This work was supported by the US National Institutes of Health grant R01DK126944 to S.M.R.

The use of all animals was approved by the Institutional Animal Care and Use Committee (IACUC) at Weill Cornell Medical College of Cornell University.
1. Preparation of buffers and collection plates
<ol>
	<li>Make 5% bovine serum albumin (BSA) by dissolving 5 g of BSA in 100 mL of Dulbecco&#39;s modified Eagle&#39;s medium (DMEM) without phenol red. Gently stir the BSA to dissolve (shaking is counterproductive). Once the BSA is fully dissolved, filter-sterilize the media with a 0.2 &#181;m filter. Store the BSA media at 4 &#176;C for up to 1 month.</li>
	<li>Make working concentrations of control and stimulation media. Control media: 5% BSA media with vehicle control. Stimulation media: 5% BSA media with 0.5 &#181;M CL-316,243. Make fresh stimulation media for each experiment.</li>
	<li>Warm the media to be used to 37 &#176;C. Label a 96-well plate for media collection.</li>
</ol>
2. Sample preparation
<ol>
	<li>Perform cell culture as described below. Undertake all cell work in a sterile fume hood to minimize outside contamination.
	<ol>
		<li>Isolate and differentiate primary preadipocytes, as in73,74.
		<ol>
			<li>Plate primary preadipocytes at a high density, such as 1 x 105 cells/well in a 24-well plate in 1 mL/well culture media (15% fetal bovine serum (FBS) and 1x penicillin-streptomycin-glutamine in DMEM/F12).</li>
			<li>After the cells reach 100% confluency, differentiate with 5 &#181;M dexamethasone, 0.5 mM 3-isobutyl-1-methylxanthine, 1 &#181;g/mL insulin, and 1 &#181;M thiazolidinedione (TZD) in culture media for 3 days. Then, change to culture media with 1 &#181;g/mL insulin for at least 3 days to grow lipid droplets. Use 1 mL/well of media in the 24-well plate.</li>
			<li>Change the culture media (1 ml/well) with insulin every 2 or 3 days. The cells can be maintained in media with insulin for up to 2 weeks. Use only cultures in which differentiation rates are over 90% and are similar across groups for this assay, as reduced differentiation could be misinterpreted as a reduction in lipolytic rate.</li>
			<li>Culture the cells in insulin free media for 24 h prior to measuring lipolysis. 
			NOTE: Insulin in the media maintains lipid droplets, but also inhibits lipolysis. Incubation without insulin for 24 h allows for full lipolytic activation without a loss of lipid droplet volume. In some systems, the culture time without insulin may need to be shortened or extended.</li>
		</ol>
		</li>
		<li>Wash the cells with DPBS once to remove residual serum from the culture media. 
		NOTE: This protocol does not include serum starvation, which can activate lipolysis. Serum starvation may be employed at the researcher&#39;s discretion.</li>
	</ol>
	</li>
	<li>Perform ex vivo culture as described below.
	<ol>
		<li>Prepare a 6-well plate, with one well for each tissue to be collected from each mouse. Place 4 mL of room temperature DMEM in each well to be used. 
		NOTE: BSA in the collection media is not necessary.</li>
		<li>Prepare a 48-well plate for the lipolysis assay, with one well for each replicate. Place 400 &#181;L of room temperature DMEM in each well to be used. Use two to four control and two to four stimulated wells per tissue per mouse.</li>
		<li>Euthanize the mouse by cervical dislocation under anesthesia, with a secondary method such as bilateral pneumothorax. Here, we used a 32 g, 7-month-old female C57BL/6J mouse, fed with a 45% high fat diet for 4 months. 
		NOTE: This protocol can also be used for males, as well as other strains, diets, and ages.</li>
		<li>Spray with 70% ethanol and use scissors to make a small (~ 1 cm) lateral incision at the center of the abdominal skin, pull the skin apart by pinching either side with thumb and forefinger and fold the lower abdominal skin over to reveal the posterior subcutaneous depots. Locate and remove the inguinal lymph node and blunt dissect the inguinal adipose tissue immediately posterior to the inguinal lymph node using forceps.</li>
		<li>To collect the gonadal adipose tissue, make a lateral and a vertical incision in the peritoneum to access the peritoneal cavity. Hold the gonadal fat pad with tweezers and cut along the uterus (or epididymis for males) to remove the gonadal adipose tissue. Place the collected depots into a 6-well plate.</li>
		<li>Remove the tissue from well, place on a silicone mat, and cut into 5 to 7 mg chunks with scissors.</li>
		<li>Weigh out 25 to 30 mg (five or six chunks) for each assay well and place into a 48-well assay plate. Blot the tissue on a clean towel before weighing to remove any media. Weigh the weight boat after removal of the tissue and record the weight of any residue left behind. Wipe the weight boat clean between samples and re-tare if necessary. Use a new weight boat for each tissue.</li>
		<li>Once all the tissue samples have been weighed, place the 48-well assay plate in a 37 &#176;C, 10% CO2 incubator for 15 min.</li>
	</ol>
	</li>
</ol>
3. Lipolysis assay
<ol>
	<li>Perform media collection. Undertake transfer of the media and subsequent sample collection in a sterile fume hood to minimize potential contamination from outside sources.
	<ol>
		<li>At t = 0, remove the media and add 400 &#181;L per well of control or stimulation media, and place assay the plate into a 37 &#176;C, 10% CO2 incubator. For ex vivo tissue culture, carefully remove media using a pipette; suction should never be used. 
		NOTE: Alternatively, prepare a second plate with control and stimulation media, and transfer the tissues.</li>
		<li>At t = 1, 2, 3 and 4 h, collect 200 &#181;L of media, replace with 200 &#181;L of the appropriate control or stimulation media, and return the assay plate to the incubator. Store the collection plate at 4 &#176;C. To determine the FFA buffering capacity of the BSA media, use an additional collection at 24 h. 
		NOTE: The experiments can be stopped here, and the collected media can be stored at -20 &#176;C.</li>
	</ol>
	</li>
</ol>
4. FFA colorimetric assay
<ol>
	<li>Warm the reagents to room temperature and dissolve one bottle of color reagent A with one bottle of solvent A, and one bottle of color reagent B with one bottle of solvent B. From the date of reconstitution, these reagents are best used within 1 week. Discard 1 month after reconstitution.</li>
