The authors wish to acknowledge support from Dr. Lavoisier Ramos-Espiritu at the Rockefeller High Throughput and Spectroscopy Resource Center.

Sperm are collected from 8-16-week-old CD-1 male mice. Animal experiments were approved by Weill Cornell Medicine&#39;s Institutional Animal Care and Use Committee (IACUC).
1. Day prior to assay
<ol>
	<li>Preparation of sensor cartridge and extracellular flux analyzer calibrant
	<ol>
		<li>To hydrate the sensor cartridge, remove the sensor cartridge from the XFe96 Extracellular Flux Assay Kit and place the sensor cartridge upside down next to the utility plate.</li>
		<li>Fi...

<ol>
	<li>Wu, M., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Multiparameter+metabolic+analysis+reveals+a+close+link+between+attenuated+mitochondrial+bioenergetic+function+and+enhanced+glycolysis+dependency+in+human+tumor+cells.">Multiparameter metabolic analysis reveals a close link between attenuated mitochondrial bioenergetic function and enhanced glycolysis dependency in human tumor cells.</a> American Journal of Physiology - Cell Physiology. 292 (1), C125-C136 (2007).</li><li>Amo, T., Yadava, N., Oh, R., Nicholls, D. G., Brand, M. D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Experimental+assessment+of+bioenergetic+differences+caused+by+the+common+European+mitochondrial+DNA+haplogroups+H+and+T.">Experimental assessment of bioenergetic differences caused by the common European mitochondrial DNA haplogroups H and T.</a> Gene. 411 (1-2), 69-76 (2008).</li><li>Choi, S. W., Gerencser, A. A., Nicholls, D. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Bioenergetic+analysis+of+isolated+cerebrocortical+nerve+terminals+on+a+microgram+scale:+spare+respiratory+capacity+and+stochastic+mitochondrial+failure.">Bioenergetic analysis of isolated cerebrocortical nerve terminals on a microgram scale: spare respiratory capacity and stochastic mitochondrial failure.</a> Journal of Neurochemistry. 109 (4), 1179-1191 (2009).</li><li>de Groof, A. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Increased+OXPHOS+activity+precedes+rise+in+glycolytic+rate+in+H-RasV12/E1A+transformed+fibroblasts+that+develop+a+Warburg+phenotype.">Increased OXPHOS activity precedes rise in glycolytic rate in H-RasV12/E1A transformed fibroblasts that develop a Warburg phenotype.</a> Molecular Cancer. 8, 54 (2009).</li><li>Chao, L. C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Insulin+resistance+and+altered+systemic+glucose+metabolism+in+mice+lacking+Nur77.">Insulin resistance and altered systemic glucose metabolism in mice lacking Nur77.</a> Diabetes. 58 (12), 2788-2796 (2009).</li><li>Chang, M. C. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Fertilizing+capacity+of+spermatozoa+deposited+into+the+fallopian+tubes.">Fertilizing capacity of spermatozoa deposited into the fallopian tubes.</a> Nature. 168 (4277), 697-698 (1951).</li><li>Austin, C. R., Bishop, M. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Role+of+the+rodent+acrosome+and+perforatorium+in+fertilization.">Role of the rodent acrosome and perforatorium in fertilization.</a> Proceedings of the Royal Society of London. Series B, Biological Sciences. 149 (935), 241-248 (1958).</li><li>Ishijima, S., Baba, S. A., Mohri, H., Suarez, S. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Quantitative+analysis+of+flagellar+movement+in+hyperactivated+and+acrosome-reacted+golden+hamster+spermatozoa.">Quantitative analysis of flagellar movement in hyperactivated and acrosome-reacted golden hamster spermatozoa.</a> Molecular Reproduction and Development. 61 (3), 376-384 (2002).</li><li>Suarez, S. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Control+of+hyperactivation+in+sperm.">Control of hyperactivation in sperm.</a> Human Reproduction Update. 14 (6), 647-657 (2008).</li><li>Goodson, S. G., Qiu, Y., Sutton, K. A., Xie, G., Jia, W., O'Brien, D. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Metabolic+substrates+exhibit+differential+effects+on+functional+parameters+of+mouse+sperm+capacitation.">Metabolic substrates exhibit differential effects on functional parameters of mouse sperm capacitation.</a> Biology of Reproduction. 87 (3), 75 (2012).</li><li>Travis, A. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Functional+relationships+between+capacitation-dependent+cell+signaling+and+compartmentalized+metabolic+pathways+in+murine+spermatozoa.">Functional relationships between capacitation-dependent cell signaling and compartmentalized metabolic pathways in murine spermatozoa.</a> Journal of Biological Chemistry. 276 (10), 7630-7636 (2001).</li><li>Urner, F., Leppens-Luisier, G., Sakkas, D. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Protein+tyrosine+phosphorylation+in+sperm+during+gamete+interaction+in+the+mouse:+the+influence+of+glucose.">Protein tyrosine phosphorylation in sperm during gamete interaction in the mouse: the influence of glucose.</a> Biology of Reproduction. 64 (5), 1350-1357 (2001).</li><li>Danshina, P. V., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Phosphoglycerate+kinase+2+(PGK2)+is+essential+for+sperm+function+and+male+fertility+in+mice.">Phosphoglycerate kinase 2 (PGK2) is essential for sperm function and male fertility in mice.</a> Biology of Reproduction. 82 (1), 136-145 (2010).