Avgoustiniatos Efstathios S, Mueller Kate R, Scott Iii William E, Kitzmann Jennifer P, Suszynski Thomas M, Perrault Brian E, Falde Eric J, Balamurugan A N, Hering Bernhard J, Putnam Charles W, Papas Klearchos K
Department of Surgery, Schulze Diabetes Institute, University of Minnesota, Minneapolis, MN, United States.
Department of Surgery, Institute for Cellular Transplantation, University of Arizona, Tucson, AZ, United States.
Front Bioeng Biotechnol. 2024 Jul 11;12:1401608. doi: 10.3389/fbioe.2024.1401608. eCollection 2024.
Conventional culture conditions, such as in T-flasks, require that oxygen diffuse through the medium to reach the islets; in turn, islet surface area density is limited by oxygen availability. To culture a typical clinical islet preparation may require more than 20 T-175 flasks at the standard surface area density of 200 IE/cm. To circumvent this logistical constraint, we tested islets cultured on top of silicon gas-permeable (GP) membranes which place islets in close proximity to ambient oxygen.
Oxygenation of individual islets under three culture conditions, standard low-density, GP high density, and GP high density, were first modeled with finite element simulations. Porcine islets from 30 preparations were cultured for 2 days in devices with GP membrane bottoms or in paired cultures under conventional conditions. Islets were seeded at high density (HD, ∼4000 IE/cm, as measured by DNA) in both GP and GP devices.
In simulations, individual islets under standard culture conditions and high density cultures on GP membranes were both well oxygenated whereas GP high density cultured islets were anoxic. Similarly, compared to the -GP paired controls, islet viability and recovery were significantly increased in HD GP cultures. The diabetes reversal rate in nude diabetic mice was similar for HD GP devices and standard cultures but was minimal with -GP HD cultures.
Culturing islets in GP devices allows for a 20-fold increase of islet surface area density, greatly simplifying the culture process while maintaining islet viability and metabolism.
传统培养条件,如在T型烧瓶中培养,需要氧气透过培养基才能到达胰岛;相应地,胰岛表面积密度受氧气供应限制。以标准表面积密度200 IE/cm培养典型的临床胰岛制剂可能需要20多个T-175烧瓶。为了克服这一后勤限制,我们测试了在硅透气(GP)膜上培养的胰岛,该膜使胰岛与环境氧气紧密接触。
首先用有限元模拟对三种培养条件下(标准低密度、GP高密度和-GP高密度)单个胰岛的氧合情况进行建模。将来自30份制剂的猪胰岛在带有GP膜底部的装置中或在传统条件下的配对培养中培养2天。在GP和-GP装置中均以高密度(HD,通过DNA测量约为4000 IE/cm)接种胰岛。
在模拟中,标准培养条件下的单个胰岛和GP膜上的高密度培养胰岛均氧合良好,而GP高密度培养的胰岛缺氧。同样,与-GP配对对照相比,HD GP培养中的胰岛活力和回收率显著提高。HD GP装置和标准培养中裸鼠糖尿病逆转率相似,但-GP HD培养中则最低。
在GP装置中培养胰岛可使胰岛表面积密度增加20倍,在维持胰岛活力和代谢的同时极大地简化了培养过程。