	<li>Thaw and mix the samples.</li>
	<li>Create an FFA standard curve. The standard solution is 1 mM. Use the following volume with the reagents for the standard curve: 25 &#181;L, 20 &#181;L, 15 &#181;L, 10 &#181;L, 10 &#181;L (1:2 dilution), 10 &#181;L (1:4 dilution), 10 &#181;L (1:8 dilution), and 10 &#181;L water for maximal range. For low FFA levels, 10 &#181;L of 1 mM, 0.8 mM, 0.6 mM, 0.4 mM, 0.2 mM, 0.1 mM, and 0.05 mM standard may be more applicable.</li>
	<li>Pipette standards and samples into a 96-well assay plate. The recommended sample volume is 10 &#181;L. Include three wells with the same volume of BSA media as the samples for background correction. 
	NOTE: If sample concentrations fall outside the range of the standard curve, repeat the assay, adjusting the sample volume to&#160;2-25 &#181;L.</li>
	<li>Add 150 &#181;L of reagent A to each well and mix. Avoid generating bubbles. Pop any bubbles with a fine gauge needle. Incubate the assay plate at 37 &#176;C for 5 min.</li>
	<li>Read the absorbance of the plate at 550 nm and 660 nm reference (Reading A).</li>
	<li>Add 75 &#181;L of reagent B to each well and mix. Avoid generating bubbles. Pop any bubbles with a fine gauge needle. Incubate the assay plate at 37 &#176;C for 5 min.</li>
	<li>Read the absorbance of the plate again at 550 nm and 660 nm reference (Reading B).</li>
</ol>
5. Glycerol colorimetric assay
<ol>
	<li>Reconstitute the free glycerol reagent with 36 mL of ultrapure water and acclimatize to room temperature. These reagents are best used within a few weeks. Discard 2 months after reconstitution.</li>
	<li>Thaw and mix the samples.</li>
	<li>Create a glycerol standard curve by making a seven point, 2-fold serial dilution of the glycerol standard solution and a water blank. 
	NOTE: The standard curve is relatively linear up to 25 &#181;L of 2.8 mM glycerol, but not linear at higher concentrations.</li>
	<li>Pipette 25 &#181;L each of standard and samples into the 96-well assay plate. Include three wells with the BSA media for background correction.</li>
	<li>Add 175 &#181;L of free glycerol reagent to each well and mix. Avoid generating bubbles. Pop any bubbles with a fine gauge needle. Incubate the assay plate at 37 &#176;C for 5 min.</li>
	<li>Read the absorbance of the plate at 540 nm.</li>
</ol>
6. Calculation of lipolytic rate
<ol>
	<li>Start with optical density (OD) values. For glycerol, use A540 OD values directly.&#160;Calculate the OD of the FFA assay according to the following formula: 
	OD = (Reading B: A550 - A660) - (Reading A: A550 - A660)</li>
	<li>Use the standard curve to calculate the FFA and glycerol levels in the collected samples. Plot the standard OD values on the y-axis, and on the x-axis, use standard concentrations relative to the sample volume (i.e., the concentration of the wells with 20 &#181;L of 1 mM FFA standard on a plate with 10 &#181;L samples is equal to 2 mM). Fit a linear trendline: 
	y = mx + b</li>
	<li>Visually inspect the standard curve and remove any points outside the linear range of the assay. Calculate sample concentrations using the equation: 
	Sample concentration: x = (OD - b)&#160;&#247; m</li>
	<li>Adjust and re-assay samples falling outside the linear assay range. To get the final sample concentration, subtract the concentration of the background wells containing only BSA media from the concentration of the samples.</li>
	<li>Calculate the moles of FFA and glycerol produced by each sample at each time point, according to the formula: 
	<img alt="Equation 1" src="/files/ftp_upload/65106/65106eq01.jpg" style="margin: auto;" /> 
	where Cn = concentration at time t = n; Vt = total volume in the well; Vs = sample collection volume; and Mn = moles produced at time t = n (when concentrations are in mM and volumes are in mL the output is &#181;Mol). 
	For examples, at various time points: 
	M1 = C1&#160;&#215; Vt 
	M4 = C4&#160;&#215; Vt + (C1 + C2+ C3)Vs 
	or 
	M4 = C4&#160;&#215; Vt + C3&#160;&#215; Vs + C2&#160;&#215; Vs + C1&#160;&#215;Vs</li>
	<li>Normalize to tissue weight by dividing by the tissue weight for each sample in grams to obtain units of &#181;mol/g. For cultured cells, values are presented as &#181;mol/well. Ensure that the cell number and differentiation efficiency are comparable from well to well. 
	NOTE: Differences in proliferation or differentiation efficiency will complicate the interpretation of results and require another method of normalization (e.g., normalization to protein; see discussion).</li>
	<li>Calculate the slope of the &#181;mol/g produced (y-axis) versus time (x-axis) for each sample individually.
	<ol>
		<li>In a spreadsheet, this can be done using the =SLOPE(known_ys,known_xs) function. In a new cell, type &#34;=SLOPE&#34; (then use the cursor to highlight the sample glycerol or FFA values in &#181;mol/g, then to highlight the corresponding time values).</li>
		<li>Verify the linearity of the data. R2 values are a quick way to determine linearity of the samples. In a spreadsheet, this can be done using the =RSQ(known_ys,known_xs) function, in the same manner as described in step 6.7.1, but the initial input is =RSQ. Ensure that the R2 values are &#62; 0.98; lower values indicate deviation from linearity. This can result from a measurement/sampling error or loss of linearity.
		<ol>
			<li>Another way to test linearity is to perform a linear regression for each sample and plot the residuals. In a statistical analysis software, generate an XY table with a single Y value for each time point. Select Analyze &#62; Simple linear regression and select the box for Residual Plot before hitting OK. The residual plot will appear as a new graph.</li>
		</ol>
		</li>
	</ol>
	</li>
	<li>Use the FFA and glycerol production rate (i.e., slope [(&#181;mol/g/h]) for each sample as an individual data point to perform statistical analysis, and plot values if different lipolytic conditions are being compared. If lipolytic rates are being compared across genotypes, use two or three samples per animal as technical replicates, and use the average for one data point per animal, so that the sample size is equal to the number of animals.</li>
</ol>

