Journal of Endodontics
Volume 36, Issue 2 , Pages 238-243, February 2010

Effect of Wnt6 on Human Dental Papilla Cells In Vitro

  • Chenglin Wang, MS, DDS

      Affiliations

    • West China School of Stomatology, Sichuan University, Sichuan, China
    • State Key Laboratory of Oral Diseases, Sichuan University, Sichuan, China
  • ,
  • Libin Ren, DDS

      Affiliations

    • West China School of Stomatology, Sichuan University, Sichuan, China
  • ,
  • Li Peng, MS, DDS

      Affiliations

    • West China School of Stomatology, Sichuan University, Sichuan, China
    • State Key Laboratory of Oral Diseases, Sichuan University, Sichuan, China
  • ,
  • Ping Xu, MS, DDS

      Affiliations

    • West China School of Stomatology, Sichuan University, Sichuan, China
    • State Key Laboratory of Oral Diseases, Sichuan University, Sichuan, China
  • ,
  • Gang Dong, DDS

      Affiliations

    • West China School of Stomatology, Sichuan University, Sichuan, China
  • ,
  • Ling Ye, PhD, DDS

      Affiliations

    • West China School of Stomatology, Sichuan University, Sichuan, China
    • State Key Laboratory of Oral Diseases, Sichuan University, Sichuan, China
    • Corresponding Author InformationAddress requests for reprints to Ling Ye, 14#, 3rd section of Ren Ming Nan Lu, West China School of Stomatology, Sichuan University, Chengdu, Sichuan, China 610041.

published online 26 October 2009.

Abstract 

Introduction

The Wnt signaling pathway plays an important role in tissue development by acting on proliferation, differentiation, and cell fate decisions. Because the role of Wnt6 in tooth development was still unknown, the purpose of this study was to investigate the role of Wnt6 in tooth morphogenesis and dental tissue mineralization by elucidating its effect on human dental papilla cells (hDPCs) in vitro.

Methods

Human dental papilla cells were enzymatically separated from tooth germs. Recombinant adenovirus encoding full-length Wnt6 cDNA was constructed to overexpress Wnt6, and the biologic effects of Wnt6 on hDPCs were investigated. Wnt6-transduced changes in hDPC proliferation were examined by means of a 5-bromodeoxyuridine (BrdU) incorporation assay and cell cycle analysis. Wnt6-transduced changes in hDPC differentiation were investigated by evaluating alkaline phosphatase (ALPase) activity, by a mineralization assay, and analysis of mineralization-related gene expression including ALP, type I collagen (Col I), osteonectin (ON), osteopontin (OPN), bone sialoprotein (BSP), and dentin matrix protein-1 (DMP-1).

Results

Wnt6 overexpression had no significant effect on the proliferation of hDPCs by BrdU incorporation assay and flow cytometric analysis. Wnt6 enhanced differentiation of hDPCs into functional odontoblast-like cells with up-regulated activity of ALPase and the expression of mineralization-related genes such as ALP, Col I, ON, OPN, BSP, and DMP-1. Wnt6 overexpression also promoted the mineralization of hDPCs.

Conclusions

Our findings verified that Wnt6 plays an important role in tooth development by promoting hDPC differentiation, without significant effects on hDPC proliferation.

Key Words: Differentiation, human dental papilla cells, proliferation, Wnt6

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 20.00 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0099-2399(09)00767-5

doi:10.1016/j.joen.2009.09.007

Journal of Endodontics
Volume 36, Issue 2 , Pages 238-243, February 2010