</li><li>Miki, K., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Glyceraldehyde+3-phosphate+dehydrogenase-S,+a+sperm-specific+glycolytic+enzyme,+is+required+for+sperm+motility+and+male+fertility.">Glyceraldehyde 3-phosphate dehydrogenase-S, a sperm-specific glycolytic enzyme, is required for sperm motility and male fertility.</a> Proceedings of the National Academy of Sciences. 101 (47), 16501-16506 (2004).</li><li>Mori, C., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mouse+spermatogenic+cell-specific+type+1+hexokinase+(mHk1-s)+transcripts+are+expressed+by+alternative+splicing+from+the+mHk1+gene+and+the+HK1-S+protein+is+localized+mainly+in+the+sperm+tail.">Mouse spermatogenic cell-specific type 1 hexokinase (mHk1-s) transcripts are expressed by alternative splicing from the mHk1 gene and the HK1-S protein is localized mainly in the sperm tail.</a> Molecular Reproduction and Development. 49 (4), 374-385 (1998).</li><li>Westhoff, D., Kamp, G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Glyceraldehyde+3-phosphate+dehydrogenase+is+bound+to+the+fibrous+sheath+of+mammalian+spermatozoa.">Glyceraldehyde 3-phosphate dehydrogenase is bound to the fibrous sheath of mammalian spermatozoa.</a> Journal of Cell Science. 110 (15), 1821-1829 (1997).</li><li>Nevo, A. C., Rikmenspoel, R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Diffusion+of+ATP+in+sperm+flagella.">Diffusion of ATP in sperm flagella.</a> Journal of Theoretical Biology. 26 (1), 11-18 (1970).</li><li>Adam, D. E., Wei, J. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Mass+transport+of+ATP+within+the+motile+sperm.">Mass transport of ATP within the motile sperm.</a> Journal of Theoretical Biology. 49 (1), 125-145 (1975).</li><li>Tombes, R. M., Shapiro, B. M. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Enzyme+termini+of+a+phosphocreatine+shuttle.+Purification+and+characterization+of+two+creatine+kinase+isozymes+from+sea+urchin+sperm.">Enzyme termini of a phosphocreatine shuttle. Purification and characterization of two creatine kinase isozymes from sea urchin sperm.</a> Journal of Biological Chemistry. 262 (33), 16011-16019 (1987).</li><li>Gomendio, M., Tourmente, M., Roldan, E. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Why+mammalian+lineages+respond+differently+to+sexual+selection:+metabolic+rate+constrains+the+evolution+of+sperm+size.">Why mammalian lineages respond differently to sexual selection: metabolic rate constrains the evolution of sperm size.</a> Proceedings of the Royal Society of Biological Sciences. 278 (1721), 3135-3141 (2011).</li><li>Tourmente, M., Villar-Moya, P., Rial, E., Roldan, E. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Differences+in+ATP+generation+via+glycolysis+and+oxidative+phosphorylation+and+relationships+with+sperm+motility+in+mouse+species.">Differences in ATP generation via glycolysis and oxidative phosphorylation and relationships with sperm motility in mouse species.</a> Journal of Biological Chemistry. 290 (33), 20613-20626 (2015).</li><li>Visconti, P. E., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Capacitation+of+mouse+spermatozoa.+II.+Protein+tyrosine+phosphorylation+and+capacitation+are+regulated+by+a+cAMP-dependent+pathway.">Capacitation of mouse spermatozoa. II. Protein tyrosine phosphorylation and capacitation are regulated by a cAMP-dependent pathway.</a> Development. 121 (4), 1139-1150 (1995).</li><li>Buck, J., Sinclair, M. L., Schapal, L., Cann, M. J., Levin, L. R. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Cytosolic+adenylyl+cyclase+defines+a+unique+signaling+molecule+in+mammals.">Cytosolic adenylyl cyclase defines a unique signaling molecule in mammals.</a> PNAS. 96 (1), 79-84 (1999).</li><li>Visconti, P. E., Bailey, J. L., Moore, G. D., Pan, D., Olds-Clarke, P., Kopf, G. S. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Capacitation+of+mouse+spermatozoa.+I.+Correlation+between+the+capacitation+state+and+protein+tyrosine+phosphorylation.">Capacitation of mouse spermatozoa. I. Correlation between the capacitation state and protein tyrosine phosphorylation.</a> Development. 121 (4), 1129-1137 (1995).</li><li>Morgan, D. J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Tissue-specific+PKA+inhibition+using+a+chemical+genetic+approach+and+its+application+to+studies+on+sperm+capacitation.">Tissue-specific PKA inhibition using a chemical genetic approach and its application to studies on sperm capacitation.</a> PNAS. 105 (52), 20740-20745 (2008).</li><li>Lybaert, P., Danguy, A., Leleux, F., Meuris, S., Lebrun, P. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed&cmd=Search&doptcmdl=Citation&defaultField=Title+Word&term=Improved+methodology+for+the+detection+and+quantification+of+the+acrosome+reaction+in+mouse+spermatozoa.">Improved methodology for the detection and quantification of the acrosome reaction in mouse spermatozoa.</a> Histology and Histopathology. 24 (8), 999-1007 (2009).</li></ol>

The loss of sperm capacitation in the absence of certain metabolic substrates or critical metabolic enzymes revealed energy metabolism as a key factor supporting successful fertilization. A metabolic switch during cell activation is a well-established concept in other cell types, however, we are just beginning to understand how sperm adapt their metabolism to the increasing energy demand during capacitation. Using an extracellular flux analyzer, we developed an easily applicable tool to monitor changes in glycolysis and ...