The authors have nothing to disclose.

Here, we provide a basic protocol for measuring the rate of lipolysis in adipocytes and ex vivo adipose tissue. To quantify lipolysis, it is important to measure lipolytic rate in the linear phase. We use a serial sampling technique, where a large fraction of media is collected and replaced with fresh media at regular intervals. This semiconservative method allows for the addition of fresh BSA with FFA buffering capacity and delays feedback inhibition, extending the duration of linear lipolysis. This experimenta...

Excess nutrients are stored in white adipose tissue in the form of triglycerides in the neutral lipid core of lipid droplets. Triglyceride stores are mobilized via lipolysis, a process by which the fatty acid side chains are sequentially cleaved by adipose tissue triglyceride lipase (ATGL), hormone-sensitive lipase (HSL), and monoglyceride lipase (MGL), resulting in the release of free fatty acids (FFAs) and the glycerol backbone1,2. Lipolysis is activated by catecholamine signaling in the adipose tissue. Sympathetic nerve terminals locally release catecholamines, which bind to &#946;-adrenergic receptors on the adipocyte plasma membrane. Upon ligand binding, these G-protein coupled receptors (GPCRs) activate adenylyl cyclase via G&#945;s. Subsequent activation of protein kinase A (PKA) by cAMP results in the upregulation of both ATGL and HSL. The phosphorylation of perilipin-1 by PKA causes the dissociation of ABHD5 (also known as CGI-58), which binds and coactivates ATGL3. PKA directly phosphorylates HSL, promoting its translocation from the cytosol to the lipid droplet, where interaction with phosphorylated perilipin-1 further promotes its lipase activity4,5,6,7. The third lipase involved in lipolysis, MGL, does not appear to be regulated by catecholamine signaling8. Importantly, triglyceride synthesis in adipocytes is mediated by the glycerol lipid synthesis pathway, which does not involve the formation of monoglycerides as an intermediate; instead, glycerol-3-phosphate acyl transferases catalyze the formation of lysophosphatidic acid, which is combined with another fatty acyl-CoA to form phosphatidic acid, and then isomerized to diglycerides before the final synthesis of triglycerides (Figure 1)9,10,11.
<img alt="Figure 1" class="xfigimg" src="/files/ftp_upload/65106/65106fig01.jpg" /> 
Figure 1: Lipolysis and glycerol lipid synthesis pathways. Top: Lipolytic pathway; enzymes shown in red: adipose tissue triglyceride lipase (ATGL), hormone sensitive lipase (HSL), and monoglyceride lipase (MGL). Bottom: glycerol lipid synthesis pathway; enzymes shown in green: diglyceride acyltransferase (DGAT), phosphatidic acid phosphatase (PAP), lysophosphatidic acid acyltransferase (LPAT, also known as LPAATs), and glycerol-3-phosphate acyltransferase (GPAT). Lipids: triglyceride (TG), diglyceride (DG), monoglyceride (MG), free fatty acid (FFA), fatty acyl-CoA (FA-CoA), lysophosphatidic acid (LPA), and phosphatidic acid (PA). Other metabolites: inorganic phosphate (Pi) and glycerol 3-phosphate (G3P). <a href="https://www.jove.com/files/ftp_upload/65106/65106fig01large.jpg" target="_blank">Please click here to view a larger version of this figure.</a>
Extracellular adenosine is another important regulator of lipolysis, working through Gs- and Gi-coupled GPCRs to impact adenyl cyclase activity. The predominant adenosine receptor in adipocytes, ADORA1, inhibits adenylyl cyclase, and thus lipolysis through the activation of Gi12. Expressed at lower levels, and primarily in brown adipocytes, ADORA2A activates lipolysis via Gs signaling13. ADORA1 impacts both basal lipolysis and the response to adrenergic agonists. The effect of adenosine on lipolysis can be controlled by adding adenosine deaminase to neutralize adenosine, as well as the ADORA1-specific agonist phenylisopropyladenosine14,15. Hormonal activation of Gq-coupled GPCRs can also affect lipolysis via the activation of phospholipase C and protein kinase C16,17,18,19. Inflammatory signals also impact lipolytic rates. TLR4 activation by LPS (and other endotoxins) increases the lipolytic rate by activating ERK, which phosphorylates perilipin-1 and HSL20. TNF-&#945; also activates lipolysis via ERK and NF-&#954;B activation, as well as transcriptional downregulation of the phosphodiesterase PDE-3B and CIDEC21,22,23. IL-6 has also been associated with increased adipocyte lipolysis, especially in mesenteric adipose tissue, whose FFA release impacts hepatic steatosis and gluconeogenesis24,25,26.
