Lipid-Mediated Transfection of Human Astrocytes

Introduction

Astrocytes are by far the most numerous cell type in the central nervous system (CNS) and have critical roles in adult CNS homeostasis. They provide biochemical and nutritional support of neurons and endothelial cells which form the blood-brain barrier, perform the vast majority of synaptic glutamate uptake, and maintain extracellular potassium levels (Rothstein et al., 1996; Rothstein et al., 1994). Although there are few known differences between cortical and hippocampal astrocytes, it has been reported that astrocytes from different regions of the brain show a differential sensitivity to ischemic injury (Xu et al., 2001; Zhao & Flavin, 2000).


The following protocols provide instructions for lipid-mediated transfection of plasmid DNA or siRNA into GIBCO® Human Astrocytes using the Lipofectamine® LTX Reagent or the Lipofectamine RNAiMax Reagent. Lipofectamine® LTX Reagent is a proprietary, animal-origin free formulation for the transfection of DNA into eukaryotic cells with low cytotoxicity. Lipofectamine® RNAiMAX is a proprietary formulation specifically developed for the transfection of siRNA and Stealth™ RNAi duplexes into eukaryotic cells.

Required Materials

  • GIBCO® Human Astrocytes (Cat. no. N7805-100)
  • GIBCO® Astrocyte Medium (Cat. no. A12613-01) Note: The medium kit includes N-2 Supplement, 100X (Cat . no. 17502-048), Dulbecco’s Modified Eagle Medium (D-MEM) (1X), liquid (Cat. no. 10569-010), and One Shot™ Fetal Bovine Serum (FBS), Certified (Cat. no. 16000-077).
  • Dulbecco’s Phosphate-Buffered Saline (D-PBS) (1X), liquid without Ca2+ and Mg2+ or phenol red (Cat. no. 14190-144)
  • Dulbecco’s Phosphate-Buffered Saline (D-PBS) (1X), liquid with Ca2+ and Mg2+
  • (Cat. no. 14040-133)
  • Geltrex™ Reduced Growth Factor Basement Membrane Matrix (Cat. no. 12760)
  • StemPro® Accutase® Cell Dissociation Reagent (Cat. no. A11105)
  • Opti-MEM® I Reduced Serum Medium (Cat. no. 31985-062)
  • Appropriate tissue culture plates and supplies

For transfecting plasmidDNA

  • Plasmid DNA of interest (100 ng/μL or higher)
  • Lipofectamine® LTX Reagent and PLUS™ Reagents (Cat. no. 15338-100)

For transfecting siRNA

  • Silencer® Select siRNAs (see www.invitrogen.com for ordering information)
  • Lipofectamine® RNAiMAX Transfection Reagent (Cat. no. 13778-075 or 13778-150)

TOP

Ordering Information

Sku Name Size Price Qty
17502048 N-2 Supplement (100X) 5 mL USD 70.00
10569010 DMEM, high glucose, GlutaMAX™ Supplement, pyruvate 500 mL USD 26.40
16000077 Fetal Bovine Serum, certified, One Shot™ format, US origin 50 mL USD 48.00
14190144 DPBS, no calcium, no magnesium 500 mL USD 18.35
14040133 DPBS, calcium, magnesium 500 mL USD 18.35
A1110501 StemPro® Accutase® Cell Dissociation Reagent 100 mL USD 37.60
31985062 Opti-MEM® I Reduced Serum Medium 100 mL USD 18.30
15338100 Lipofectamine® LTX Reagent with PLUS™ Reagent 1 mL USD 520.00
13778075 Lipofectamine® RNAiMAX Transfection Reagent 0.75 mL USD 393.26

Important Guidelines for Lipid-Mediated Transfection

Follow these important guidelines when performing lipid-mediated transfections of human astrocytes.

  • Maintain human astrocytes on Geltrex™-coated plates.
  • Adding antibiotics to media during transfection may result in cell death. If you wish to use antibiotics during transfection, test your conditions thoroughly.
  • Maintain the same seeding conditions between experiments. Use low-passage cells; make sure that cells are healthy and greater than 90% viable before transfection.
  • Transfections can be performed both in the presence or absence of serum. Test serum-free media for compatibility with Lipofectamine® LTX or Lipofectamine® RNAiMAX Reagent.
  • Using PLUS™ Reagent enhances transfection performance in human astrocytes.
  • We recommend Opti-MEM® I Reduced Serum Medium to dilute the DNA and Lipofectamine® LTX Reagent or the siRNA and Lipofectamine® RNAiMAX Reagent before complexing.
TOP

Preparing Geltrex™-Coated Plates for Human Astrocytes

Before thawing or passaging GIBCO® Human Astrocytes, prepare culture vessels coated with Geltrex™ as described below.

