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与现有的 2D 和 3D 模型相比,声悬浮培养的肝球体的功能得到了改善。

Improved functionality of hepatic spheroids cultured in acoustic levitation compared to existing 2D and 3D models.

机构信息

Laboratoire Physique et Mécanique des Milieux Hétérogènes (PMMH), CNRS, ESPCI, 7 Quai Saint-Bernard, 75005, Paris, France.

Inserm U976, CIC-BT CBT501, AP-HP, Université Paris-Cité, Hôpital Saint-Louis, 1 avenue Claude Vellefaux, 75010, Paris, France.

出版信息

Sci Rep. 2024 Sep 14;14(1):21528. doi: 10.1038/s41598-024-72059-x.

Abstract

Hepatic spheroids are of high interest in basic research, drug discovery and cell therapy. Existing methods for spheroid culture present advantages and drawbacks. An alternative technology is explored: the hepatic spheroid formation and culture in an acoustofluidic chip, using HepaRG cell line. Spheroid formation and morphology, cell viability, genetic stability, and hepatic functions are analyzed after 6 days of culture in acoustic levitation. They are compared to 2D culture and non-levitated 3D cultures. Sizes of the 25 spheroids created in a single acoustofluidic microphysiological system are homogeneous. The acoustic parameters in our system do not induce cell mortality nor DNA damage. Spheroids are cohesive and dense. From a functional point of view, hepatic spheroids obtained by acoustic levitation exhibit polarity markers, secrete albumin and express hepatic genes at higher levels compared to 2D and low attachment 3D cultures. In conclusion, this microphysiological system proves not only to be suitable for long-term culture of hepatic spheroids, but also to favor differentiation and functionality within 6 days of culture.

摘要

肝球体在基础研究、药物发现和细胞治疗中具有很高的研究价值。现有的球体培养方法各有优缺点。本研究探索了一种替代技术:使用 HepaRG 细胞系在声悬浮芯片中形成和培养肝球体。在声悬浮培养 6 天后,对球体的形成和形态、细胞活力、遗传稳定性和肝脏功能进行了分析,并与 2D 培养和非悬浮 3D 培养进行了比较。在单个声悬浮微生理系统中形成的 25 个球体的大小均匀。本系统中的声参数不会诱导细胞死亡或 DNA 损伤。球体具有内聚性和高密度。从功能角度来看,与 2D 和低附着 3D 培养相比,通过声悬浮获得的肝球体表现出极性标志物,分泌白蛋白并表达更高水平的肝基因。总之,该微生理系统不仅适合肝球体的长期培养,而且在培养 6 天内还能促进分化和功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa92/11401944/d729b6e972e2/41598_2024_72059_Fig1_HTML.jpg

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