Isolation and Expansion of Human Glioblastoma Multiforme Tumor Cells Using the Neurosphere Assay

Summary

This video protocol demonstrates the isolation and expansion of stem like cells from surgically resected human glioblastoma mutliforme (GBM) tumor tissue using the neurosphere assay culture method.

Abstract

Stem-like cells have been isolated in tumors such as breast, lung, colon, prostate and brain. A critical issue in all these tumors, especially in glioblastoma mutliforme (GBM), is to identify and isolate tumor initiating cell population(s) to investigate their role in tumor formation, progression, and recurrence. Understanding tumor initiating cell populations will provide clues to finding effective therapeutic approaches for these tumors. The neurosphere assay (NSA) due to its simplicity and reproducibility has been used as the method of choice for isolation and propagation of many of this tumor cells. This protocol demonstrates the neurosphere culture method to isolate and expand stem-like cells in surgically resected human GBM tumor tissue. The procedures include an initial chemical digestion and mechanical dissociation of tumor tissue, and subsequently plating the resulting single cell suspension in NSA culture. After 7-10 days, primary neurospheres of 150-200 μm in diameter can be observed and are ready for further passaging and expansion.

Protocol

1. Collection of Primary GBM Tissue

1. A glioblastoma mutliforme (GBM) tumor is obtained from a patient diagnosed with the cancer and undergoing surgery.
2. Arrangements must be made with neurosurgery team. The neurosurgeon will place the resected GBM tumor in an appropriate size tube containing neural stem cell (NSC) basal medium supplemented with 10-15% antibiotics (Peniciline/Streptomycine). Cold medium must be provided to operating room by lab. Alternatively, cold HEPES-buffered minimum essential medium (HEM) or phosphate buffered saline (PBS) with high concentration of antibiotics can also be used for this purpose.
3. The resected tumor tissue is delivered to the lab on ice and placed under the hood.

2. Dissociation of Primary Tumor into Single-Cell Suspension

1. Excess of the original medium/PBS is removed from the falcon tube and the sample is washed 2-3 times with 5-10ml of PBS/NSC basal medium to remove blood and debris. The PBS/Medium is removed and the GBM tumor tissue is placed in a Petri dish.
2. The tissue is cut into small pieces and minced with a No. 10 scalpel blade into tiny pieces to increase the surface area for trypsinization process. Mincing can take 1-3 minutes depending on the size of the tumor.
3. The minced tissue is trypsinized in 3-5ml of pre-warmed %0.05 trypsin-EDTA for 10-15 minutes at a 37°C water bath. An electronic pipette is used to transfer the tiny tumor pieces and trypsin into a 15ml Falcon tube.
4. An equal volume of soybean trypsin inhibitor is added to stop the enzymatic trypsin reaction after the incubation period.
5. Trypsin inactivation is ensured by pipetting the suspension up and down several times. Then, the suspension is pelleted down by centrifuging at 800rpm (110g) for 5min.
6. The supernatant is discarded and the tissue pieces are resuspended in 1ml of sterile NSC basal medium. The clumps are dissociated by gently pipetting up and down (3-7 times) until a smooth milky single cell suspension is achieved. The number of pipetting steps directly depends on the size of particles in the minced tissue. Lengthy and vigorous mechanical dissociation should be avoided as it might result in cell death and a reduction in sphere formation.
7. To remove un-dissociated pieces and debris, 10-15 ml of basal medium is added to the tube and the cell suspension is filtered through a 40 micron cell strainer into a 50ml tube.
8. The filtered suspension is centrifuged at 800rpm (110g) for 5min. The supernatant is discarded afterwards.
9. Pelletted cells are then resuspended in 1-2ml of complete NSC medium for cell counting.

3. Cell Count and Plating

1. 10 μL of the cell suspension is added to 90 μL of 0.04% Trypan blue in a 1ml eppendorf tube.
   Note: other appropriate cell dilutions may also be used.
2. Pipette up and down to mix the suspension. 10 μL of the cells/trypan blue mixture is transferred to hemocytometer in order to count cell density.
3. Cells are plated in complete NSC medium (a mixture of NSC basal medium and NSC proliferation supplement at a 9:1 ratio) supplemented with 20ng/ml EGF, 10ng/ml bFGF and 1μl/ml of 0.2% heparin (2μg/ml) in appropriate tissue culture vessels. 5, 20 and 40 ml of medium is used for T25, T80 and T175 flasks, respectively. Antibiotics may be added to the medium at a concentration of 1:100 to decrease chance of contamination.
4. The flask is placed in an incubator set at 37°C and 5% CO₂.

