Name: determination of sialic acids in liver and milk samples of wild-type and cmah knock-out mice.
Uploaded: 2017-07-14T15:00:00
Description: Watch this Scientific Journal Video about Determination of Sialic Acids in Liver and Milk Samples of Wild-type and CMAH Knock-out Mice. at JoVE.com

This work was supported in part by the Natural Science Foundation of China (grant numbers 31471703, A0201300537 and 31671854 to J.V. and L.L.), and the 100 Foreign Talents Plan (grant number JSB2014012 to J.V.).

Procedures involving animal subjects have been approved by the Ethical Committee of the Experimental Animal Center of Nanjing Agricultural University in accordance to the National Guidelines for Experimental Animal Welfare (Ministry of Science and Technology, PR of China, 2006) with the animals housed in a SPF facility (Permission ID: SYXK-J-2011-0037).
1. Cmah Knock-out Mouse Model
<ol>
	<li>Use wild-type C57Bl/6 mice from the Comparative Medicine Centre of Yangzhou University (Chi...

<ol>
	<li>Lamari, F. N., Karamanos, N. K. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Separation+methods+for+sialic+acids+and+critical+evaluation+of+their+biologic+relevance.">Separation methods for sialic acids and critical evaluation of their biologic relevance.</a> J Chromatogr B Analyt Technol Biomed Life Sci. 781 (1-2), 3-19 (2002).</li><li>Irie, A., Koyama, S., Kozutsumi, Y., Kawasaki, T., Suzuki, A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=The+molecular+basis+for+the+absence+of+N-glycolylneuraminic+acid+in+humans.">The molecular basis for the absence of N-glycolylneuraminic acid in humans.</a> J Biol Chem. 273 (25), 15866-15871 (1998).</li><li>Chou, H. 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The herein presented protocol allows the phenotypical assessment of homozygous Cmah knock-out mice by analyzing and quantifying the relative amounts of Neu5Gc of milk and liver samples. The analysis was performed using a standard HPLC setup with fluorescence detection. The most critical step of this procedure is the preparation of the anion exchange columns and performing the anion exchange chromatography; to settle the resin properly and to collect the right washing and elution fractions takes a bit of practice...

N-acetylneuraminic acid (Neu5Ac) and N-glycolylneuraminic acid (Neu5Gc) are the most common sialic acids in most mammals1. Although able of synthesizing Neu5Ac endogenously, humans are not capable of producing Neu5Gc due to a primary exon deletion on the CMAH gene encoding for a CMP-Neu5Ac hydroxylase2,3. However, animal-based food products can be dietary sources of Neu5Gc4,5,6, leading to the production of anti-Neu5Gc antibodies and therefore trigger an immune response towards Neu5Gc7. This dietary effect of Neu5Gc is suspected to contribute to chronic inflammation and various other diseases8,9,10. In order to comprehensively understand the effects of Neu5Gc in humans, an animal model for the systematic study of the effects of foodborne sialic acids is highly desirable. Although protocols based on polymerase chain reaction (PCR) for analyzing of knock-out mice are well established and a convenient way for the genotypical assessment, the functional analysis of phenotype on the metabolic level requires more specific analysis methods. The phenotype of a Cmah knock-out mouse model can be assessed by isolating and analyzing the composition of sialic acids in liver or milk samples. Several methods for the detection of sialic acids in animal tissues have been reported previously: reacting sialic acids with resorcinol11 or thiobarbituric acid12 result in the formation of a chromophoric product and can be simply analyzed using a platereader based setup, but only the total sialic acid content may be determined. Alternatively, the analysis of sialic acids was also described using gas chromatography13, MALDI-ToF mass spectrometry14 or amperometric methods15. However, the most commonly applied sialic acid analysis methods are based on hydrolytic release, followed by fluorescence derivatization and subsequent high performance liquid chromatography16,17,18.

<table border="0" cellpadding="0" cellspacing="0" width="684">
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		<col />
		<col />
		<col />
		<col />
	</colgroup>
	<tbody>
		<tr height="20">
			<td height="20" style="height:20px;width:147px;">Chemicals:</td>
			<td style="width:144px;"></td>
			<td style="width:143px;"></td>
			<td style="width:251px;"></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">N-acetylneuraminic acid</td>
			<td>Sigma</td>
			<td>A0812</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">N-glycolylneuraminic acid</td>
			<td>Sigma</td>
			<td align="right">50644</td>
			<td>1 mg aliquot should be sufficient</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">o-Phenylenediamine</td>
			<td>Sigma</td>
			<td align="right">694975</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">Sodium hydrogen sulfite</td>
			<td>J&#38;K Scientific Ltd</td>
			<td align="right">75234</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">Tools/Materials:</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">3 mL SPE tubes</td>
			<td>Supelco</td>
			<td>Sigma 57024</td>
			<td>empty solid phase extraction columns</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">Luer stopcock</td>
			<td>Sigma</td>
			<td>S7396</td>
			<td>to stop the flow of the SPE tube</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">Dowex 1X8</td>
			<td>Dow Chemicals</td>
			<td>Sigma 44340</td>
			<td>200-400 mesh</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">Dounce tissue grinder</td>
			<td>Sigma</td>
			<td>D8938</td>
			<td>tight fit</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">HPLC Analysis:</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">High-recovery HPLC vial</td>
			<td>Agilent Technologies</td>
			<td>#5188-2788</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">HPLC System</td>
			<td>Shimadzu</td>
			<td>Nexera</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">Fluorescence Detector for HPLC</td>
			<td>Shimadzu</td>
			<td>RF-20Axs</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">HPLC Column</td>
			<td>Phenomenex</td>
			<td>Hyperclone ODS</td>
			<td>250x4.6 mm</td>
		</tr>
		<tr height="24">
			<td height="24" style="height:24px;">LCMS-grade H2O</td>
			<td>Merck Millipore</td>
			<td>#WX00011</td>
			<td></td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">LCMS-grade Acetonitrile</td>
			<td>Merck Millipore</td>
			<td>#100029</td>
			<td>Hypergrade</td>
		</tr>
		<tr height="20">
			<td height="20" style="height:20px;">Ammonium hydroxide solution</td>
			<td>Fluka</td>
			<td>#44273</td>
			<td>puriss. P.a.</td>
		</tr>
	</tbody>
</table>

