CC BY-NC-ND 4.0 · Eur J Dent 2020; 14(01): 123-127
DOI: 10.1055/s-0040-1702900
Original Article

Concanavalin A Enhanced Proliferation and Osteogenic Differentiation of Dental Pulp Stem Cells

Ketut Suardita
1   Department of Conservative Dentistry, Faculty of Dental Medicine, Universitas Airlangga, Jawa Timur, Indonesia
,
Ira Arundina
2   Department of Oral Biology, Faculty of Dental Medicine, Universitas Airlangga, Jawa Timur, Indonesia
,
Udijanto Tedjosasongko
3   Department of Pediatric Dentistry, Faculty of Dental Medicine, Universitas Airlangga, Jawa Timur, Indonesia
,
Anita Yuliati
4   Department of Dental Material, Faculty of Dental Medicine, Universitas Airlangga, Jawa Timur, Indonesia
,
Harry Huiz Peeters
5   Laser Research Center in Dentistry, Bandung, Indonesia
,
I Komang Evan Wijaksana
6   Department of Periodontics, Faculty of Dental Medicine, Universitas Airlangga, Jawa Timur, Indonesia
,
7   Department of Oral Medicine, Faculty of Dental Medicine, Universitas Airlangga, Indonesia
› Author Affiliations

Abstract

Objective Dental pulp stem cells (DPSCs) can be used as a component in the formation of regenerative dentine during direct pulp capping therapy. Concanavalin A (ConA) is a type of lectin with a molecular weight of 26 kDa derived from the Canavalia ensiformis plant. Lectins possess strong proliferation and differentiation abilities in various animal cells including lymphocytes, osteoblasts, and chondrocytes. The aim of study was to determine the effect of ConA on the proliferation and osteogenic differentiation of DPSCs in vitro.

Materials and Methods In this in vitro study, DPSCs were isolated from third molars before ConA induction was performed at concentrations of 5 and 10 μg/mL. The proliferation assay was determined by 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay. Osteogenic differentiation was determined by means of mineralization.

Statistical Analysis Data were analyzed using analysis of variance and a Student’s t-test. The p-value was set at 0.05.

Results The addition of 5 and 10 µg/mL of ConA to DPSCs can significantly increase the proliferation and osteogenic differentiation of DPSCs (p ≤0.05).

Conclusion ConA can increase the proliferation and osteogenic differentiation of DPSCs.



Publication History

Article published online:
13 March 2020

© .

Thieme Medical and Scientific Publishers Private Ltd.
A-12, Second Floor, Sector -2, NOIDA -201301, India

