Kwon Seokjun, Ryu Ji Hyun, Kim Junchul, Shin Hyun Ho, Chung Gehoon, Taghizadeh Ali, Lee Jung-Hwan, Kim Jongho, Ku Bon-Cheol, Park Kyungpyo, Lee Sang-Woo
Department of Physiology, School of Dentistry and Dental Research Institute, Seoul National University, Seoul, Republic of Korea.
Department of Biomedical Materials Science, Graduate School of JABA, Department of Carbon Convergence Engineering, Department of Chemical Engineering, Smart Convergence Materials Analysis Center, Wonkwang University, Iksan, Jeonbuk, Republic of Korea.
Biomater Res. 2025 Jul 2;29:0226. doi: 10.34133/bmr.0226. eCollection 2025.
Replacing damaged salivary glands with in vitro-generated artificial glands offers a fundamental solution for salivary gland dysfunction. However, this approach remains challenging due to the gland's complex structure and cellular heterogeneity. Since natural organogenesis of salivary glands successfully orchestrates these complex processes, replicating the developmental niche in vitro is considered a promising solution. However, it consists of complex, branched structures formed by multiple factors; thus, recapitulation of these factors in vitro using a single type of biomaterial is difficult to achieve. Therefore, this study aims to design a scaffold capable of spontaneously mimicking salivary gland's developmental niche. Herein, we demonstrate that catechol-incorporated polyacrylonitrile (PAN-C) nanofiber scaffold spontaneously transforms into biomimetic structures by adsorbing embryonic mesenchyme-derived extracellular matrix (ECM) and growth factors. Accumulated adsorption of ECM and growth factors on PAN-C nanofibers promoted the proliferation, morphogenesis, and functional differentiation of embryonic salivary gland (eSG) organoids in vitro. Transcriptome analysis revealed that the PAN-C nanofiber scaffold effectively reduced mechanical stress-induced gene expression while promoting proliferation and differentiation of salivary gland epithelial cells. In eSG organoids cultured on PAN-C nanofiber scaffolds, the proportion of functional acinar cells expressing apically localized aquaporin-5 was substantially higher than those cultured on polycarbonate membranes, a conventional culture material. Therefore, PAN-C nanofiber scaffolds provide an effective and economical method for generating functional eSG organoids in vitro.
用体外生成的人工腺体替代受损的唾液腺为唾液腺功能障碍提供了一个根本的解决方案。然而,由于腺体结构复杂且细胞具有异质性,这种方法仍然具有挑战性。由于唾液腺的自然器官发生成功地协调了这些复杂的过程,因此在体外复制发育微环境被认为是一个有前景的解决方案。然而,它由多种因素形成的复杂分支结构组成;因此,使用单一类型的生物材料在体外重现这些因素是很难实现的。因此,本研究旨在设计一种能够自发模拟唾液腺发育微环境的支架。在此,我们证明了含儿茶酚的聚丙烯腈(PAN-C)纳米纤维支架通过吸附胚胎间充质来源的细胞外基质(ECM)和生长因子自发转化为仿生结构。ECM和生长因子在PAN-C纳米纤维上的累积吸附促进了胚胎唾液腺(eSG)类器官在体外的增殖、形态发生和功能分化。转录组分析表明,PAN-C纳米纤维支架在促进唾液腺上皮细胞增殖和分化的同时,有效降低了机械应力诱导的基因表达。在PAN-C纳米纤维支架上培养的eSG类器官中,表达顶端定位水通道蛋白-5的功能性腺泡细胞的比例明显高于在传统培养材料聚碳酸酯膜上培养的细胞。因此,PAN-C纳米纤维支架为在体外生成功能性eSG类器官提供了一种有效且经济的方法。