组织工程与重建外科杂志 ›› 2015, Vol. 11 ›› Issue (4): 239-245.doi: 10.3969/j.issn.1673-0364.2015.04.005

• 论著 • 上一篇    下一篇

利用PDMS微孔阵列微型反应器设计hADSCs空间堆叠模型

何懿,栾杰   

  1. 中国医学科学院整形外科医院乳房整形及再造中心
  • 发布日期:2020-07-23

The Designing of hADSCs Stacking Model by Utilizing PDMS Microwell Micro-reactor

HE Yi,LUAN Jie   

  • Published:2020-07-23

摘要: 目的 利用微尺度技术(Micro-scale technologies)建立人脂肪干细胞(h ADSCs)体外三维培养平台,观察空间堆叠状态对种植后的h ADSCs增殖和凋亡的影响。方法 利用光刻技术在硅晶元表面生成直径60μm、80μm、100μm和150μm的微柱状结构,经聚二甲基硅氧烷(PDMS)倒模、固化生成同规格的微孔阵列(Micro-well arrays),加装PDMS环形外壁后组成微型反应器,测量、分析此实验平台的加工误差率;第3代h ADSCs配制成1×105cells/m L、6×104cells/m L、3×104cells/m L三种浓度单细胞悬液,并各取200μL分别接种于纯平PDMS微型反应器及直径60μm、80μm、100μm和150μm微孔微型反应器内,选择种植后24 h、72 h、120 h和168 h为采样点,对各观察组细胞分布状况进行形态学描述、细胞计数及活/死细胞检测。结果 各孔径PDMS微孔阵列的微孔口径精度误差率均不超过0.2%;档h ADSCs以6×104cells/m L浓度接种时,细胞基本可以实现在150μm微孔内呈单层平铺、100μm微孔内呈2层堆叠、80μm微孔内呈3层堆叠;各微孔内细胞数在7 d内均无明显的数量变化,60μm组微孔内细胞数最少且微孔外平面残留细胞最多(P<0.05);60μm组微孔内凋亡细胞比例高于其他组(P<0.05)。结论 微加工倒模制作的PDMS微孔阵列培养平台误差率低,可满足高精度设计需要;h ADSCs短时间(7 d)接种于微孔内处于增殖静止状态,能够保持三维堆叠状态稳定,便于进行堆叠状态下的细胞学早期研究;h ADSCs在不同口径微孔内可以实现不同的堆叠层数,其凋亡比率与堆叠层数有关,堆叠层数少的细胞凋亡比例低于堆叠层数多者。

关键词: 微孔阵列, 微尺度技术, 聚二甲基硅氧烷, 人脂肪干细胞

Abstract: Objective To establish a three-dimensional cultivation platform for human adipose derived stem cells (hADSCs) by utilizing micro-scale technology, and to explore the influence of three-dimensional stacking condition to cell proliferation and apoptosis. Methods Micro-columnar structure were generated by micro-scale technology on silicon master with diameter of 60 μm, 80 μm, 100 μm and 150 μm respectively. The same specification micro-well arrays were acquired by reversing mould aperture using polydimethylsiloxane (PDMS), which equipped with PDMS ring on the outer wall to constitute micro-reactor. The error rate of this platform was analyzed. Then the third generation of human adipose-derived stem cells (hADSCs) were selected and mixed into single cell suspension mixture with three kinds of concentration, including 3×104 cells/mL, 6×104 cells/mL and 1×105 cells/mL. And 200μL cell suspension was injected into micro-reactor to establish three-dimensional culture models with different stacked layers. Then 24 hours, 72 hours, 120 hours and 168 hours were choosed as sample collection time point. The morphology description of cell distribution in each group was analyzed with scanning electron microscopy, the arrangement inside the microwells and the cell distribution outside the microwells were described, and the live/dead cells were counted and tested in each aperture and micro hole by using laser scanning confocal microscope. Results The error rate of diameter and pore diameter were no more than 0.2%. When hADSCs were planted by the density of 6 ×104 cells/mL, the stacking layer condition can be acquired. The number of cell within microwells was at static condition no more than 7 days. The 60 μm group had the highest number of out-of-well cell (P<0.05) and lowest 05). The highest apoptosis ratio was also observed in the 60 μm group (P<0.05). Conclusion The application of microscale technique can acquire extremely low error rate, which can satisfy the requirements of high precision design. The static proliferation condition of planted hADSCs can be maintained within microwells, which can stabilize the condition of cells and be designed as a perfect three dimention model for cell research at early stage of plant. The stackable condition of hADSCs can be acquired by planting into microwells with different diameters, which can significant affect the rate of apoptosis under this three dimentional cultivate condition. Thinner layer of stack may reduce the rate of apoptosis.

Key words: Micro-well arrays, Micro-scale technology, Polydimethylsiloxane, Human adipose tissue derived stem cells

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