マウス脂肪組織の採取と RNA 解析のための処理

The overall goal of this procedure is to ensure adequate sample collection of white adipose tissue depots from different mice, and to isolate a high amount of good-quality RNA from the tissue. This method can answer key questions in the fields of metabolism, biochemistry and molecular biology that, for example, pertain to gene expression in adipose tissue from treated or genetically-modified mice. The main advantage of this technique is that it allows for the isolation of high amounts of good-quality RNA from adipose tissue which typically has low RNA content.

Demonstrating the procedure will be Emilie Pepin, a research assistant from my laboratory. After euthanizing a mouse, cut the skin over the linea alba according to the text protocol, then make two incisions of approximately two centimeters from the middle of the ribcage towards the right arm and close to the genital organs above the right hind limb. Stretch one corner of the opened skin and use a 22-gauge needle to pin it down on the pad.

Then, pin down the other corner. Using surgical scissors positioned against the skin as flat as possible, carry out blunt dissection of the abdominal subcutaneous fat, or SCF, then transfer it to a precut piece of aluminum foil. Repeat the dissection for the left side of the animal.

Then, pull both the left and right collected fat pads in the aluminum foil and use liquid nitrogen to freeze the sample. To get access to the visceral adipose tissue, cut the abdominal muscle along the linea alba. Then, make an incision in the abdominal muscles from the genitals towards the back of the mouse on both sides.

The fat around the reproductive organs is the perigonadal fat, or PGF. Detach the left and right fat pads from the epididymis, the testes and the ductus deferens and transfer it to the pre-labeled aluminum foil. Then, freeze the sample in liquid nitrogen.

Starting with the left-hand side, expose the kidneys by moving the gut away from the abdominal cavity to the right-hand side. The adipose tissue seen here surrounding the kidney and the adrenal glands is the perirenal fat, or PRF. Isolate and remove the adrenal glands before collecting the PRF.

This can be tedious as they are just a bit pinker than the adipose tissue. Now, isolate the PRF from the back muscular wall and cut the ureter, the renal artery and vein which separates the PRF and kidney from the rest of the body. Then, isolate the PRF from the kidney by cutting and removing the renal capsule.

After isolating the right PRF, transfer the sample to the aluminum foil with the tissue from the left side and use liquid nitrogen to freeze the samples. Chill 1.5-milliliter RNase-free conical tubes, a mortar and pestle and a spatula in liquid nitrogen according to the text protocol. Put the adipose tissue sample in the mortar then use a few layers of brown paper to lift the pestle from the liquid nitrogen and fit it into the mortar.

While holding the pestle with the paper, use the hammer to hit the top of the pestle once or twice. Next, grind the sample using a rotating motion until a fine powder is obtained. Then, remove the pestle, retrieve the spatula from the liquid nitrogen and use it to transfer the sample into the corresponding pre-chilled 1.5-milliliter conical tube.

Dip the spatula back into liquid nitrogen from time to time to prevent the sample from melting. Also, keep the conical tube on dry ice to prevent the sample from thawing. Fill the conical tube to approximately 2/3 capacity with ground sample for adequate RNA yield.

Then, prepare the remaining samples according to the text protocol. Under a chemical hood and while wearing a lab coat, gloves and safety glasses, remove a ground sample from liquid nitrogen. Slowly open the tube, and add 500 microliters of phenol solution.

Close the lid of the tube and vortex at maximum speed for about five seconds, then slowly and carefully open the tube to release the pressure from the nitrogen. The sound of air coming out of the tube will be heard. Pipette an additional 500 microliters of phenol solution into the tube.

Then, vortex and slowly open it as before. Vortex the sample until it is completely dissolved. Then, open the tube to release pressure before processing additional samples.

Once all samples have been processed, briefly vortex them at maximum speed and incubate them at room temperature for five minutes. Centrifuge the tubes at 12, 000 times G and four degrees Celsius for 10 minutes. Then, bring the tubes back to room temperature.

To avoid contamination, for each sample, use a P1000 pipette with a filtered tip to isolate as much RNA as possible from the middle pink layer by piercing the lipid phase near the side of the tube. Dispense the RNA into the new conical tubes without touching the sides of the tubes to prevent transferring lipids present on the outside of the tip. Add 200 microliters of pure chloroform to each sample and mix the tubes by inversion for 15 seconds.

Then, after incubating the samples at room temperature for 10 minutes, centrifuge the tubes at 12, 000 times G and four degrees Celsius for 15 minutes and bring the tubes back to room temperature. For each sample, use a P1000 pipette and filtered tips to transfer as much aqueous transparent RNA-containing top phase as possible to the second set of corresponding conical tubes. Next, add 500 microliters of 100%isopropanol to each sample and mix the tubes by inversion for 15 seconds.

Then, incubate the samples at room temperature for 10 minutes. Centrifuge the tubes at 12, 000 times G and four degrees Celsius for 10 minutes before bringing the tubes back to room temperature. Discard the isopropanol by pouring it out of each tube.

Now, add one milliliter of 75%ethanol to each sample and briefly vortex the tubes at maximum speed. Then, centrifuge the samples at 7, 500 times G and four degrees Celsius for five minutes. After spinning the samples and bringing them to room temperature, discard the 75%ethanol by inverting each tube and lighting tapping them against brown paper to remove any residual ethanol.

Leave the lid open and air-dry the RNA pellet for about 15 to 20 minutes. After evaluating the size of the RNA pellets, add 10 to 25 microliters of RNase-free water to each sample. Incubate the samples in a heat block at 60 degrees Celsius for five minutes.

Then, briefly vortex the tubes. Incubate the samples in the same heat block for an additional five minutes. Then, quickly spin all the samples and immediately place them on ice.

Carry out RT-PCR for gene expression in adipose tissue according to the text protocol. As expected, mice on the high fat diet had increased body weight and weight gain compared to litter mates on the normal diet. These observations were accompanied by a more than two-fold increase in the weight of the PGF, PRF and SCF in obese mice compared to those on the normal diet.

This table shows that for each white adipose tissue, RNA isolation by phenol solution produced samples with an OD260 over OD280 of around 2.0 which is considered pure for RNA. As seen in this bar graph, realtime PCR data showed that leptin mRNA expression was significantly higher in PGF, PRF and SCF of obese mice compared to those on a normal diet. The differences observed in leptin mRNA expression were not due to a variation of s16, the reference gene used to normalize the results between the two groups of mice as CT values were not altered.

Once mastered, this technique can be done in four hours if it is performed properly. While attempting this procedure, it's important to remember to work in an RNase-free environment during the RNA extraction procedure. Following this procedure, other methods like realtime PCR amplification can be performed in order to answer additional questions like gene expression modifications.

After its development, this technique paved the way for researchers in the field of metabolism to explore adipose tissue modulations related to obesity and diabetes in rodents. After watching this video, you should have a good understanding of how to isolate different fat pads and isolate RNA from them. Don't forget that working with the phenol solution can be extremely hazardous, and precautions such as wearing a lab coat and gloves should always be taken while performing this procedure.