Co-culture of smooth muscle cells and endothelial cells on three-dimensional bioprinted polycaprolactone scaffolds for cavernosal tissue engineering

被引:5
|
作者
Oh, Kyung-Jin [1 ]
Yu, Ho Song [1 ,2 ]
Park, Jinju [2 ]
Lee, Hyun-Suk [2 ]
Park, Su A. [3 ]
Park, Kwangsung [1 ]
机构
[1] Chonnam Natl Univ, Sch Med, Dept Urol, Gwangju 501757, South Korea
[2] Chonnam Natl Univ, Sexual Med Res Ctr, Gwangju, South Korea
[3] KIMM, Nano Convergence & Mfg Syst Res Div, 104 Sinseongno, Daejeon, South Korea
来源
AGING MALE | 2020年 / 23卷 / 05期
关键词
3D bioprinting; tissue engineering; smooth muscle; endothelial cell; CORPUS CAVERNOSUM; CORPORAL TISSUE; IN-VITRO; RECONSTITUTION; CONSTRUCTION; ACTIVATION; ADHESION; MODEL;
D O I
10.1080/13685538.2019.1601175
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose: In vitro evaluation of polycaprolactone (PCL) scaffolds fabricated by a three-dimensional (3D) printing technique for tissue engineering applications in the corpus cavernosum. Materials and methods: PCL scaffolds were fabricated by use of a 3 D bioprinting system. The 3D-printed scaffolds had interconnected structures for cell ingrowth. Human aortic smooth muscle cells (haSMCs) were seeded on the scaffold and cultured for 5 days, and then human umbilical vein endothelial cells (HUVECs) were also added on the scaffolds and co-cultured with haSMCs for up to 7 days. The ability of these scaffolds to support the growth of HUVECs and haSMCs was investigated in vitro. 3 D strand-deposited scaffolds were characterized by scanning electron microscopy (SEM) images and porosity measurement. Results: SEM images showed the surface of the PCL scaffolds to be well covered by HUVECs and haSMCs. Immunofluorescent staining of alpha-flk1 and alpha-smooth muscle actin on the HUVECs and haSMCs seeded scaffolds confirmed that the cells remained viable and proliferated throughout the time course of the culture. Conclusion: 3 D bioprinting of a PCL scaffold is feasible for co-culturing of HUVECs and haSMCs. This was a preliminary study to investigate the possibility of fabrication of tissue-engineered corpus cavernosum.
引用
收藏
页码:830 / 835
页数:6
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