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Isolation, Culture, and Characterization of Dental Pulp Stem Cells from Human Deciduous and Permanent Teeth.
Anil, Sukumaran; Thomas, Nebu G; Chalisserry, Elna P; Dalvi, Yogesh B; Ramadoss, Ramya; Vellappally, Sajith.
Afiliación
  • Anil S; Department of Dentistry, Oral Health Institute, Hamad Medical Corporation; Pushpagiri Institute of Medical Sciences and Research Centre; drsanil@gmail.com.
  • Thomas NG; Pushpagiri Institute of Medical Sciences and Research Centre.
  • Chalisserry EP; Pushpagiri Institute of Medical Sciences and Research Centre.
  • Dalvi YB; Pushpagiri Institute of Medical Sciences and Research Centre.
  • Ramadoss R; Saveetha Dental College, Saveetha Institute of Medical and Technical Sciences.
  • Vellappally S; College of Applied Medical Sciences, King Saud University.
J Vis Exp ; (207)2024 May 17.
Article en En | MEDLINE | ID: mdl-38829121
ABSTRACT
In the realm of regenerative medicine and therapeutic applications, stem cell research is rapidly gaining traction. Dental pulp stem cells (DPSCs), which are present in both deciduous and permanent teeth, have emerged as a vital stem cell source due to their accessibility, adaptability, and innate differentiation capabilities. DPSCs offer a readily available and abundant reservoir of mesenchymal stem cells, showcasing impressive versatility and potential, particularly for regenerative purposes. Despite their promise, the main hurdle lies in effectively isolating and characterizing DPSCs, given their representation as a minute fraction within dental pulp cells. Equally crucial is the proper preservation of this invaluable cellular resource. The two predominant methods for DPSC isolation are enzymatic digestion (ED) and outgrowth from tissue explants (OG), often referred to as spontaneous growth. This protocol concentrates primarily on the enzymatic digestion approach for DPSC isolation, intricately detailing the steps encompassing extraction, in-lab processing, and cell preservation. Beyond extraction and preservation, the protocol delves into the differentiation prowess of DPSCs. Specifically, it outlines the procedures employed to induce these stem cells to differentiate into adipocytes, osteoblasts, and chondrocytes, showcasing their multipotent attributes. Subsequent utilization of colorimetric staining techniques facilitates accurate visualization and confirmation of successful differentiation, thereby validating the caliber and functionality of the isolated DPSCs. This comprehensive protocol functions as a blueprint encompassing the entire spectrum of dental pulp stem cell extraction, cultivation, preservation, and characterization. It underscores the substantial potential harbored by DPSCs, propelling forward stem cell exploration and holding promise for future regenerative and therapeutic breakthroughs.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre / Diente Primario / Pulpa Dental Límite: Humans Idioma: En Revista: J Vis Exp Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Células Madre / Diente Primario / Pulpa Dental Límite: Humans Idioma: En Revista: J Vis Exp Año: 2024 Tipo del documento: Article Pais de publicación: Estados Unidos