Comparative evaluation of morphology and osteogenic behavior of human Wharton's jelly mesenchymal stem cells on 2D culture plate and 3D biomimetic scaffold

被引:11
作者
Jamalpoor, Zahra [1 ]
Soleimani, Mansoureh [2 ,3 ]
Taromi, Nafise [2 ,4 ]
Asgari, Alireza [5 ]
机构
[1] Aja Univ Med Sci, Trauma Res Ctr, Tehran, Iran
[2] Iran Univ Med Sci, Cellular & Mol Res Ctr, Tehran, Iran
[3] Iran Univ Med Sci, Dept Anat, Tehran, Iran
[4] Iran Univ Med Sci, Fac Allied Med, Dept Med Biotechnol, Tehran, Iran
[5] Aja Univ Med Sci, Aerosp Med Res Ctr, Tehran, Iran
基金
美国国家科学基金会;
关键词
2D culture plate; 3D scaffold; bone tissue engineering; human Wharton's jelly; mesenchymal stem cells; UMBILICAL-CORD; BONE-MARROW; IN-VITRO; BIOCOMPOSITE SCAFFOLD; ENDOTHELIAL-CELLS; DIFFERENTIATION; CHITOSAN; FABRICATION; PROLIFERATION; MICROCARRIERS;
D O I
10.1002/jcp.28876
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Expansion of seeded human Wharton's jelly mesenchymal stem cells (hWJ-MSCs) on 2D culture plates and 3D nano-hydroxyapatite/chitosan/gelatin scaffolds, from morphology and osteoactivity points of view, were investigated. Cell attachment and spreading, temporal expression profiles of selected osteogenic gene and protein markers, intracellular alkaline phosphatase enzyme activity (ALP activity), and matrix mineralization were assayed over the course of the experiments. Morphological results demonstrated hWJ-MSCs had greater affinity to adhere onto the 3D scaffold surface, as the number and thickness of the filopodia were higher in the 3D compared with 2D culture system. Functionally, the intracellular ALP activity and extracellular mineralization in 3D scaffolds were significantly greater, in parallel with elevation of osteogenic markers at the mRNA and protein levels at all-time point. It is concluded that 3D scaffolds, more so than 2D culture plate, promote morphology and osteogenic behavior of WJ-MSCs in vitro, a promising system for MSCs expansion without compromising their stemness before clinical transplantation.
引用
收藏
页码:23123 / 23134
页数:12
相关论文
共 57 条
[1]  
Ansari A. S., 2018, STEM CELLS INT, V9, P2018
[2]   Different Porosities of Chitosan Can Influence the Osteogenic Differentiation Potential of Stem Cells [J].
Ardeshirylajimi, Abdolreza ;
Delgoshaie, Mahdieh ;
Mirzaei, Samaneh ;
Khojasteh, Arash .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2018, 119 (01) :625-633
[3]   Deconstructing the third dimension - how 3D culture microenvironments alter cellular cues [J].
Baker, Brendon M. ;
Chen, Christopher S. .
JOURNAL OF CELL SCIENCE, 2012, 125 (13) :3015-3024
[4]   Osteogenic differentiation of Wharton's jelly-derived mesenchymal stem cells cultured on WJ-scaffold through conventional signalling mechanism [J].
Beiki, Bahareh ;
Zeynali, Bahman ;
Taghiabadi, Ehsan ;
Seyedjafari, Ehsan ;
Kehtari, Mousa .
ARTIFICIAL CELLS NANOMEDICINE AND BIOTECHNOLOGY, 2018, 46 :S1032-S1042
[5]   Cell viability assessment using the Alamar blue assay: A comparison of 2D and 3D cell culture models [J].
Bonnier, F. ;
Keating, M. E. ;
Wrobel, T. P. ;
Majzner, K. ;
Baranska, M. ;
Garcia-Munoz, A. ;
Blanco, A. ;
Byrne, H. J. .
TOXICOLOGY IN VITRO, 2015, 29 (01) :124-131
[6]   The role of pharmacologically active microcarriers releasing TGF-β3 in cartilage formation in vivo by mesenchymal stem cells [J].
Bouffi, Carine ;
Thomas, Olivier ;
Bony, Claire ;
Giteau, Alexandra ;
Venier-Julienne, Marie-Claire ;
Jorgensen, Christian ;
Montero-Menei, Claudia ;
Noel, Daniele .
BIOMATERIALS, 2010, 31 (25) :6485-6493
[7]   Umbilical cord mesenchymal stromal cell transplantations: A systemic analysis of clinical trials [J].
Can, Alp ;
Celikkan, Ferda Topal ;
Cinar, Ozgur .
CYTOTHERAPY, 2017, 19 (12) :1351-1382
[8]  
Chang HI, 2011, REGENERATIVE MEDICINE AND TISSUE ENGINEERING - CELLS AND BIOMATERIALS, P569
[9]   Application of human mesenchymal and pluripotent stem cell microcarrier cultures in cellular therapy: Achievements and future direction [J].
Chen, Allen Kuan-Liang ;
Reuveny, Shaul ;
Oh, Steve Kah Weng .
BIOTECHNOLOGY ADVANCES, 2013, 31 (07) :1032-1046
[10]  
Chen WC, 2013, TISSUE ENG PT A, V19, P915, DOI [10.1089/ten.tea.2012.0172, 10.1089/ten.TEA.2012.0172]