Isolation, Culture, and Characterization of Dental Pulp Stem Cells from Human Deciduous and Permanent Teeth

被引:3
作者
Anil, Sukumaran [1 ,2 ]
Thomas, Nebu G. [2 ]
Chalisserry, Elna P. [2 ]
Dalvi, Yogesh B. [2 ]
Ramadoss, Ramya [3 ]
Vellappally, Sajith [4 ]
机构
[1] Hamad Med Corp, Oral Hlth Inst, Dept Dent, Doha, Qatar
[2] Pushpagiri Inst Med Sci & Res Ctr, Tiruvalla, India
[3] Saveetha Inst Med & Tech Sci, Saveetha Dent Coll, Chennai, India
[4] King Saud Univ, Coll Appl Med Sci, Riyadh, Saudi Arabia
来源
JOVE-JOURNAL OF VISUALIZED EXPERIMENTS | 2024年 / 207期
关键词
DIFFERENTIATION; TISSUES; CRYOPRESERVATION; BANKING;
D O I
10.3791/65767
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页数:18
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