Lipolysis is suppressed during the fed state by insulin. AKT phosphorylates and activates PDE-3B to suppress cAMP signaling and prevent PKA activation27. Insulin also transcriptionally downregulates ATGL28. Obesity promotes catecholamine resistance through a variety of mechanisms, including the downregulation of &#946;-adrenergic receptors in adipocytes29,30,31,32,33. Adipocytes express all three &#946;-adrenergic receptors (&#946;-1, &#946;-2, and &#946;-3). While &#946;-1 and &#946;-2 adrenergic receptors are ubiquitously expressed, the &#946;-3 adrenergic receptor is predominately expressed in adipocytes in mice34,35. Adrb3 expression is induced by C/EBP&#945; during adipogenesis36. The &#946;-3 adrenergic receptor is highly expressed in mature adipocytes. The activation of &#946;-1 and &#946;-2 adrenergic receptors is self-limiting due to feedback inhibition by &#946;-arrestin37. Feedback inhibition of the &#946;-3 adrenergic receptor is mediated by other signaling pathways, which reduce Adrb3 expression33,38,39.
Numerous compounds can be used to activate adipocyte lipolysis. Catecholamines are major physiological activators of lipolysis. Norepinephrine (or noradrenaline) and epinephrine (or adrenaline) activate all three &#946;-adrenergic receptors40. Norepinephrine and epinephrine also effect lipolysis via activation of &#945;-adrenergic receptor signaling41. Commonly used &#946;-adrenergic receptor agonists include isoproterenol, which is a non-selective &#946;-adrenergic receptor agonist, and the &#946;-3 adrenergic receptor agonists CL-316,243 and mirabegron42. Given that adipocytes predominantly express the &#946;-3 adrenergic receptor, we use CL-316,243 as an example here. Its specificity for the &#946;-3 adrenergic receptor also makes it a relatively specific activator of adipocyte catecholamine signaling, that can also be safely used in vivo. Note that the commonly used concentration of 10 &#181;M CL-316,243 in cell culture is orders of magnitude higher than the ~0.1 &#181;M dose required to achieve a maximal response33. Forskolin bypasses the adrenergic receptor, directly activating adenylyl cyclase and downstream lipolytic signaling. There are many more activators, as well as suppressors of lipolysis. When selecting a compound to stimulate lipolysis, the receptor-specificity and downstream signaling pathways should be carefully considered within the experimental design.
The rate of lipolysis in white adipose tissue is an important metabolic factor impacting cold tolerance and nutrient availability during fasting or exercise43,44,45,46. The purpose of this protocol is to measure the rate of lipolysis in adipocytes and adipose tissue, which will facilitate the understanding of adipocyte metabolism and how it may impact the metabolic phenotype of various murine models. To quantify the lipolytic rate, we measure the appearance of lipolytic products in the media (i.e., FFAs and glycerol). The method relies on the release of lipolytic products from the adipocyte into the media. Since white adipocytes express low levels of glycerol kinase, glycerol reuptake rates are low47. Conversely, the production of FFAs and glycerol by metabolic pathways other than lipolysis should also be considered. Adipocytes appear to express a phosphatase with activity against glycerol-3 phosphate, enabling the production of glycerol from glycerol-3-phosphate derived from glucose48,49,50. Glycolysis is a source of glycerol-3-phosphate used for FFA re-esterification in white adipocytes. When glucose levels are limited, glyceroneogenesis requires other 3-carbon sources, such as lactate and pyruvate51. The channeling of FFAs released by lipolysis within the cell and their metabolic fate is poorly understood; FFAs released by lipolysis must be converted to fatty acyl-CoA, before being re-esterified or undergoing &#946;-oxidation. It appears that FFAs released by lipolysis likely exit the cell before being taken back up and converted to fatty acyl-CoA52,53,54,55,56,57,58,59,60,61,62. FFAs can be sequestered outside of the cell by albumin. Importantly, long-chain FFAs are known to feedback-inhibit lipolysis if they are not sequestered by albumin63,64,65,66,67. Thus, optimizing the FFA buffering capacity of the media during the lipolysis assay is critical. The procedure described here is similar to previously published methods to measure the lipolytic rate in adipocytes and ex vivo adipose tissue from mice and humans15,68,69,70,71. This protocol differs through the use of serial sampling; by performing serial sampling, we can internally validate that lipolysis is being measured in the linear phase and utilize multiple measurements to calculate the rate of lipolysis, thereby reducing measurement error to increase confidence in the final calculated value. The drawback of serial sampling is that the assay requires more time and reagents; however, the longer timeframe reduces impact of measurement error on the standard error of the estimates of the rate. Additionally, this protocol measures both FFA and glycerol release, and considers the ratio of FFA:glycerol release with the goal of achieving a 3:1 ratio, as would be expected from complete lipolysis and release of lipolytic products into the media72.