 
  • References

  • 1 Ponnaiyan D, Jegadeesan V. Comparison of phenotype and differentiation marker gene expression profiles in human dental pulp and bone marrow mesenchymal stem cells. Eur J Dent 2014; 8 (03) 307-313
  • 2 Gronthos S, Mankani M, Brahim J, Robey PG, Shi S. Postnatal human dental pulp stem cells (DPSCs) in vitro and in vivo. Proc Natl Acad Sci U S A 2000; 97 (25) 13625-13630
  • 3 Arthur A, Rychkov G, Shi S, Koblar SA, Gronthos S. Adult human dental pulp stem cells differentiate toward functionally active neurons under appropriate environmental cues. Stem Cells 2008; 26 (07) 1787-1795
  • 4 Sugiyama M, Iohara K, Wakita H. et al. Dental pulp-derived CD31-/CD146- side population stem/progenitor cells enhance recovery of focal cerebral ischemia in rats. Tissue Eng Part A 2011; 17 (9-10): 1303-1311
  • 5 Miura M, Gronthos S, Zhao M. et al. SHED: stem cells from human exfoliated deciduous teeth. Proc Natl Acad Sci USA 2003; 100 (10) 5807-5812
  • 6 Laino G, Graziano A, d’Aquino R. et al. An approachable human adult stem cell source for hard-tissue engineering. J Cell Physiol 2006; 206 (03) 693-701
  • 7 d’Aquino R, Graziano A, Sampaolesi M. et al. Human postnatal dental pulp cells co-differentiate into osteoblasts and endotheliocytes: a pivotal synergy leading to adult bone tissue formation. Cell Death Differ 2007; 14 (06) 1162-1171
  • 8 Simpson AH, Mills L, Noble B. The role of growth factors and related agents in accelerating fracture healing. J Bone Joint Surg Br 2006; 88 (06) 701-705
  • 9 Hanada K, Dennis JE, Caplan AI. Stimulatory effects of basic fibroblast growth factor and bone morphogenetic protein-2 on osteogenic differentiation of rat bone marrow-derived mesenchymal stem cells. J Bone Miner Res 1997; 12 (10) 1606-1614
  • 10 Yan W, Pan H, Ishida H. et al. Effects of concanavalin A on chondrocyte hypertrophy and matrix calcification. J Biol Chem 1997; 272 (12) 7833-7840
  • 11 Oda R, Suardita K, Fujimoto K. et al. Anti-membrane-bound transferrin-like protein antibodies induce cell-shape change and chondrocyte differentiation in the presence or absence of concanavalin A. J Cell Sci 2003; 116 (Pt 10): 2029-2038
  • 12 Sekiya K, Nishimura M, Suehiro F, Nishimura H, Hamada T, Kato Y. Enhancement of osteogenesis by concanavalin A in human bone marrow mesenchymal stem cell cultures. Int J Artif Organs 2008; 31 (08) 708-715
  • 13 Hilkens P, Gervois P, Fanton Y. et al. Effect of isolation methodology on stem cell properties and multilineage differentiation potential of human dental pulp stem cells. Cell Tissue Res 2013; 353 (01) 65-78
  • 14 Dominici M, Le Blanc K, Mueller I. et al. Minimal criteria for defining multipotent mesenchymal stromal cells. The International Society for Cellular Therapy position statement. Cytotherapy 2006; 8 (04) 315-317
  • 15 Byun YK, Kim KH, Kim SH. et al. Effects of immunosuppressants, FK506 and cyclosporin A, on the osteogenic differentiation of rat mesenchymal stem cells. J Periodontal Implant Sci 2012; 42 (03) 73-80
  • 16 Bakopoulou A, Apatzidou D, Aggelidou E. et al. Isolation and prolonged expansion of oral mesenchymal stem cells under clinical-grade, GMP-compliant conditions differentially affects “stemness” properties. Stem Cell Res Ther 2017; 8 (01) 247
  • 17 Yang H, Li J, Sun J. et al. Cells isolated from cryopreserved dental follicle display similar characteristics to cryopreserved dental follicle cells. Cryobiology 2017; 78: 47-55
  • 18 Rodas-Junco BA, Villicaña C. Dental pulp stem cells: current advances in isolation, expansion and preservation. Tissue Eng Regen Med 2017; 14 (04) 333-347
  • 19 Batouli S, Miura M, Brahim J. et al. Comparison of stem-cell-mediated osteogenesis and dentinogenesis. J Dent Res 2003; 82 (12) 976-981
  • 20 Yan WQ, Nakashima K, Iwamoto M, Kato Y. Stimulation by concanavalin A of cartilage-matrix proteoglycan synthesis in chondrocyte cultures. J Biol Chem 1990; 265 (17) 10125-10131
  • 21 Nakamasu K, Kawamoto T, Shen M. et al. Membrane-bound transferrin-like protein (MTf): structure, evolution and selective expression during chondrogenic differentiation of mouse embryonic cells. Biochim Biophys Acta 1999; 1447 (2-3): 258-264
  • 22 De Mejía EG, Prisecaru VI. Lectins as bioactive plant proteins: a potential in cancer treatment. Crit Rev Food Sci Nutr 2005; 45 (06) 425-445
  • 23 Liu B, Li CY, Bian HJ, Min MW, Chen LF, Bao JK. Antiproliferative activity and apoptosis-inducing mechanism of Concanavalin A on human melanoma A375 cells. Arch Biochem Biophys 2009; 482 (1-2) 1-6
  • 24 Chen D, Zhao M, Mundy GR. Bone morphogenetic proteins. Growth Factors 2004; 22 (04) 233-241