Decellularized Swine Dental Pulp Tissue for Regenerative Root Canal Therapy

被引:61
作者
Alqahtani, Q. [1 ]
Zaky, S. H. [1 ,2 ,3 ]
Patil, A. [1 ]
Beniash, E. [1 ,3 ,4 ]
Ray, H. [1 ,4 ,5 ]
Sfeir, C. [1 ,3 ,4 ]
机构
[1] Univ Pittsburgh, Sch Dent Med, Ctr Craniofacial Regenerat, Pittsburgh, PA USA
[2] Univ Pittsburgh, Sch Dent Med, Dept Restorat Dent, Pittsburgh, PA USA
[3] Univ Pittsburgh, Sch Dent Med, Dept Oral Biol, Pittsburgh, PA USA
[4] Univ Pittsburgh, McGowan Inst Regenerat Med, Pittsburgh, PA USA
[5] Univ Pittsburgh, Sch Dent Med, Dept Endodont, Pittsburgh, PA USA
关键词
extracellular matrix (ECM); regeneration; pulp biology; cell differentiation; tissue engineering; bioengineering; EXTRACELLULAR-MATRIX; BIOLOGIC SCAFFOLD; ENDODONTIC TREATMENT; GROWTH-FACTORS; STEM-CELLS; PORCINE;
D O I
10.1177/0022034518785124
中图分类号
R78 [口腔科学];
学科分类号
100302 [口腔临床医学];
摘要
In the current theme of dental pulp regeneration, biological and synthetic scaffolds are becoming a potential therapy for pulp revitalization. The goal is to provide a suitable environment for cellular infiltration, proliferation, and differentiation. The extracellular matrix (ECM) represents a natural scaffold material resembling the native tissue chemical and mechanical properties. In the past few years, ECM-based scaffolds have shown promising results in terms of progenitor cells recruitment, promotion of constructive remodeling, and modulation of host response. These properties make ECM-derived scaffolds an ideal candidate for pulp regenerative therapy. Development of strategies for clinically relevant tissue engineering using dental pulp extracellular matrix (DP-ECM) can provide an alternative to conventional root canal treatment. In this work, we successfully decellularized ECM derived from porcine dental pulp. The resulting scaffold was characterized using immunostaining (collagen type I, dentin matrix protein 1, dentin sialoprotein, and Von Willebrand factor) and enzyme-linked immunosorbent assay (transforming growth factor beta, vascular endothelial growth factor, and basic fibroblast growth factor) for extracellular proteins where the ECM retained its proteins and significant amount of growth factors. Furthermore, a pilot in vivo study was conducted where the matrix was implanted for 8 wk in a dog root canal model. Our in vitro and preliminary in vivo data show that the decellularized ECM supports cellular infiltration together with the expression of pulp-dentin and vascular markers (DSP and CD31) compared to the controls. Herein, we show the feasibility to produce a decellularized ECM scaffold and validate the concept of using ECM-based scaffolds for pulp regeneration.
引用
收藏
页码:1460 / 1467
页数:8
相关论文
共 40 条
[1]
Epimorphic regeneration approach to tissue replacement in adult mammals [J].
Agrawal, Vineet ;
Johnson, Scott A. ;
Reing, Janet ;
Zhang, Li ;
Tottey, Stephen ;
Wang, Gang ;
Hirschi, Karen K. ;
Braunhut, Susan ;
Gudas, Lorraine J. ;
Badylak, Stephen F. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (08) :3351-3355
[2]
Whole-Organ Tissue Engineering: Decellularization and Recellularization of Three-Dimensional Matrix Scaffolds [J].
Badylak, Stephen F. ;
Taylor, Doris ;
Uygun, Korkut .
ANNUAL REVIEW OF BIOMEDICAL ENGINEERING, VOL 13, 2011, 13 :27-53
[3]
Possible role of DMP1 in dentin mineralization [J].
Beniash, Elia ;
Deshpande, Atul S. ;
Fang, Ping An ;
Lieb, Nicholas S. ;
Zhang, Xiaoyuan ;
Sfeir, Charles S. .
JOURNAL OF STRUCTURAL BIOLOGY, 2011, 174 (01) :100-106
[4]
Role of synthetic extracellular matrix in development of engineered dental pulp [J].
Bohl, KS ;
Shon, J ;
Rutherford, B ;
Mooney, DJ .
JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1998, 9 (07) :749-764
[5]
Chronic Inflammation and Angiogenic Signaling Axis Impairs Differentiation of Dental-Pulp Stem Cells [J].
Boyle, Michael ;
Chun, Crystal ;
Strojny, Chelsee ;
Narayanan, Raghuvaran ;
Bartholomew, Amelia ;
Sundivakkam, Premanand ;
Alapati, Satish .
PLOS ONE, 2014, 9 (11)
[6]
Brown BN, 2011, TISSUE ENG PART C-ME, V17, P411, DOI 10.1089/ten.TEC.2010.0342
[7]
In vivo degradation of 14C-labeled porcine dermis biologic scaffold [J].
Carey, Lisa E. ;
Dearth, Christopher L. ;
Johnson, Scott A. ;
Londono, Ricardo ;
Medberry, Christopher J. ;
Daly, Kerry A. ;
Badylak, Stephen E. .
BIOMATERIALS, 2014, 35 (29) :8297-8304
[8]
Preparation and rheological characterization of a gel form of the porcine urinary bladder matrix [J].
Freytes, Donald O. ;
Martin, Jeffrey ;
Velankar, Sachin S. ;
Lee, Annie S. ;
Badylak, Stephen F. .
BIOMATERIALS, 2008, 29 (11) :1630-1637
[9]
Friedman Shimon, 2004, J Calif Dent Assoc, V32, P493
[10]
Cell-free Approaches for Dental Pulp Tissue Engineering [J].
Galler, Kerstin M. ;
Eidt, Andreas ;
Schmalz, Gottfried .
JOURNAL OF ENDODONTICS, 2014, 40 (04) :S41-S45