determination of sialic acids in liver and milk samples of wild-type and cmah knock-out mice.

CMAH (cytidine monophosphate-N-acetylneuraminic acid hydroxylase) is responsible for the oxidation of cytidine monophosphate-N-acetylneuraminic acids in mammals. However, humans cannot oxidize cytidine monophosphate-N-acetylneuraminic acid to cytidine monophosphate-N-glycolylneuraminic acid due to a primary exon deletion of the CMAH gene. To understand the effects and implications of the lack of CMAH activity in more detail, a Cmah knock-out model in mice is of keen interest in basic and applied research. The analysis method to determine the phenotype of this mouse model is herein described in detail, and is based on the detection of both N-acetylneuraminic acid and N-glycolylenuraminic acid in the liver and milk of wild-type and Cmah knock-out mice. Endogenous sialic acids are released and derivatized with o-phenylenediamine to generate fluorogenic derivatives, which can be subsequently analyzed by HPLC. The presented protocol can be also applied for the analysis of milk and tissue samples from various other origins, and may be of use to investigate the nutritional and health effects of N-glycolylneuraminic acid.

A schematic overview of the described analysis method is shown in Figure 1 and includes the isolation of sialic acids from milk and liver samples of wild-type and Cmah knock-out mutant mice, and the fluorescence derivatization and HPLC analysis of these components. Figure 2 and Figure 3 show representative HPLC chromatograms of derivatized sialic acids of milk and liver samples from homo- an...

Watch this Scientific Journal Video about Determination of Sialic Acids in Liver and Milk Samples of Wild-type and CMAH Knock-out Mice. at JoVE.com

Determination of Sialic Acids in Liver and Milk Samples of Wild-type and CMAH Knock-out Mice.

We describe a HPLC-based method for the determination of N-acetylneuraminic acid and N-glycolylenuraminic acid in mouse liver and milk.

Determination of Sialic Acids in Liver and Milk Samples of Wild-type and CMAH Knock-out Mice.

CMAH (cytidine monophosphate-N-acetylneuraminic acid hydroxylase) is responsible for the oxidation of cytidine monophosphate-N-acetylneuraminic acids in ...