  1. Thaw a bottle of Geltrex™ Basement Membrane Matrix at 4°C overnight.

  2. On ice, prepare a stock solution of Geltrex™ diluted 1:1 in D-MEM. Store in aliquots at –20°C until needed.

  3. Dilute the stock solution 1:100 in D-MEM and coat the bottom of each culture vessel (200 μL of Geltrex™ per cm2 of culture vessel).

  4. Incubate the culture vessel at 37°C for 1 hour. Dishes coated with Geltrex™ can be used immediately or stored at 4°C for up to a week, sealed with Parafilm®. Do not allow dishes to dry. When you are ready to add cells, aspirate the Geltrex™ solution and rinse the plates once with D-PBS with Ca2+ and Mg2+ before adding the cell solution.
TOP

Preparing Media

Aseptically mix the following components for preparing 100 mL of complete GIBCO® Astrocyte Medium. Complete Astrocyte Medium is stable for 2 weeks when stored at 4°C protected from light.

Component Amount per 100 mL Amount per 500 mL
D-MEM89 mL445 mL
N-2 Supplement1 mL5 mL
FBS10 mL50 mL


  
Note:  Adding EGF at a final concentration of 20 ng/mL can increase proliferation, but may result in morphological and phenotypic changes in human astrocytes.

TOP

Handling and Harvesting Human Astrocytes

  1. Warm Complete Astrocyte Medium and StemPro® Accutase® Cell Dissociation Reagent in a 37°C water bath before use.

  2. Transfer conditioned medium from the cells to a new tube; this will be used to stop the enzyme reaction in step 6.

  3. Wash cells once with 1X D-PBS without calcium, magnesium, or phenol red.

  4. Aspirate D-PBS and add StemPro® Accutase® to the cells.

  5. Incubate for 5–10 minutes at 37°C. Rock the cells every ~5 minutes and check under a microscope for detachment and dissociation toward single cells.

  6. When the cells have detached, add an equal volume (1:1) of conditioned medium (from Step 2) to slow the Accutase® activity.

  7. Transfer the cells to a 15-mL or 50-mL tube.

  8. Rinse culture vessels with complete medium and add it to the tube.

  9. Centrifuge the tube for 4 minutes at 200 × g.

  10. Aspirate and discard the supernatant.

  11. Gently resuspend the pellet in Complete Astrocyte Medium.

  12. Count the live cells using a method of choice.

  13. To replate human astrocytes, remove a Geltrex™-coated plate from 4°C storage and tip slightly to aspirate the Geltrex™ solution. Rinse the plate once with D-PBS with calcium and magnesium. Do not allow the plate to dry out.

  14. Immediately seed the astrocytes at the desired concentration (we recommend ≥2 × 104 cells/cm2).

  15. Incubate the cells in an incubator at 37°C in a humidified atmosphere (90%) of 5% CO2 in air. Change the medium every 2–3 days with fresh Complete Astrocyte Medium.
TOP

Transfecting Plasmid DNA into Human Astrocytes Using Lipofectamine® LTX Reagent

Use this procedure to transfect plasmid DNA into GIBCO® Human Astrocytes using the Lipofectamine® LTX Reagent in a 24-well format (for other formats, see Scaling Up or Down Transfections, below). All amounts and volumes are given on a per well basis.

  1. The day before transfection, prepare Human Astrocytes that have recovered from cryopreservation and have reached 80% confluency. Use StemPro® Accutase® to detach the cells and count the cells. Plate 5 × 104 cells per well in 0.5 mL of complete growth medium. Cell density should be 80–90% confluent on the day of transfection.
  2. For each well of cells to be transfected, dilute 0.5 μg of DNA into 100 μL of Opti-MEM® I Reduced Serum Medium without serum.
  3. Using PLUS™ Reagent: Mix PLUS™ Reagent gently before use, then add 0.5 μL PLUS™ Reagent (a 1:1 ratio to DNA) directly to the diluted DNA. Mix gently and incubate for 5–15 minutes at room temperature.
  4. For each well of cells, dilute 1.5–3.0 μL of Lipofectamine® LTX into the above diluted DNA solution, mix gently and incubate for 25 minutes at room temperature to form DNA-Lipofectamine® LTX complexes.
  5. Remove growth medium from cells and replace with 0.5 mL of complete growth medium. Add 100 μL of the DNA-Lipofectamine® LTX complexes directly to each well containing cells and mix gently by rocking the plate back and forth.
  6. Complexes do not have to be removed following transfection. Incubate the cells at 37°C in a CO2 incubator for 18–24 hours post-transfection before assaying for transgene expression.


Scaling Up or Down Transfections

To transfect Human Astrocytes in different tissue culture formats, vary the amounts of Lipofectamine® LTX Reagent, DNA, cells, medium and PLUS™ Reagent used in proportion to the relative surface area, as shown in the table (amounts given on a per well basis).

