Bioprocessing Technology Institute, A*STAR (Agency for Science, Technology and Research), 20 Biopolis Way, #06-01, 138668, Singapore.
Biotechnol Adv. 2013 Nov 15;31(7):1032-46. doi: 10.1016/j.biotechadv.2013.03.006. Epub 2013 Mar 24.
Mesenchymal stem cells (MSCs) have recently made significant progress with multiple clinical trials targeting modulation of immune responses, regeneration of bone, cartilage, myocardia, and diseases like Metachromatic leukodystrophy and Hurler syndrome. On the other hand, the use of human embryonic and induced pluripotent stem cells (hPSCs) in clinical trials is rather limited mainly due to safety issues. Only two clinical trials, retinal pigment epithelial transplantation and treatment of spinal cord injury were reported. Cell doses per treatment can range between 50,000 and 6 billion cells. The current 2-dimensional tissue culture platform can be used when low cell doses are needed and it becomes impractical when doses above 50 million are needed. This demand for future cell therapy has reinvigorated interests in the use of the microcarrier platform for generating stem cells in a scalable 3-dimensional manner. Microcarriers developed for culturing adherent cell lines in suspension have been used mainly in vaccine production and research purposes. Since MSCs grow as monolayers similar to conventional adherent cell lines, adapting MSCs to a microcarrier based expansion platform has been progressing rapidly. On the other hand, establishing a robust microcarrier platform for hPSCs is more challenging as these cells grow in multilayer colonies on extracellular matrices and are more susceptible to shear stress. This review describes properties of commercially available microcarriers developed for cultivation of anchorage dependent cells and present current achievements for expansion and differentiation of stem cells. Key issues such as microcarrier properties and coatings, cell seeding conditions, medium development and improved bioprocess parameters needed for optimal stem cell systems are discussed.
间充质干细胞(MSCs)在调节免疫反应、骨、软骨、心肌再生以及黏脂贮积症和Hurler 综合征等疾病的治疗方面取得了重大进展。另一方面,人胚胎干细胞和诱导多能干细胞(hPSCs)在临床试验中的应用相当有限,主要是由于安全性问题。仅有两项临床试验,即视网膜色素上皮移植和治疗脊髓损伤,被报道。每次治疗的细胞剂量范围在 5 万到 60 亿个细胞之间。当需要低剂量细胞时,可以使用当前的 2 维组织培养平台,但当需要超过 5000 万剂量时,该平台就变得不切实际。这种对未来细胞治疗的需求重新激发了人们对使用微载体平台以可扩展的 3 维方式生成干细胞的兴趣。主要用于悬浮培养贴壁细胞系的微载体已被用于疫苗生产和研究目的。由于 MSCs 像传统的贴壁细胞系一样单层生长,因此将 MSCs 适应于基于微载体的扩增平台的进展非常迅速。另一方面,建立一个用于 hPSCs 的稳健的微载体平台更具挑战性,因为这些细胞在细胞外基质上以多层集落的形式生长,并且更容易受到剪切力的影响。本文综述了为培养锚定依赖性细胞而开发的商业微载体的特性,并介绍了目前在干细胞扩增和分化方面的成就。讨论了微载体特性和涂层、细胞接种条件、培养基开发以及优化干细胞系统所需的改进生物工艺参数等关键问题。