The overall goal of this methodology is the detection of N-Acetylneuraminic acid and N-Glycolylneuraminic acid in the liver and milk of wild-type and CMAH knock-out mice using HPLC analysis. This method can help to answer questions in the field of glycoscience, specifically the effect genotypes of CMAH mouse models have on the actual sialic acid contents of these animals. The main advantage that this technique has in comparison to genetic screens is that relative sialic acid levels can be determined also for heterozygous mice.Evaluating this method will be Cui Cao and Wang Wenjiao, two graduate students from our laboratory. Begin this procedure with collection of mouse milk and mouse liver tissue from CMAH knock-out mice as described in the text protocol. To isolate sialic acids from milk, transfer 50 microliters of milk into a 1.5 milliliter centrifuge tube, and add 1.2 milliliters of prepared aqueous acetic acid solution.To isolate sialic acids from liver tissue, gently thaw 20 to 50 milligram of mouse liver and transfer it into a dounce tissue grinder. Add 1.2 milliliters of the aqueous acetic acid solution and homogenize the tissue by gentle shearing for 10 seconds. Transfer the resulting suspension into a 1.5 milliliter centrifuge tube.Next, incubate the acidified milk or tissue suspension for four hours at 80 degrees Celsius. Then, centrifuge the sample at 14 thousand times g for 10 minutes. Transfer the top 1000 microliters of the supernatant into a fresh 1.5 milliliter centrifuge tube.Remove the solvent by centrifugal evaporation at room temperature to complete dryness. Redissolve the sample in 500 microliters of distilled water. Next, prepare a microanion exchange column by transferring 200 milligrams of anion exchange resin per sample into empty 3 milliliter tubes with an attached stopcock.Add 2 milliliters of the aqueous acetic acid solution to replace the chloride ions in the resin with acetate ion. Close the stopcock as soon as the solvent reaches the top of the resin. Gently add 2 milliliters of distilled water and open the stopcock.Stop the flow as soon as most of the solvent reaches the top of the resin. Make sure that the resin is always covered with solvent. Then, wash the resin column two more times with two milliliters of distilled water for removing the excess acetate.Transfer the resulting 500 microliters of sample solvent onto the resin column and discard the flow-through. Gently was the resin with 2 milliliters of distilled water. Elute the sample anions from the resin using 1 milliliter of a 50 millimolar ammonium acetate solution into a 1.5 milliliter centrifuge tube.Remove the solvent by centrifugal evaporation at room temperature to dryness. Weigh between 5 and 8 milligrams of N-Acetylneuraminic acid on an analytical balance into a 1.5 milliliter centrifuge tube. Note the exact weight and add 164 microliters of distilled water for every milligram.Obtain N-Glycolylneuraminic acid in smaller quantities at a moderate price, such as in 1 milligram aliquots. Add 154 microliters of distilled water directly to compound to obtain a stock solution of approximately 20 millimolar Neu5Gc. Transfer the solution into a 1.5 milliliter centrifuge tube.This solution can be stored at minus 20 degrees Celsius for up to 12 months. Combine 5 microliters from each stock solution into a fresh 1.5 milliliter centrifuge tube. Then, remove the solvent by centrifugal evaporation at room temperature to dryness.Add 20 microliters of the OPD solution to the sialic acid samples derived from mouse milk, mouse liver, or the mixed sialic acid standard. Vortex the sample vigorously for 30 seconds. Then, incubate the samples for four hours at 80 degrees Celsius in the dark.After letting the samples cool down for five minutes, add 80 microliters of distilled water. Then, centrifuge the tubes at 14 thousand times g for one minute. Next, transfer 80 microliters from the supernatant into a 300 microliter high-recovery HPLC vial.The derivitized sialic acid samples can be stored at four to six degrees Celsius for up to one week. Analyze the samples using a standard HPLC system connected to an online fluorescence detector. Use a reversed phase C18 column with a 250 millimeter length and 4.6 millimeter diameter for the analysis.After preparing solvent A and solvent B, and setting up the HPLC run as detailed in the protocol, inject 50 microliters of the sample into the HPLC system. Monitor eluence using the fluorescence detector excitation wavelength of 373 nanometers and an emission wavelength of 448 nanometers. Finally, calculate the relative amount of Neu5Gc as described in the text protocol.Shown here are representative HPLC chromatograms of fluorescence labeled sialic acids from milk samples, derived from homozygous knock-out CMAH mice and heterozygous knock-out CMAH mice. wild-type mice are also shown. Similarly, chromatograms of the mouse liver derived fluorescence labeled sialic acids are shown here.Comparing the relative amounts of Neu5Gc shows that homozygous CMAH knock-out mice contain no Neu5Gc, whereas heterzygous CMAH knock-outs and wild-type mice contain between 10 and 75%Neu5Gc. Once mastered, samples can be prepared within eight hours if the procedure was performed properly. And the samples can be analyzed by HPLC autosampling overnight.While attempting this procedure, it's important to remember to perform the isolation of sialic acid and the derivitization procedure on the same day. Following the procedure, other methods like mass spectrometric analysis can be performed in order to confirm the nature of the obtained fluorescent signals. The development of this technique allows researchers to explore the sialic acid distribution in biological samples.Don't forget that working with concentrated acetic acid and formic acid can be extremely hazardous, and precautions such as wearing protective gear should always be taken while performing this procedure.

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A PCR-based Genotyping Method to Distinguish Between Wild-type and Ornamental Varieties of Imperata cylindrica

Wild-type I. cylindrica (cogongrass) is one of the top ten worst invasive plants in the world, negatively impacting agricultural and natural resources in ...

Do-It-Yourself Device for Recovery of Cryopreserved Samples Accidentally Dropped into Cryogenic Storage Tanks

Liquid nitrogen is colorless, odorless, extremely cold (-196 &deg;C) liquid kept under pressure. It is commonly used as a cryogenic fluid for long term ...

Milk Collection Methods for Mice and Reeves' Muntjac Deer

Animal models are commonly used throughout research laboratories to accomplish what would normally be considered impractical in a pathogen&#8217;s native ...

Sequence-specific Labeling of Nucleic Acids and Proteins with Methyltransferases and Cofactor Analogues

S-Adenosyl-l-methionine (AdoMet or SAM)-dependent methyltransferases (MTase) catalyze the transfer of the activated methyl group from AdoMet to specific ...

Determination of Fatty Acid Oxidation and Lipogenesis in Mouse Primary Hepatocytes

Lipid metabolism in liver is complex. In addition to importing and exporting lipid via lipoproteins, hepatocytes can oxidize lipid via fatty acid ...

Milk Collection in the Rat Using Capillary Tubes and Estimation of Milk Fat Content by Creamatocrit

Milk, as the sole source of nutrition for the newborn mammal, provides the necessary nutrients and energy for offspring growth and development. It also ...