<table><tbody><tr><td>24-Well tissue culture treated plate</td><td>Corning Inc</td><td>3527</td><td>Must be tissue culture treated for adipocyte differntiation</td></tr><tr><td>48-Well flat bottom plate with lid</td><td>Corning Inc</td><td>353078</td><td>Can be tissue culture treated</td></tr><tr><td>6-Well flat bottom plate with lid</td><td>Corning Inc</td><td>353046</td><td>Can be tissue culture treated</td></tr><tr><td>96-Well PCR Plate</td><td>USA sceintific</td><td>1402-9100</td><td>Any conical 0.2 mL PCR plate will be convenient&amp;nbsp;</td></tr><tr><td>Bovine Serum Albumin</td><td>Sigma Aldrich</td><td>A9418</td><td>FFA free BSA such as A8806, is also commonly used. The BSA should not have detectable FFA, also lot to lot variations in BSA can impact the observed rate of lipolysis</td></tr><tr><td>CL-316,243</td><td>Sigma Aldrich</td><td>C5976</td><td>CAS #: 138908-40-4 availaible from other suppliers</td></tr><tr><td>CO2 incubator</td><td>PHCBI</td><td>MCO-170AICUVH</td><td>CO2 should ideally be set to 10% for adipose tissue, however 5% CO2 will also work</td></tr><tr><td>DMEM, low glucose, no phenol red</td><td>Thermofischer</td><td>11054020</td><td>Any phenol red free media should work, DMEM/F12, RPMI, but should contain volatile buffering capacity, i.e. biocarbonate</td></tr><tr><td>FFA-free Bovine serum albumin</td><td>Equitech-Bio, Inc,&amp;nbsp;</td><td>BAH66</td><td></td></tr><tr><td>Free Glycerol Reagent</td><td>Sigma Aldrich</td><td>F6428</td><td></td></tr><tr><td>Glycerol Standard Solution</td><td>Sigma Aldrich</td><td>G7793&amp;nbsp;</td><td>This can also be made by diluting glycerol to the desired concentration</td></tr><tr><td>HR Series NEFA Standard Solution</td><td>Fujifilm</td><td>276-76491</td><td></td></tr><tr><td>HR Series NEFA-HR (2) Color Reagent A</td><td>Fujifilm</td><td>999-34691</td><td></td></tr><tr><td>HR Series NEFA-HR (2) Color Reagent B</td><td>Fujifilm</td><td>991-34891</td><td></td></tr><tr><td>HR Series NEFA-HR (2) Solvent A&amp;nbsp;</td><td>Fujifilm</td><td>995-34791</td><td></td></tr><tr><td>HR Series NEFA-HR (2) Solvent B&amp;nbsp;</td><td>Fujifilm</td><td>993-35191</td><td></td></tr><tr><td>Microbiological Incubator</td><td>Fischer Scientific</td><td>S28668</td><td>Any incubator at 37C can be used</td></tr><tr><td>Nunc MicroWell 96-Well Plates</td><td>Thermo Scientific</td><td>269620</td><td>Any optically clear, flat bottom 96-well plate works</td></tr><tr><td>Silicone Laboratory Benchtop Mat</td><td>VWR</td><td>76045-300</td><td>Glass plate can also be used. Absorbant surfaces are not recommended</td></tr><tr><td>Spectrophotometer/Microplate Reader</td><td>Molecular devices</td><td>SpectraMax i3x&amp;nbsp;</td><td>Any plate reader that can read at 540, 550 and 660 mm will work</td></tr><tr><td>V Bovine serum albumin</td><td>Sigma-Aldrich</td><td>810531</td><td></td></tr><tr><td>WypAll X70 Wipers</td><td>Kimberly-Clark</td><td>41200</td><td>Any high quality paper towel will work</td></tr></tbody></table>

measuring the rate of lipolysis in ex vivo murine adipose tissue and primary preadipocytes differentiated in vitro

Adipocytes store energy in the form of triglycerides in lipid droplets. This energy can be mobilized via lipolysis, where the fatty acid side chains are sequentially cleaved from the glycerol backbone, resulting in the release of free fatty acids and glycerol. Due to the low expression of glycerol kinase in white adipocytes, glycerol re-uptake rates are negligible, while fatty acid re-uptake is dictated by the fatty acid binding capacity of media components such as albumin. Both glycerol and fatty acid release into media can be quantified by colorimetric assays to determine the lipolytic rate. By measuring these factors at multiple time points, one can determine the linear rate of lipolysis with high confidence. Here, we provide a detailed protocol for the measurement of lipolysis in in vitro differentiated adipocytes and ex vivo adipose tissue from mice. This protocol may also be optimized for other preadipocyte cell lines or adipose tissue from other organisms; considerations and optimization parameters are discussed. This protocol is designed to be useful in determining and comparing the rate of adipocyte lipolysis between mouse models and treatments.

We measured the basal and stimulated lipolytic rate of in vitro differentiated adipocytes. Primary preadipocytes from inguinal white adipose tissue were differentiated into adipocytes by the treatment of confluent cells with 5 &#181;M dexamethasone, 0.5 mM IBMX, 1 &#181;g/mL insulin, and 1 &#181;M troglitazone for 4 days, followed by an additional 3 day treatment with 1 &#181;g/mL insulin. Cells were incubated in media without insulin for 24 h prior to the lipolysis assay. At time = 0h, the cells were washed onc...

Watch this Scientific Journal Video about Measuring the Rate of Lipolysis in Ex Vivo Murine Adipose Tissue and Primary Preadipocytes Differentiated In Vitro at JoVE.com

Measuring the Rate of Lipolysis in Ex Vivo Murine Adipose Tissue and Primary Preadipocytes Differentiated In Vitro

Triglyceride lipolysis in adipocytes is an important metabolic process resulting in the liberation of free fatty acids and glycerol. Here, we provide a detailed protocol to measure basal and stimulated lipolysis in adipocytes and ex vivo adipose tissue from mice.

Measuring the Rate of Lipolysis in Ex Vivo Murine Adipose Tissue and Primary Preadipocytes Differentiated In Vitro

Adipocytes store energy in the form of triglycerides in lipid droplets. This energy can be mobilized via lipolysis, where the fatty acid side chains are ...

measuring-rate-lipolysis-ex-vivo-murine-adipose-tissue-primary

Research

JoVE Journal

Biology

2.6K Views.  Weill Cornell Medicine. Triglyceride lipolysis in adipocytes is an important metabolic process resulting in the liberation of free fatty acids and glycerol. Here, we provide a detailed protocol to measure basal and stimulated lipolysis in adipocytes and ex vivo adipose tissue from mice.

