A method is shown here for the preparation of the tongue extracellular matrix (TEM) with efficient decellularization. The TEM can be used as functional scaffolds for the reconstruction of a tongue squamous cell carcinoma (TSCC) model under static or stirred culture conditions.
In order to construct an effective and realistic model for tongue squamous cell carcinoma (TSCC) in vitro, the methods were created to produce decellularized tongue extracellular matrix (TEM) which provides functional scaffolds for TSCC construction. TEM provides an in vitro niche for cell growth, differentiation, and cell migration. The microstructures of native extracellular matrix (ECM) and biochemical compositions retained in the decellularized matrix provide tissue-specific niches for anchoring cells. The fabrication of TEM can be realized by deoxyribonuclease (DNase) digestion accompanied with a serious of organic or inorganic pretreatment. This protocol is easy to operate and ensures high efficiency for the decellularization. The TEM showed favorable cytocompatibility for TSCC cells under static or stirred culture conditions, which enables the construction of the TSCC model. A self-made bioreactor was also used for the persistent stirred condition for cell culture. Reconstructed TSCC using TEM showed the characteristics and properties resembling clinical TSCC histopathology, suggesting the potential in TSCC research.
The tongue has various important functions, such as deglutition, articulation, and tasting. Thus, the impairment of tongue function has great impact on patients' quality of life1. The most common malignancy in the oral cavity is tongue squamous cell carcinoma (TSCC), which usually occurs in people who drink alcohol or smoke tobacco2.
In recent years, little progress has been achieved in fundamental research on TSCC. The lack of efficient in vitro research models remains to be one of the biggest problems. Thus, the extracellular matrix (ECM) turns out to be a potential solution. Since ECM is a complex network frame composed of highly organized matrix components, scaffold materials having an ECM-like structure and composition would be competent for cancer research. Decellularized ECM can perfectly provide the niche for the cells from the same origin in vitro, which turns out to be the most significant advantage of ECM.
ECM can be retained with cellular components being removed from the tissues through the decellularization using detergents and enzymes. Various ECM components, including collagen, fibronectin, and laminin in decellularized matrix provide a native-tissue-like microenvironment for cultured cells, promoting the survival, proliferation, and differentiation of the cells3. Moreover, the immunogenicity for transplantation can be reduced to a minimal level with the absence of cellular components in ECM.
So far, fabrication methods for decellularized ECM have been tried in different tissues and organs, such as heart4,5,6,7, liver8,9,10,11, lung12,13,14,15,16,17, and kidney18,19,20. However, no relevant research has be found on similar work in the tongue to the best of our knowledge.
In this study, decellularized tongue extracellular matrix (TEM) was fabricated both efficiently and cheaply by a series of physical, chemical, and enzymatic treatment. Then the TEM was used to recapitulate TSCC in vitro, showing an appropriate simulation for TSCC behavior and development. TEM has good biocompatibility as well as the ability to guide the cells to the tissue-specific niche, which indicates that TEM may have great potential in TSCC research3. The protocol shown here provides a choice for researchers studying on either pathogenesis or clinical therapies of TSCC.
All animal work was performed in accordance with animal welfare act, institutional guidelines and approved by Institutional Animal Care and Use Committee, Sun Yat-sen University.
1. Preparation of TEM
2. Three-dimensional (3D) Reconstitution of TSCC
This protocol for the preparation of TEM turns out to be efficient and appropriate. The TEM showed perfect decellularization compared with native tongue tissues. The efficacy of decellularization was confirmed by hematoxylin-eosin (HE) staining (Figure 1A-B). The HE staining results revealed complete disappearance of nuclear staining in TEM (Figure 1B). Moreover, DNA content quantification from previous work showed that DNA was almost completely removed from TEM3. This protocol also showed rare damage to the tissue integrity while removing cell components (Figure 1B).
3D reconstitution of TSCC using TEM and a self-made minibioreactor (Figure 2A-B) achieved satisfying results. HE staining showed that Cal27 cells in the TEM presented typical TSCC pathological characteristics (Figure 2C-D). The cells in stirred culture conditions presented single-cell migration (Figure 2C) or collective migration (Figure 2D) in different lesion areas. In static culture conditions, Cal27 cells also formed invasive structures in the TEM, but it took a longer time (Figure 2E). Furthermore, a human osteosarcoma cell line U2OS was also introduced to the same stirred culture system. Though U2OS cells could live in the culture medium, they were not found in the TEM (Figure 2F). The TEM showed different biocompatibility for different types of cancer cells, suggesting that different tumor cells may need different microenvironments to flourish.
Figure 1: Preparation of TEM. (A) HE staining of native tongues from mice. Scale bar = 100 µm. (B) HE staining of decellularized TEM from mice. Scale bar = 100 µm. Please click here to view a larger version of this figure.
