Dental pulp stem cell-derived extracellular matrix: autologous tool boosting bone regeneration

被引:21
作者
Alksne, Milda [1 ]
Kalvaityte, Migle [1 ]
Simoliunas, Egidijus [1 ]
Gendviliene, Ieva [2 ]
Barasa, Povilas [1 ]
Rinkunaite, Ieva [1 ]
Kaupinis, Algirdas [1 ]
Seinin, Dmitrij [3 ]
Rutkunas, Vygandas [2 ]
Bukelskiene, Virginija [1 ]
机构
[1] Vilnius Univ, Inst Biochem, Life Sci Ctr, Vilnius, Lithuania
[2] Vilnius Univ, Inst Odontol, Fac Med, Vilnius, Lithuania
[3] Vilnius Univ Hosp Santaros Klinikos, Natl Ctr Pathol, Vilnius, Lithuania
关键词
bone; bone regeneration; dental pulp stem cell-derived extracellular matrix; dental pulp stem cells; extracellular matrix; OSTEOGENIC DIFFERENTIATION; STROMAL CELLS; IN-VITRO; SCAFFOLDS; PROTEIN; CARTILAGE; ADHESION; PROLIFERATION; ANGIOGENESIS; ANTAGONIST;
D O I
10.1016/j.jcyt.2022.02.002
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Background aims: To facilitate artificial bone construct integration into a patient's body, scaffolds are enriched with different biologically active molecules. Among various scaffold decoration techniques, coating surfaces with cell-derived extracellular matrix (ECM) is a rapidly growing field of research. In this study, for the first time, this technology was applied using primary dental pulp stem cells (DPSCs) and tested for use in artificial bone tissue construction. Methods: Rat DPSCs were grown on three-dimensional-printed porous polylactic acid scaffolds for 7 days. After the predetermined time, samples were decellularized, and the remaining ECM detailed proteomic analysis was performed. Further, DPSC-secreated ECM impact to mesenchymal stromal cells (MSC) behaviour as well as its role in osteoregeneration induction were analysed. Results: It was identified that DPSC-specific ECM protein network ornamenting surface-enhanced MSC attachment, migration and proliferation and even promoted spontaneous stem cell osteogenesis. This protein network also demonstrated angiogenic properties and did not stimulate MSCs to secrete molecules associated with scaffold rejection. With regard to bone defects, DPSC-derived ECM recruited endogenous stem cells, initiating the bone self-healing process. Thus, the DPSC-secreted ECM network was able to significantly enhance artificial bone construct integration and induce successful tissue regeneration. Conclusions: DPSC-derived ECM can be a perfect tool for decoration of various biomaterials in the context of bone tissue engineering. (c) 2022 International Society for Cell & Gene Therapy. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:597 / 607
页数:11
相关论文
共 95 条
[61]   The extracellular matrix: Tools and insights for the "omics" era [J].
Naba, Alexandra ;
Clauser, Karl R. ;
Ding, Huiming ;
Whittaker, Charles A. ;
Carr, Steven A. ;
Hynes, Richard O. .
MATRIX BIOLOGY, 2016, 49 :10-24
[62]   EGFL7: a unique angiogenic signaling factor in vascular development and disease [J].
Nichol, Donna ;
Stuhlmann, Heidi .
BLOOD, 2012, 119 (06) :1345-1352
[63]   Effect of RGD Peptide-Coated TiO2 Nanotubes on the Attachment, Proliferation, and Functionality of Bone-Related Cells [J].
Oh, Seunghan ;
Moon, Kyung Suk ;
Lee, Seoung Hoon .
JOURNAL OF NANOMATERIALS, 2013, 2013
[64]   Decellularized Cell Culture ECMs Act as Cell Differentiation Inducers [J].
Parmaksiz, Mahmut ;
Elcin, Ayse Eser ;
Elcin, Yasar Murat .
STEM CELL REVIEWS AND REPORTS, 2020, 16 (03) :569-584
[65]   Printing three-dimensional tissue analogues with decellularized extracellular matrix bioink [J].
Pati, Falguni ;
Jang, Jinah ;
Ha, Dong-Heon ;
Kim, Sung Won ;
Rhie, Jong-Won ;
Shim, Jin-Hyung ;
Kim, Deok-Ho ;
Cho, Dong-Woo .
NATURE COMMUNICATIONS, 2014, 5
[66]   IL-1 receptor antagonist in metabolic diseases: Dr Jekyll or Mr Hyde? [J].
Perrier, Stephane ;
Darakhshan, Froogh ;
Hajduch, Eric .
FEBS LETTERS, 2006, 580 (27) :6289-6294
[67]   Multipotent mesenchymal stem cells with immunosuppressive activity can be easily isolated from dental pulp [J].
Pierdomenico, L ;
Bonsi, L ;
Calvitti, M ;
Rondelli, D ;
Arpinati, M ;
Chirumbolo, G ;
Becchetti, E ;
Marchionni, C ;
Alviano, F ;
Fossati, V ;
Staffolani, N ;
Franchina, M ;
Grossi, A ;
Bagnara, GP .
TRANSPLANTATION, 2005, 80 (06) :836-842
[68]   Annexin-1-mediated Endothelial Cell Migration and Angiogenesis Are Regulated by Vascular Endothelial Growth Factor (VEGF)-induced Inhibition of miR-196a Expression [J].
Pin, Anne-Laure ;
Houle, Francois ;
Fournier, Patrick ;
Guillonneau, Maeva ;
Paquet, Eric R. ;
Simard, Martin J. ;
Royal, Isabelle ;
Huot, Jacques .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (36) :30541-30551
[69]   Scaffold Design for Bone Regeneration [J].
Polo-Corrales, Liliana ;
Latorre-Esteves, Magda ;
Ramirez-Vick, Jaime E. .
JOURNAL OF NANOSCIENCE AND NANOTECHNOLOGY, 2014, 14 (01) :15-56
[70]   Mechanical signaling through the cytoskeleton regulates cell proliferation by coordinated focal adhesion and Rho GTPase signaling [J].
Provenzano, Paolo P. ;
Keely, Patricia J. .
JOURNAL OF CELL SCIENCE, 2011, 124 (08) :1195-1205