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Isolation and culture of dental pulp stem cells from permanent and deciduous teeth.
Naz, Shagufta; Khan, Farhan Raza; Zohra, Raheela Rahmat; Lakhundi, Sahreena Salim; Khan, Mehwish Sagheer; Mohammed, Nuruddin; Ahmad, Tashfeen.
Afiliación
  • Naz S; Ms. Shagufta Naz, M.Sc., Department of Surgery, Department of Biotechnology, University of Karachi, Pakistan. Aga Khan University, Karachi, Pakistan.
  • Khan FR; Dr. Farhan Raza Khan, FCPS, Department of Surgery, Aga Khan University, Karachi, Pakistan.
  • Zohra RR; Dr. Raheela Rahmat Zohra, Ph.D. Department of Biotechnology, University of Karachi, Pakistan.
  • Lakhundi SS; Dr. Sahreena Lakhundi, Ph.D., Department of Surgery, Aga Khan University, Karachi, Pakistan.
  • Khan MS; Ms. Mehwish Sagheer Khan, M.Sc. M.Phil., Department of Surgery, Aga Khan University, Karachi, Pakistan.
  • Mohammed N; Dr. Nuruddin Mohammed, PhD, FMFM, Department of Obstetrics and Gynecology, Aga Khan University, Karachi, Pakistan.
  • Ahmad T; Dr. Tashfeen Ahmad, FCPS, Ph.D., Departments of Surgery and Biological & Biomedical Sciences, Aga Khan University, Karachi, Pakistan.
Pak J Med Sci ; 35(4): 997-1002, 2019.
Article en En | MEDLINE | ID: mdl-31372131
ABSTRACT

OBJECTIVE:

To isolate dental pulp mesenchymal stem cells (MSCs) from non-infected human permanent and deciduous teeth.

METHODS:

It was an in-vitro experimental study. Human teeth were collected from 13 apparently healthy subjects including nine adults and four children. After decoronation dental pulps were extirpated from teeth and cultured via explant method in a stem cell defined media. Data was analyzed by descriptive statistics.

RESULTS:

As above MSCs emerged exhibiting fibroblast-like morphology. In vitro culture was positive for 100% (9/9) and 75% (3/4) of the permanent and deciduous teeth respectively. First cell appeared from deciduous teeth pulp in 10±6.2 days while permanent teeth pulp took 12.4±3.7 days. Together, 26.6±3.6 and 24.5±3.5 days were required for permanent and deciduous tooth pulp stem cells to be ready for further assays.

CONCLUSIONS:

The protocol we developed is easy and consistent and can be used to generate reliable source of MScs for engineering of calcified and non-calcified tissue for regenerative medicine approaches.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pak J Med Sci Año: 2019 Tipo del documento: Article País de afiliación: Pakistán

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Pak J Med Sci Año: 2019 Tipo del documento: Article País de afiliación: Pakistán
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