Figure 2: Reconstitution of TSCC by TEM. (A) The overview of a self-made minibioreactor. (B) The view of the TEM-loading position of a self-made minibioreactor. (C) HE staining of 14-day stirred cultured TSCC with TEM. Single cell invasion phenomena are indicated by black arrows. Scale bar = 50 µm. (D) HE staining of 14-day stirred cultured TSCC with TEM. Collective invasion phenomena are indicated by black arrows. Scale bar = 50 µm. (E) HE staining of 28-day static cultured TSCC with TEM. Single cell invasion phenomena are indicated by black arrows. Scale bar = 100 µm. (F) HE staining of 14-day stirred cultured U2OS cells with TEM. Scale bar = 50 µm. Please click here to view a larger version of this figure.
A well-established protocol for decellularized ECM fabrication should retain the native ECM composition while removing cellular components in tissues nearly completely21. Despite currently reported decellularization protocols which require perfusion through the vasculature to remove cellular materials by convective transport, mechanical agitation was adopted here, known as a traditional simple and cheap method22,23,24,25,26. Moreover, since the tongue is rich in lingualis and has few bulky vascular vessels, this protocol is more suitable for tongue tissues than other protocols described above.
Furthermore, this protocol for TEM production carries out an appropriate moderate-strength decellularization, avoiding the destruction or dissolution of the base membrane which may be caused by high-strength decellularization such as sodium dodecyl sulfate (SDS) treatment3. In addition, the protocol also worked effectively in the tongue of rat and pig (data not shown), suggesting that the method could be commonly used upon tongues from various species3.
It's worth noting that there are some critical steps or details in this protocol, which could directly influence the results. One important step is the digestion of tongue cells by DNase. If the digestion time is not enough or the DNase doesn't work efficiently, the decellularization of the tongue would hardly be achieved. Another thing which should be noticed is that the rotary speed for the bioreactor shouldn't be too fast, considering the damage to TEM. Moreover, a sterile environment for this operation is very important in the protocol.
In spite of the strict rules above, the protocol for TEM preparation can be adjusted to some extent. Washing the tongues with ultrapure water or PBS for a few more hours than the time which the protocol suggests would not obviously affect the fabrication of TEM. However, since the protocol needs almost one week to prepare the TEM, it cannot meet immediate demands for TEM.
The TEM shows great value in TSCC model construction. Together with a self-made minibioreactor, suspended Cal27 cells can attach in TEM and form similar infiltrative structure resembling human TSCC histopathology3. This could be an ideal model for monitoring and investigating the invasion and metastasis of TSCC in vitro. The model could also benefit the work on drug tests on TSCC. In consideration of all these, the protocol presented here may have great potential in TSCC research.
The authors have nothing to disclose.
The authors acknowledge the support of research grants from National Natural Science Foundation of China (31371390), the Program of the State High-Tech Development Project (2014AA020702) and the program of Guangdong Science and Technology (2016B030231001).
C57-BL/6J mice | Sun Yat-sen University Laboratory Animal Center | ||
Ethanol | Guangzhou Chemical Reagent Factory | HB15-GR-2.5L | |
Sodium chloride | Sangon Biotech | A501218 | |
Potassium chloride | Sangon Biotech | A100395 | |
Dibasic Sodium Phosphate | Guangzhou Chemical Reagent Factory | BE14-GR-500G | |
Potassium Phosphate Monobasic | Sangon Biotech | A501211 | |
1.5 mL EP tube | Axygen | MCT-150-A | |
Ultra-low temperature freezer | Thermo Fisher Scientific | ||
3.5 cm cell culture dish | Thermo Fisher Scientific | 153066 | |
6 cm cell culture dish | Greiner | 628160 | |
Triton X-100 | Sigma-Aldrich | V900502 | |
Calcium chloride | Sigma-Aldrich | 746495 | |
Magnesium chloride | Sigma-Aldrich | 449164 | |
DNase | Sigma-Aldrich | D5025 | |
Magnesium sulphate | Sangon Biotech | A601988 | |
Glucose | Sigma-Aldrich | 158968 | |
Sodium bicarbonate | Sigma-Aldrich | S5761 | |
Ampicillin | Sigma-Aldrich | A9393 | |
Kanamycin | Sigma-Aldrich | PHR1487 | |
Surgical suture | Shanghai Jinhuan | ||
250 mL wide-mouth bottle | SHUNIU | 1407 | |
Magnetic stirrer | AS ONE | 1-4602-32 | |
CO2 incubator | SHEL LAB | SCO5A | |
10 mL syringe | Hunan Pingan | ||
50 mL centrifuge tube | Greiner | 227270 | |
Cal27 cell | Chinese Academy of Science, Shanghai Cell Bank | Tongue squamous cell carcinoma cell line | |
U2OS cell | Chinese Academy of Science, Shanghai Cell Bank | Human osteosarcoma cell line | |
DMEM/F12 | Sigma-Aldrich | D0547 | |
Sodium pyruvate | Sigma-Aldrich | P5280 | |
Hepes free acid | BBI | A600264 | |
FBS | Hyclone | SH30084.03 | |
4 °C fridge | Haier | ||
Water purifier | ELGA | ||
Hemocytometer | BLAU | 717805 |