Video: Measuring the Rate of Lipolysis in Ex Vivo Murine Adipose Tissue and Primary Preadipocytes Differentiated In Vitro

Measurement of Basal and Forskolin-stimulated Lipolysis in Inguinal Adipose Fat Pads

Lipolysis is a process by which the lipid stored as triglycerides in adipose tissues are hydrolyzed into glycerol and fatty acids. This article describes the method for the measurement of basal and forskolin (FSK)-stimulated lipolysis in the inguinal fat pads isolated from wild type mice fed either normal chow diet (NCD), high fat diet (HFD) or a high fat diet containing 0.01% of capsaicin (CAP; transient receptor potential vanilloid subfamily 1 (TRPV1) agonist) for 32 weeks. The method described here for performing ex vivo lipolysis is adopted from Schweiger et al.1 We present a detailed protocol for measuring glycerol levels by UV-Visible (UV/VIS) spectrophotometry. The method described here can be used to successfully isolate inguinal fat pads for lipolysis measurements to obtain consistent results. The protocol described for inguinal fat pads can readily be extended to measure lipolysis in other tissues.

This protocol describes the method of determining basal and forskolin-stimulated lipolysis in inguinal fat pads obtained from normal chow diet (NCD) or high fat diet (HFD) &plusmn; capsaicin fed wild type mice. As an index for lipolysis, glycerol release was measured from inguinal adipose fat pads.

Lipolysis is a process by which the lipid stored as triglycerides in adipose tissues are hydrolyzed into glycerol and fatty acids. This article describes ...

Biochemistry

Mechanism of Regulation of Adipocyte Numbers in Adult Organisms Through Differentiation and Apoptosis Homeostasis

Considering that adipose tissue (AT) is an endocrine organ, it can influence whole body metabolism. Excessive energy storage leads to the dysregulation of adipocytes, which in turn induces abnormal secretion of adipokines, triggering metabolic syndromes such as obesity, dyslipidemia, hyperglycemia, hyperinsulinemia, insulin resistance and type 2 diabetes. Therefore, investigating the molecular mechanisms behind adipocyte dysregulation could help to develop novel therapeutic strategies. Our protocol describes methods for evaluating the molecular mechanism affected by hypoxic conditions of the AT, which correlates with adipocyte apoptosis in adult mice. This protocol describes how to analyze AT in vivo through gene expression profiling as well as histological analysis of adipocyte differentiation, proliferation and apoptosis during hypoxia exposure, ascertained through staining of hypoxic cells or HIF-1&#945; protein. Furthermore, in vitro analysis of adipocyte differentiation and its responses to various stimuli completes the characterization of the molecular pathways behind possible adipocyte dysfunction leading to metabolic syndromes.

Adipose tissue (AT) can influence whole body homeostasis, therefore understanding the molecular mechanisms of adipocyte differentiation and function is of importance. We provide a protocol for gaining new insights into these processes by analyzing adipocyte homeostasis, differentiation and hypoxia exposure as a model for induced adipocyte apoptosis.

Considering that adipose tissue (AT) is an endocrine organ, it can influence whole body metabolism. Excessive energy storage leads to the dysregulation of ...

Developmental Biology

Localization, Identification, and Excision of Murine Adipose Depots

Obesity has increased dramatically in the last few decades and affects over one third of the adult US population. The economic effect of obesity in 2005 reached a staggering sum of $190.2 billion in direct medical costs alone. Obesity is a major risk factor for a wide host of diseases. Historically, little was known regarding adipose and its major and essential functions in the body. Brown and white adipose are the two main types of adipose but current literature has identified a new type of fat called brite or beige adipose. Research has shown that adipose depots have specific metabolic profiles and certain depots allow for a propensity for obesity and other related disorders. The goal of this protocol is to provide researchers the capacity to identify and excise adipose depots that will allow for the analysis of different factorial effects on adipose; as well as the beneficial or detrimental role adipose plays in disease and overall health. Isolation and excision of adipose depots allows investigators to look at gross morphological changes as well as histological changes. The adipose isolated can also be used for molecular studies to evaluate transcriptional and translational change or for in vitro experimentation to discover targets of interest and mechanisms of action. This technique is superior to other published techniques due to the design allowing for isolation of multiple depots with simplicity and minimal contamination.

Due to the drastic and negative connection between obesity and other comorbidities, research on the role adipose plays in disease and overall health is warranted. We present a protocol for the isolation and excision of adipose depots allowing for the study of adipose using in situ and in vitro methods.

Obesity has increased dramatically in the last few decades and affects over one third of the adult US population. The economic effect of obesity in 2005 ...

Medicine

Assessing Whole-Body Lipid-Handling Capacity in Mice

Assessing lipid metabolism is a cornerstone of evaluating metabolic function, and it is considered essential for in vivo metabolism studies. Lipids are a class of many different molecules with many pathways involved in their synthesis and metabolism. A starting point for evaluating lipid hemostasis for nutrition and obesity research is needed. This paper describes three easy and accessible methods that require little expertise or practice to master, and that can be adapted by most labs to screen for lipid-metabolism abnormalities in mice. These methods are (1) measuring several fasting serum lipid molecules using commercial kits (2) assaying for dietary lipid-handling capability through an oral intralipid tolerance test, and (3) evaluating the response to a pharmaceutical compound, CL 316,243, in mice. Together, these methods will provide a high-level overview of lipid handling capability in mice.

This paper provides three easy and accessible assays for assessing lipid metabolism in mice.

Assessing lipid metabolism is a cornerstone of evaluating metabolic function, and it is considered essential for in vivo metabolism studies. Lipids are a ...

