissue Eng Regen Med. 2024 Jul;21(5):749-759. doi: 10.1007/s13770-024-00632-6. Epub 2024 Mar 11.
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Fibroblast-Epithelium Co-culture Methods Using Epithelial Organoids and Cell Line-Derived Spheroids.成纤维细胞-上皮细胞共培养方法:使用上皮类器官和细胞系衍生的球体。
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Cell Surface Modification-Mediated Primary Intestinal Epithelial Cell Culture Platforms for Assessing Host-Microbiota Interactions.用于评估宿主-微生物群相互作用的细胞表面修饰介导的原代肠上皮细胞培养平台
Biomater Res. 2024 Jan 25;28:0004. doi: 10.34133/bmr.0004. eCollection 2024.
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Salivary gland regeneration: from salivary gland stem cells to three-dimensional bioprinting.唾液腺再生:从唾液腺干细胞到三维生物打印。
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