Migration ability and Toll-like receptor expression of human mesenchymal stem cells improves significantly after three-dimensional culture

被引:20
作者
Zhou, Panpan [1 ]
Liu, Zilin [1 ]
Li, Xue [1 ]
Zhang, Bing [1 ]
Wang, Xiaoyuan [1 ]
Lan, Jing [1 ]
Shi, Qing [2 ]
Li, Dong [2 ]
Ju, Xiuli [1 ]
机构
[1] Shandong Univ, Qilu Hosp, Dept Pediat, 107 Wenhuaxilu Rd, Jinan 250012, Shandong, Peoples R China
[2] Shandong Univ, Qilu Hosp, Cryomed Lab, 107 Wenhuaxilu Rd, Jinan 250012, Shandong, Peoples R China
关键词
Mesenchymal stem cell; Three-dimensional culture; Toll-like receptor; C-X-C chemokine receptor type 4; Migratory and homing capacity; BONE-MARROW; STROMAL CELLS; IN-VITRO; IMMUNOMODULATION; DIFFERENTIATION; TISSUE; CD105;
D O I
10.1016/j.bbrc.2017.07.102
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
While the conventional two-dimensional (2D) culture protocol is well accepted for the culture of mesenchymal stem cells (MSCs), this method fails to recapitulate the in vivo native three-dimensional (3D) cellular microenvironment, and may result in phenotypic changes, and homing and migration capacity impairments. MSC preparation in 3D culture systems has been considered an attractive preparatory and delivery method recently. We seeded human umbilical cord-derived MSCs (hUCMSCs) in a 3D culture system with porcine acellular dermal matrix (PADM), and investigated the phenotypic changes, the expression changes of some important receptors, including Toll-like receptors (TLRs) and C-X-C chemokine receptor type 4 (CXCR4) when hUCMSCs were transferred from 2D to 3D systems, as well as the alterations in in vivo homing and migration potential. It was found that the percentage of CD105-positive cells decreased significantly, whereas that of CD34- and CD271-positive cells increased significantly in 3D culture, compared to that in 2D culture. The mRNA and protein expression levels of TLR2, TLR3, TLR4, TLR6, and CXCR4 in hUCMSCs were increased significantly upon culturing with PADM for 3 days, compared to the levels in 2D culture. The numbers of migratory 3D hUCMSCs in the heart, liver, spleen, and bone marrow were significantly greater than the numbers of 2D hUCMSCs, and the worst migration occurred in 3D + AMD3100 (CXCR4 antagonist) hUCMSCs. These results suggested that 3D culture of hUCMSCs with PADM could alter the phenotypic characteristics of hUCMSCs, increase their TLR and CXCR4 expression levels, and promote their migratory and homing capacity in which CXCR4 plays an important role. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:323 / 328
页数:6
相关论文
共 34 条
[1]   CD105 (Endoglin)-Negative Murine Mesenchymal Stromal Cells Define a New Multipotent Subpopulation with Distinct Differentiation and Immunomodulatory Capacities [J].
Anderson, Per ;
Belen Carrillo-Galvez, Ana ;
Garcia-Perez, Angelica ;
Cobo, Marien ;
Martin, Francisco .
PLOS ONE, 2013, 8 (10)
[2]   Adult mesenchymal stem cells: characterization, differentiation, and application in cell and gene therapy [J].
Baksh, D ;
Song, L ;
Tuan, RS .
JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 2004, 8 (03) :301-316
[3]   Concise Review: Bone Marrow-Derived Mesenchymal Stem Cells Change Phenotype Following In Vitro Culture: Implications for Basic Research and the Clinic [J].
Bara, Jennifer J. ;
Richards, R. Geoff ;
Alini, Mauro ;
Stoddart, Martin J. .
STEM CELLS, 2014, 32 (07) :1713-1723
[4]   Isolation and Characterization of Human Mesenchymal Stromal Cell Subpopulations: Comparison of Bone Marrow and Adipose Tissue [J].
Busser, Helene ;
Najar, Mehdi ;
Raicevic, Gordana ;
Pieters, Karlien ;
Pombo, Rafael Velez ;
Philippart, Pierre ;
Meuleman, Nathalie ;
Bron, Dominique ;
Lagneaux, Laurence .
STEM CELLS AND DEVELOPMENT, 2015, 24 (18) :2142-2157
[5]  
Duran R. Cuevas -Diaz, 2013, STEM CELLS INT, V2013
[6]   Dynamic distribution of bone marrow-derived mesenchymal stromal cells and change of pathology after infusing into mdx mice [J].
Feng, S-W ;
Lu, X-L ;
Liu, Z-S ;
Zhang, Y-N ;
Liu, T-Y ;
Li, J-L ;
Yu, M-J ;
Zeng, Y. ;
Zhang, C. .
CYTOTHERAPY, 2008, 10 (03) :254-264
[7]  
Follin B, 2016, TISSUE ENG PART B-RE, V22, P322, DOI [10.1089/ten.TEB.2015.0532, 10.1089/ten.teb.2015.0532]
[8]   Human adipose-derived stromal cells in a clinically applicable injectable alginate hydrogel: Phenotypic and immunomodulatory evaluation [J].
Follin, Bjarke ;
Juhl, Morten ;
Cohen, Smadar ;
Pedersen, Anders Elm ;
Gad, Monika ;
Kastrup, Jens ;
Ekblond, Annette .
CYTOTHERAPY, 2015, 17 (08) :1104-1118
[9]  
Fu J., 2014, PLOS ONE, V9
[10]   Biomaterial-Mesenchymal Stem Cell Constructs for Immunomodulation in Composite Tissue Engineering [J].
Hanson, Summer ;
D'Souza, Rena N. ;
Hematti, Peiman .
TISSUE ENGINEERING PART A, 2014, 20 (15-16) :2162-2168