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 oxidation, or alternatively, synthesize new lipid via de novo lipogenesis. The net sum of these pathways is dictated by a number of factors, which in certain disease states leads to fatty liver disease. Excess hepatic lipid accumulation is associated with whole body insulin resistance and coronary heart disease. Tools to study lipid metabolism in hepatocytes are useful to understand the role of hepatic lipid metabolism in certain metabolic disorders.
In the liver, hepatocytes regulate the breakdown and synthesis of fatty acids via &#946;-fatty oxidation and de novo lipogenesis, respectively. Quantifying metabolism in these pathways provides insight into hepatic lipid handling. Unlike in vitro quantification, using primary hepatocytes, making measurements in vivo is technically challenging and resource intensive. Hence, quantifying &#946;-fatty acid oxidation and de novo lipogenesis in cultured mouse hepatocytes provides a straight forward method to assess hepatocyte lipid handling. 
Here we describe a method for the isolation of primary mouse hepatocytes, and we demonstrate quantification of &#946;-fatty acid oxidation and de novo lipogenesis, using radiolabeled substrates.

De novo lipogenesis and &#946;-fatty acid oxidation constitute key metabolic pathways in hepatocyte, pathways that are perturbed in several metabolic disorders, including fatty liver disease. Here we demonstrate isolation of mouse primary hepatocytes and describe quantification of &#946;-fatty acid oxidation and lipogenesis.

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

Human SATMVECs: Isolation and Adipocyte Cross-Talk Studies

Studying Adipose Endothelial Cell/Adipocyte Cross-Talk in Human Subcutaneous Adipose Tissue

Microvascular endothelial cells (MVECs) have many critical roles, including control of vascular tone, regulation of thrombosis, and angiogenesis. Significant heterogeneity in endothelial cell (EC) genotype and phenotype depends on their vascular bed and host disease state. The ability to isolate MVECs from tissue-specific vascular beds and individual patient groups offers the opportunity to directly compare MVEC function in different disease states. Here, using subcutaneous adipose tissue (SAT) taken at the time of insertion of cardiac implantable electronic devices (CIED), we describe a method for the isolation of a pure population of functional human subcutaneous adipose tissue MVEC (hSATMVEC) and an experimental model of hSATMVEC-adipocyte cross-talk.
hSATMVEC were isolated following enzymatic digestion of SAT by incubation with anti-CD31 antibody-coated magnetic beads and passage through magnetic columns. hSATMVEC were grown and passaged on gelatin-coated plates. Experiments used cells at passages 2-4. Cells maintained classic features of EC morphology until at least passage 5. Flow cytometric assessment showed 99.5% purity of isolated hSATMVEC, defined as CD31+/CD144+/CD45-. Isolated hSATMVEC from controls had a population doubling time of approximately 57 h, and active proliferation was confirmed using a cell proliferation imaging kit. Isolated hSATMVEC function was assessed using their response to insulin stimulation and angiogenic tube-forming potential. We then established an hSATMVEC-subcutaneous adipocyte co-culture model to study cellular cross-talk and demonstrated a downstream effect of hSATMVEC on adipocyte function.
hSATMVEC can be isolated from SAT taken at the time of CIED insertion and are of sufficient purity to both experimentally phenotype and study hSATMVEC-adipocyte cross-talk.

Author Spotlight: Insights into Cardiometabolic Diseases with Subcutaneous Adipose Tissue Microvasculature Studies 

Here, we describe a protocol for isolating, culturing, and phenotyping microvascular endothelial cells from human subcutaneous adipose tissue (hSATMVECs). Additionally, we describe an experimental model of hSATMVEC-adipocyte cross-talk.

Microvascular endothelial cells (MVECs) have many critical roles, including control of vascular tone, regulation of thrombosis, and angiogenesis. ...

Isolation and Differentiation of Primary White and Brown Preadipocytes from Newborn Mice

The understanding of the mechanisms underlying adipocyte differentiation and function has greatly benefited from the use of immortalized white preadipocyte cell lines. These cultured cell lines, however, have limitations. They do not fully capture the diverse functional spectrum of the heterogenous adipocyte populations that are now known to exist within white adipose depots. To provide a more physiologically relevant model to study the complexity of white adipose tissue, a protocol has been developed and optimized to enable simultaneous isolation of primary white and brown adipocyte progenitors from newborn mice, their rapid expansion in culture, and their differentiation in vitro into mature, fully functional adipocytes. The primary advantage of isolating primary cells from newborn, rather than adult mice, is that the adipose depots are actively developing and are, therefore, a rich source of proliferating preadipocytes. Primary preadipocytes isolated using this protocol differentiate rapidly upon reaching confluence and become fully mature in 4-5 days, a temporal window that accurately reflects the appearance of developed fat pads in newborn mice. Primary cultures prepared using this strategy can be expanded and studied with high reproducibility, making them suitable for genetic and phenotypic screens and enabling the study of the cell-autonomous adipocyte phenotypes of genetic mouse models. This protocol offers a simple, rapid, and inexpensive approach to study the complexity of adipose tissue in vitro.

This report describes a protocol for the simultaneous isolation of primary brown and white preadipocytes from newborn mice. Isolated cells can be grown in culture and induced to differentiate into fully mature white and brown adipocytes. The method enables genetic, molecular, and functional characterization of primary fat cells in culture.

The understanding of the mechanisms underlying adipocyte differentiation and function has greatly benefited from the use of immortalized white ...

