2022, Number 1
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Sal Jal 2022; 9 (1)
Celulas troncales aisladas de piezas dentales provenientes de población mexicana el Estado de Jalisco
Sánchez-Gómez I, Gonzáles-Pelayo GL, Santibáñez-Escobar LP, Gaona-Bernal J, Villa-García Torres LS, Márquez-García E, Avelar-Rodríguez FJ, Marino-Marmolejo EN, Flores-Hernández FY
Language: Spanish
References: 35
Page: 16-27
PDF size: 482.39 Kb.
ABSTRACT
Research on stem cells regenerating damaged tissues has
grown due to the potential to improve various ailments.
Tooth stem cells are an option to be used in tissue
engineering, requiring standardized procedures for their
processing in order to achieve adequate isolation and
culture.
Objective: To carry out an evaluation of different
procedures for the isolation, culture and propagation of
dental pulp stem cells (DPSC).
Materials and Methods:
Quasi-experimental study with non-probabilistic
sampling for isolation of DPSC, donated under informed
consent. Various methods were tried; for access to the pulp
chamber, mechanical drilling was tested using milling
machines and high-speed handpieces, as well as a cutting
method at the cervical third level dividing crown and
root using a low-speed handpiece with a diamond disc.
The dental pulp was extracted by disintegrating the cells
by various enzymatic methods proceeding to monolayer
culture for isolation. Cell phenotyping was by flow
cytometry detecting mesenchymal markers (CD44, 73, 90,
105); in addition, multidifferentiation tests were carried
out towards osteogenic, chondrogenic and adipogenic
lineages. Finally, the DPSCs were cryopreserved in liquid
nitrogen.
Results: Efficient procedure for obtaining,
isolating and proliferating DPSC, confirming with
morphology, expression of mesenchymal markers,
multipotentiality and plastic adhesion.
Conclusion: A
DPSC isolation protocol was standardized (transport,
dental processing, isolation, culture and proliferation),
observing better isolation of DPSC from molars with
immature apex, from patients with an average age of 25
years.
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