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This article provides a stepwise guide to establish a primary culture of dental pulps stem cells using the explant culture method and characterization of these cells based on ICSCRT guidelines. The cells isolated by this protocol can be considered as mesenchymal stem cells for further applications.
The human dental pulp represents a promising multipotent stem cell reservoir with pre-eminent regenerative competence that can be harvested from an extracted tooth. The neural crest-derived ecto-mesenchymal origin of dental pulp stem cells (DPSCs) bestows a high degree of plasticity that owes to its multifaceted benefits in tissue repair and regeneration. There are various practical ways of harvesting, maintaining, and proliferating adult stem cells being investigated for their use in regenerative medicine. In this work, we demonstrate the establishment of a primary mesenchymal stem cell culture from dental tissue by the explant culture method. The isolated cells were spindle-shaped and adhered to the plastic surface of the culture plate. The phenotypic characterization of these stem cells showed positive expression of the international society of cell therapy (ISCT)-recommended cell surface markers for MSC, such as CD90, CD73, and CD105. Further, negligible expression of hematopoietic (CD45) and endothelial markers (CD34), and less than 2% expression of HLA-DR markers, confirmed the homogeneity and purity of the DPSC cultures. We further illustrated their multipotency based on differentiation to adipogenic, osteogenic, and chondrogenic lineages. We also induced these cells to differentiate into hepatic-like and neuronal-like cells by adding corresponding stimulation media. This optimized protocol will aid in the cultivation of a highly expandable population of mesenchymal stem cells to be utilized in the laboratory or for preclinical studies. Similar protocols can be incorporated into clinical setups for practicing DPSC-based treatments.
Adult stem cells have transpired into a powerful therapeutic tool for cell-directed treatments and therapies due to their plasticity, paracrine mechanisms, and immunomodulatory properties1,2,3. The encouraging data from stem cell-based preclinical studies have inspired researchers to work for the bench to-bedside translation. The type of stem cells used for stem cell therapy plays a significant role in successful outcomes. In preclinical and clinical studies, the most widely reported source for mesenchymal stem cells (MSCs) remain bone marrow4,
All the procedures described in the study have been approved by the Institute Ethics Committee (IEC# 9195/PG-12 ITRG/2571-72) of PGIMER, Chandigarh. All the cell culture related experiments need to be performed in a Class II biological safety cabinet (BSC) following aseptic technique. Dental pulp was obtained from healthy teeth of three (F/14, M/14, and M/20) patients undergoing third molar extractions for orthodontic reasons. Before the sample collection, written informed consent was obtained from the patient/guardian i.......
Here, we describe how researchers can establish a pure culture of DPSCs via the explant method6,7,8,9,10 and induce them toward multiple lineages to establish the purity of culture for downstream applications.
We established a primary culture of DPSCs from the small tissue of pulp extracted from the third molar tooth of pat.......
Stem cells have pinned the hopes of curing numerous diseases, owing to their plasticity, robustness, immunomodulatory properties, paracrine mechanisms, and homing efficiencies. Dental pulp tissue is considered the most potent and valuable source of stem cells, with eminent plasticity and a regenerative capability. Here, we demonstrate the isolation of DPSCs, utilizing the widely adopted explant culture method, in which the cells migrate from pieces of pulp tissue or explants to grow into a homogenous cell culture that mo.......
We acknowledge the funding support to AK from the Department of Health Research (DHR), ICMR, Govt. of India (DHR-NRI Grant # R.12015/01/2022-HR). SR has received funding from ICMR, Govt. of India (Grant # 2020-7593/SCR-BMS) and PS has received fellowship from CSIR, Govt. of India. We are also thankful to Ms. Sandhya Tokhi and Ms. Bhupinder Kaur for assistance in flow cytometry, and central sophisticated instrumentation core (CSIC) and PGIMER, Chandigarh for providing infrastructural support.
....Name | Company | Catalog Number | Comments |
6 well cell culture plate | Costar | 3516 | For cell culture |
Alcian blue stain | EZstain chondrocyte staining kit, HiMedia | CCK029 | |
alizarin red S stain | Sigma-Aldrich | TMS-008 | Osteogenic stain |
Antibiotic cocktail | Himedia | A002-5X50ML | To prevent culture contamination |
Ascorbic Acid | Himedia | TC094-25G | Chondrogenic induction |
B27 supplement | Gibco | 17504044 | For neural induction |
bFGF ( basic Fibroblast Growth Factor) | Gibco | PHG0024 | For neural induction |
CD 105 | BD-Pharmingen | 560839 | |
CD 35 | Biolegend | 343604 | |
CD 45 | Biolegend | 304006 | |
CD 73 | Biolegend | 344016 | |
CD 90 | Biolegend | 328107 | Characterization |
cetyl pyridinium chloride (CPC) | Sigma-Aldrich | 1104006 | For Alizarin Red extraction |
Dexamethasone 21-phosphate disodium | Sigma-Aldrich | D1159-100MG | |
Dulbecco's Phosphate Buffered Saline | Himedia | TS1006-5L | For washing purpose |
EGF (Epidermal Growth Factor) | Gibco | PHG0311 | For hepatic and neural induction |
EVOS LED microscope | Invitrogen | For fluorescence imaging | |
EZ stain Chondrocyte staining kit | Himedia | CCK029-1KT | Chondro stain Kit |
FACS Canto flow cytometer | BD Biosciences | For cell characterization | |
Fetal Bovine Serum | Gibco | 16000044 | For primary culture |
Fetal Bovine Serum | Sigma-Aldrich | F2442 | For cell culture |
G5 supplement | Gibco | 17503012 | For neural induction |
HGF( Hepatocyte Growth Factor) | Sigma-Aldrich | H1404 | For hepatic Induction |
HLA-DR | Biolegend | 307605 | |
 Human TGF-β3 | Peprotech | #100-36E-10U | |
Insulin-Transferrin-Selenous acid premix | Sigma-Aldrich | I3146 | For hepatic Induction |
ITS premix | Corning | 354350 | |
LDL Uptake Assay kit | Abcam | ab133127 | For hepatic characterization |
Low glucose DMEM | Gibco | 11885-084 | For hepatic induction |
MAP2 antibody | Sigma-Aldrich | M4403 | For neural characterization |
N2 supplement | Gibco | 17502048 | For neural induction |
Neural Basal Media | Gibco | 21103049 | For neural induction |
NFM antibody | Sigma-Aldrich | N4142 | For neural characterization |
Nikon Elipse TS100 microscope | Nikon | For fluorescence imaging | |
Oil Red O | Sigma-Aldrich | 01391-250Ml | Adipogenic stain |
Oncostatin M | R&D Systems | 295-OM-010/CF | For hepatic Induction |
Petridish | Tarson | 460090-90MM | For tissue cutting |
Potassium phosphate monobasic | Sigma-Aldrich | 15655-100G | Osteogenic induction |
Propan-2-ol | Thermo Fisher | Q13827 | For Oil Red O extraction |
Sodium pyruvate solution | Sigma life sciences | S8636-100ML | |
Trypsin-EDTA | Sigma-Aldrich | T4049 | For cell passaging |
Whatman filter paper | merck | WHA1001325 | filter paper |
α- Minimum Essential Media (α-MEM) | Sigma-Aldrich | M0643-10X 1L | Media for primary culture |
β-glycerophosphate disodium salt hydrate | Sigma-Aldrich | G9422-50G |
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