Kikuchi Kyoko, Sumaru Kimio, Edahiro Jun-Ichi, Ooshima Yuki, Sugiura Shinji, Takagi Toshiyuki, Kanamori Toshiyuki
Research Center of Advanced Bionics, National Institute of Advanced Industrial Science and Technology, Tsukuba Central, Higashi, Ibaraki, Japan.
Biotechnol Bioeng. 2009 Jun 15;103(3):552-61. doi: 10.1002/bit.22253.
Cell micropatterning, a method to place cells at arbitrary regions, is becoming an essential tool to conduct cell biology and tissue engineering. Conventional cell patterning techniques usually allow only single patterning with single cell type on the same culture surface. However, biomedical research today requires even sophisticated fabrication methods that require spatiotemporal control of multiple cell arrangements. Here we introduce in situ cell micropatterning system which enables stepwise cell patterning using a photoresponsive cell culture surface (PRCS) whose cell adhesiveness could be altered by the UV irradiation. To demonstrate an application to tissue engineering, a liver-mimic tissue array was fabricated and liver-specific gene expressions were quantified with real time PCR. Patterned co-culture systems composed of HepG2 spheroids with Balb/3T3 were fabricated, and the optimum spheroid diameter, which yielded the highest cellular functions, was determined to be 150 microm. After 20 days of patterned co-culture of HepG2 spheroids and Balb/3T3, CYP3A4 expression increased 50-fold higher than conventionally cultured HepG2; CYP3A4 expression was 20% higher than randomly co-cultured HepG2 and Balb/3T3. Thus the combination of PRCS and the photomask-free irradiation apparatus showed the versatility of experimental setups and proved to be a powerful tool for biomedical studies.
细胞微图案化,一种将细胞放置在任意区域的方法,正成为进行细胞生物学和组织工程的重要工具。传统的细胞图案化技术通常只允许在同一培养表面上对单一细胞类型进行单次图案化。然而,当今的生物医学研究需要更复杂的制造方法,这些方法需要对多种细胞排列进行时空控制。在这里,我们介绍了一种原位细胞微图案化系统,该系统使用光响应性细胞培养表面(PRCS)实现逐步细胞图案化,其细胞粘附性可通过紫外线照射改变。为了证明其在组织工程中的应用,制作了肝脏模拟组织阵列,并通过实时PCR对肝脏特异性基因表达进行了定量。构建了由HepG2球体与Balb/3T3组成的图案化共培养系统,并确定产生最高细胞功能的最佳球体直径为150微米。在HepG2球体与Balb/3T3进行20天的图案化共培养后,CYP3A4表达比传统培养的HepG2增加了50倍;CYP3A4表达比随机共培养的HepG2和Balb/3T3高20%。因此,PRCS和无光刻掩膜照射装置的组合显示了实验设置的多功能性,并被证明是生物医学研究的有力工具。