Differentiated Mouse Adipocytes in Primary Culture: A Model of Insulin Resistance

Insulin resistance is a reduced effect of insulin on its target cells, usually derived from decreased insulin receptor signaling. Insulin resistance contributes to the development of type 2 diabetes (T2D) and other obesity-derived diseases of high prevalence worldwide. Therefore, understanding the mechanisms underlying insulin resistance is of great relevance. Several models have been used to study insulin resistance both in vivo and in vitro; primary adipocytes represent an attractive option to study the mechanisms of insulin resistance and identify molecules that counteract this condition and the molecular targets of insulin-sensitizing drugs. Here, we have established an insulin resistance model using primary adipocytes in culture treated with tumor necrosis factor-&#945; (TNF-&#945;).
Adipocyte precursor cells (APCs), isolated from collagenase-digested mouse subcutaneous adipose tissue by magnetic cell separation technology, are differentiated into primary adipocytes. Insulin resistance is then induced by treatment with TNF-&#945;, a proinflammatory cytokine that reduces the tyrosine phosphorylation/activation of members of the insulin signaling cascade. Decreased phosphorylation of insulin receptor (IR), insulin receptor substrate (IRS-1), and protein kinase B (AKT) are quantified by western blot. This method provides an excellent tool to study the mechanisms mediating insulin resistance in adipose tissue.

This protocol describes the isolation of mouse preadipocytes from subcutaneous fat, their differentiation into mature adipocytes, and the induction of insulin resistance. Insulin action is evaluated by the phosphorylation/activation of members of the insulin signaling pathway through western blot. This method allows direct determination of insulin resistance/sensitivity in primary adipocytes.

Insulin resistance is a reduced effect of insulin on its target cells, usually derived from decreased insulin receptor signaling. Insulin resistance ...

Semi-Automated Isolation of Murine White Adipose Tissue

Semi-Automated Isolation of the Stromal Vascular Fraction from Murine White Adipose Tissue Using a Tissue Dissociator

The in vitro study of white, brown, and beige adipocyte differentiation enables the investigation of cell-autonomous functions of adipocytes and their mechanisms. Immortalized white preadipocyte cell lines are publicly available and widely used. However, the emergence of beige adipocytes in white adipose tissue in response to external cues is difficult to recapitulate to the full extent using publicly available white adipocyte cell lines. Isolation of the stromal vascular fraction (SVF) from murine adipose tissue is commonly executed to obtain primary preadipocytes and perform adipocyte differentiation. However, mincing and collagenase digestion of adipose tissue by hand can result in experimental variation and is prone to contamination. Here, we present a modified semi-automated protocol that utilizes a tissue dissociator for collagenase digestion to achieve easier isolation of the SVF, with the aim of reducing experimental variation, reducing contamination, and increasing reproducibility. The obtained preadipocytes and differentiated adipocytes can be used for functional and mechanistic analyses.

Author Spotlight: Semi-Automated Isolation of the Stromal Vascular Fraction from Murine White Adipose Tissue Using a Tissue Dissociator  

This protocol describes the semi-automated isolation of the stromal vascular fraction (SVF) from murine adipose tissue to obtain preadipocytes and achieve adipocyte differentiation in vitro. Using a tissue dissociator for collagenase digestion reduces experimental variation and increases reproducibility.

The in vitro study of white, brown, and beige adipocyte differentiation enables the investigation of cell-autonomous functions of adipocytes and their ...

Measuring In Vivo Adipose Tissue Kinetics in Humans Using the Deuterium (2H)-Labeling Approach

White adipose tissue is a highly plastic organ that is necessary to maintain whole-body energy homeostasis. The adipose tissue mass and changes in the fat mass or distribution are regulated by changes in the synthesis and breakdown (i.e., turnover) of adipose cells and triacylglycerols. Evidence suggests that the manner and magnitude of subcutaneous adipose tissue expansion (i.e., hypertrophy vs. hyperplasia) and turnover can influence metabolic health, as adipogenesis has been implicated in the pathogenesis of obesity and related diseases. Despite the potential role of adipose turnover in human health, there is a lack of knowledge about the in vivo kinetics of adipose cells. This is due, in part, to the slow turnover rate of the cells in adipose tissue and the practical complexity of directly labeling their metabolic precursors in vivo. Herein, we describe methods to measure in vivo adipose kinetics and turnover rates in humans through the consumption of deuterium (2H)-labeled water. The incorporation of 2H into the deoxyribonucleotide moieties of DNA in pre-adipocytes and adipocytes provides an accurate measure of cell formation and death (adipose turnover). Overall, this is an innovative approach to measuring in vivo adipose kinetics and represents a substantive departure from other in vitro assessments.

Measuring In Vivo Adipose Tissue Kinetics in Humans Using the Deuterium 2H-Labeling Approach

Presented here is a protocol to measure in vivo adipose tissue kinetics in humans using the deuterium (2H)-labeling method.

White adipose tissue is a highly plastic organ that is necessary to maintain whole-body energy homeostasis. The adipose tissue mass and changes in the fat ...

Measuring the Rate of Lipolysis in Ex Vivo Murine Adipose Tissue and Primary Preadipocytes Differentiated In Vitro

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Measurement of Basal and Forskolin-stimulated Lipolysis in Inguinal Adipose Fat Pads

Mechanism of Regulation of Adipocyte Numbers in Adult Organisms Through Differentiation and Apoptosis Homeostasis

Localization, Identification, and Excision of Murine Adipose Depots

Assessing Whole-Body Lipid-Handling Capacity in Mice

Determination of Fatty Acid Oxidation and Lipogenesis in Mouse Primary Hepatocytes

Studying Adipose Endothelial Cell/Adipocyte Cross-Talk in Human Subcutaneous Adipose Tissue

Isolation and Differentiation of Primary White and Brown Preadipocytes from Newborn Mice

Differentiated Mouse Adipocytes in Primary Culture: A Model of Insulin Resistance

Semi-Automated Isolation of the Stromal Vascular Fraction from Murine White Adipose Tissue Using a Tissue Dissociator

Measuring In Vivo Adipose Tissue Kinetics in Humans Using the Deuterium (²H)-Labeling Approach