 

Culture
vessel
Surface area
per well*
Volume
of plating
medium
Cells per
well
Volume of
dilution
medium†
 
DNA

Lipofectamine®
LTX Reagent

PLUS™
Reagent

96-well
 0.3 cm2 100 μL1.0 × 10420 μL100 ng0.3–0.6 μL 0.1 μL
48-well1 cm2200 μL2.0 × 104 40 μL200 ng0.6–1.2 μL 0.2 μL
24-well2 cm2500 μL 5.0 × 104100 μL500 ng1.5–3.0 μL0.5 μL
12-well4 cm21 mL 1.0 × 105200 μL1 μg3.0–6.0 μL1.0 μL

 6-well

 10 cm2

 2 mL

 2.5 × 105

500 μL
 
2.5 μg
7.5–15.0 μL 2.5 μL  



* Surface areas may vary depending on the manufacturer.
If the volume of Lipofectamine® LTX Reagent is too small to dispense accurately, and you cannot pool dilutions, predilute Lipofectamine® LTX Reagent 10-fold in Opti-MEM® I Reduced Serum Medium, and dispense a 10-fold higher amount (should be at least 1.0 μl per well). Discard any unused diluted Lipofectamine® LTX Reagent.

TOP

Transfecting siRNA into Human Astrocytes Using Lipofectamine® RNAiMAX Reagent

Prepare siRNAs

  1. Resuspend the Silencer® Select siRNAs with nuclease-free water. A convenient stock concentration is 100 μM, which can be diluted to meet downstream experimental needs.
  2. Validate the concentration of the siRNA by measuring absorption at 260 nM using a spectrophotometer and adjust with water if necessary. Keep aliquots frozen at –20°C.
  3. Dilute stock siRNAs of 100 μM to a working concentration of 10 μM.
  4. From the working stock dilute siRNAs in 20 μL of Opti-MEM® I per well to achieve a final concentration of 30 nM or your desired concentration (1 nM–100 nM) in tubes or plates. When applicable, make master mixes for replicates to minimize variability (at least one well overage). For example with a 10 μM siRNA stock, mix 0.39 μL of siRNA (3.9 pmols) + 19.61 μL of Opti-MEM®-I per well or 1.56 μL of siRNA + 78.44 μL of Opti-MEM®-I for the master mix.
  5. Plate siRNAs in a Geltrex™-coated plate using the proper method for coating as provided by the manufacturer


Prepare cells

Culture cells according to manufacturer’s cell protocol. Cells were in culture for about a week. On the day of transfection, harvest cells according to the protocol. Count and dilute cells to the proper density. We recommend performing an initial optimization experiment to determine your optimal cell density. Based on our optimization, we found 4,000 cells per well to be an optimal cell density.

Transfect cells

We recommend performing an initial optimization experiment to determine the optimal amount of transfection agent to add that balances good knockdown and low toxicity. Based on our optimizations, we found 0.15 μL per well of Lipofectamine® RNAiMAX to be the best condition.

  1. Dilute 0.15 μL per well of Lipofectamine® RNAiMAX in Opti-MEM® I for a total volume of 10 μL per well in a polystyrene 12 × 75-mm tube or a conical centrifuge tube. Make a master mix of sufficient volume to treat all wells to be transfected plus an extra 10% for pipetting variability. Mix the Lipofectamine® RNAiMAX–Opti-MEM® I mixture by gently flicking the bottom of the tube.
  2. Combine 10 μL of the Lipofectamine® RNAiMAX–Opti-MEM® I mixture per 20 μL of diluted and pre-plated siRNA. Mix by tapping the plate back and forth. Incubate this mixture for 10 minutes at room temperature.
  3. After the incubation, add 80 μL of human astrocytes that have been diluted to the proper density to each well. The final volume per well should be 110 μL per well.
  4. Place the plate in a 37°C incubator under normal cell culture conditions. Remove the cells and assay for the expression levels of the gene of interest at the desired time point (typically 24–48 hours post-transfection).
TOP

References

  1. Rothstein, J.D., Dykes-Hoberg, M., Pardo, C.A., Bristol, L.A., Jin, L., Kuncl, R.W., et al. 1996. Knockout of glutamate transporters reveals a major role for astroglial transport in excitotoxicity and clearance of glutamate. Neuron 16:675–686.

  2. Rothstein, J.D., Martin, L., Levey, A.I., Dykes-Hoberg, M., Jin, L., et al. 1994. Localization of neuronal and glial glutamate transporters. Neuron 13:713–725.

  3. Xu, L., Sapolsky, R.M., and Giffard, R.G. 2001. Differential sensitivity of murine astrocytes and neurons from different brain regions to injury. Exp Neurol. 169:416–424.

  4. Zhao, G., and Flavin, M. P. 2000. Differential sensitivity of rat hippocampal and cortical astrocytes to oxygen-glucose deprivation injury. Neurosci Lett. 285:177–180.
TOP
LT158                    17-Mar-2011