4. Passaging and expansion of GBM derived spheres:

1. When the neurospheres reached an average size of 150-200 μm in diameter, the culture is ready for subculture. The content of each flask is removed and placed in an appropriate size sterile tissue culture tube, and centrifuged at 800 rpm (110 g) for 5 min at room temperature.
2. The supernatant is removed and the pellet is resuspended in 1 ml of %0.05 trypsin-EDTA.
3. To achieve an optimal trypsinization, the cell suspension is incubated at 37°C in a water bath for 2-3 min. To stop the trypsin activity an equal volume of soybean trypsin inhibitor is added to the cell suspension and the cell suspension is gently pipetted up and down.
4. The cell suspension is centrifuged at 800 rpm (110g) for 5 min. Then, the supernatant is removed and the cells are resuspended in 1 ml of NSC medium.
5. A cell count is performed as described earlier.
6. The cells are plated at a concentration of 5x10⁴ cells/ml in complete NSC medium supplemented with growth factors and plated in appropriate size tissue culture vessels as described in previous part.
7. Secondary neurospheres are formed in 7-10 days when incubated at 37° C in a humidified incubator with 5% CO₂.

5. Representative Results:

After plating the single cells harvested from GBM tumor tissue, tumor stem-like cells proliferate and generate small clusters of cells composed of few cells in 3-4 days (see the video and Figure 1). As these clusters grow, they acquire a more spherical shape so that by 7-8 days, proper phase bright spheres with an average diameter of 150-200 microns form (See the video and Figure 2). At higher magnification, healthy spheres usually demonstrate microspikes at their periphery. Having large sphere like clusters in 1-2 days after culture initiation is due to existence of non-dissociated clumps at the binging of the culture and should not be mistaken as true spheres. The amount of debris in primary tumor sphere culture varies depending on the initial source of tissue and whether or not it includes any surrounding brain tissue. Proper tissue preparation techniques including enzymatic and mechanical dissociation, and subsequent filtration of the sample with sufficient amount of medium can result in less debris in culture.

Figure 1. Primary GBM sphere culture 4 days after plating. Tumor stem-like cells proliferate and generate small clusters of cells in 3-4 days. Original Magnification; 20x.

Figure 2. Passage one GBM sphere culture 8 days after plating. Original Magnification; 20x.

Discussion

To isolate neural stem and progenitor cells from normal adult and fetal brains^{1, 2, 3, 4} and also tumor stem-like cells from cancer tissues such as lung⁵, prostate⁶, breast⁷ and brain^{8, 9} the neurosphere assay has been frequently used as the method of choice. Using this simple and reproducible assay, one can generate an indefinite number of cells from resected tumor tissue that show similar characteristics as somatic stem cells; ex vivo multipotency, the ability to create new tumors upon implantation, and self-renewal. These cells could be used to study the basic cancer cell biology including cell-to-cell interactions, and differentiation, migration, invasion and cell death. In addition, isolated tumor stem-like cells provide an invaluable tool to study how tumors form, progress, and relapse and also to unravel the underlying deriving cellular mechanisms that eventually could provide insights to therapeutic options.

Materials

Name	Type	Company	Catalog Number	Comments
NeuroCult NSC Basal Medium (Human)	Medium	Stem Cell Technologies	05750
NeuroCult NSC Proliferation Supplements (Human)	Medium supplement	Stem Cell Technologies	05753
%0.05 trypsin-EDTA	Reagent	GIBCO, by Life Technologies	25300-062
*MEM	Reagent	GIBCO, by Life Technologies	41500-018	HEM component
*HEPES	Reagent	Sigma-Aldrich	H4034	HEM component
*Distilled water	Reagent	GIBCO, by Life Technologies	15230-147
**DNase I	Reagent	Roche Group	104159
**Soybean trypsin inhibitor	Reagent	Sigma-Aldrich	T6522
Pen/Strep	Reagent	GIBCO, by Life Technologies	15140-122
No. 10 scalpel blade	Surgical tool	BD Biosciences	371610
Petri Dish	Culture ware	BD Biosciences	353003
Small forceps	Surgical tools	Fine Science Tools	11050-10
Cell strainer	Sieve	BD Biosciences	352340
T25 flask	Culture ware	Nalge Nunc international	136196
T80 flask	Culture ware	Nalge Nunc international	178905
15 ml tubes	Culture ware	BD Biosciences	352096
50 ml tubes	Culture ware	BD Biosciences	352070
EGF	Growth factor	R&D Systems	2028-EG
b-FGF	Growth factor	R&D Systems	3139-FB
Heparin	Growth factor	Sigma-Aldrich	H4784	Reconstituted in PBS
* To make HEM, mix 1x10L packet of MEM and160ml of 1M HEPES and bring the volume to 8.75 L using distilled water. Set the final PH to 7.4 and store it at 4°C.
** To prepare trypsin inhibitor solution, first make 10 ml of DNase I solution (100 mg DNase dissolved in 100 ml of HEM) and then add 0.14 g of trypsin inhibitor to DNase solution and finally make the volume up to 1 Liter using HEM. Keep aliquots of the final products in -20°C freezer.