The application of mass spectrometry has revolutionized the study of metabolism. Targeted metabolic profiling and metabolomic tracing allow precise monitoring of changes in energy metabolism. However, performing metabolomics successfully requires extensive training, experienced staff, and expensive, highly sensitive mass spectrometers not readily available to every laboratory. In recent years, using an extracellular flux analyzer, such as the Seahorse XFe96 has grown popular as a surrogate method for measuring changes in energy metabolism in various cell types1,2,3,4,5.
Sperm are highly specialized motile cells; whose task is to deliver the paternal genome to the oocyte. Sperm leaving the male reproductive tract after ejaculation are still functionally immature and cannot fertilize the oocyte because they are unable to penetrate the oocytes&#39; vestments. Sperm acquire fertilization competence as they transit through the female reproductive tract in a maturation process known as capacitation6,7. Freshly ejaculated sperm or sperm dissected from the cauda epididymis can be capacitated in vitro by incubation in defined capacitation media containing Ca2+, bicarbonate (HCO3-) or a cell-permeable cAMP analog (e.g., dibutyryl-cAMP), a cholesterol acceptor (e.g., bovine serum albumin, BSA), and an energy source (e.g., glucose). During capacitation, sperm modify their motility pattern into an asymmetric flagellar beat, representing a swimming mode called hyperactivation8,9, and they become competent to undergo the acrosome reaction7, where proteolytic enzymes are released that digest the oocytes&#39; vestments. These processes require energy, and similar to somatic cells, sperm generate ATP and other high energy compounds via glycolysis as well as mitochondrial TCA cycle and oxidative phosphorylation (oxphos)10. While multiple studies demonstrate that glycolysis is necessary and sufficient to support sperm capacitation11,12,13,14, the contribution of oxphos is less clear. Contrary to other cell types where glycolysis is physically coupled to the TCA cycle, sperm are highly compartmentalized and are thought to maintain these processes in separate flagellar compartments: the midpiece concentrates the mitochondrial machinery, whereas the key enzymes of glycolysis appear to be restricted to the principal piece15,16. This compartmentalization results in an ongoing debate about whether pyruvate produced in the principal piece by glycolysis can support mitochondrial oxphos in the midpiece, and whether ATP produced by oxphos in the midpiece would be able to diffuse sufficiently rapidly along the length of the flagellum to support the energy requirements in distal parts of the principal piece17,18,19. There is also support of a role for oxphos in sperm capacitation. Not only is oxphos more energetically favorable than glycolysis, generating 16 times more ATP than glycolysis, but midpiece volume and mitochondrial content are directly correlated with reproductive fitness in mammalian species which exhibit greater degrees of competition between males for mates20. Addressing these questions requires methods for examining the relative contributions of glycolysis and oxphos during sperm capacitation.
Tourmente et al. applied a 24-well extracellular flux analyzer to compare the energy metabolism of closely related mouse species with significantly different sperm performance parameters21. Instead of reporting the basal ECAR and OCR values of non-capacitated sperm, here, we adapt their method using a 96-well extracellular flux analyzer to monitor changes in energy metabolism during mouse sperm capacitation in real-time. We developed a method that allows simultaneously monitoring glycolysis and oxphos in real-time in sperm with beating flagella in up to twelve different experimental conditions by measuring the flux of oxygen (O2) and protons (H+) (Figure 1A). Due to the breakdown of pyruvate to lactate during glycolysis and the production of CO2 via the TCA-cycle, non-capacitated and capacitated sperm extrude H+ into the assay media which are detected by the extracellular flux analyzer via H+-sensitive fluorophores immobilized to the probe tip of a sensor cartridge. In parallel, O2 consumption by oxidative phosphorylation is detected via O2-sensitive fluorophores immobilized to the same probe tip (Figure 1B). Effective detection of the released H+ and consumed O2 requires a modified sperm buffer with low buffering capacity without bicarbonate or phenol red. Thus, to induce capacitation in the absence of bicarbonate, we adopted the use of a cell-permeable cAMP analog injected together with the broad-range PDE inhibitor IBMX22. Three additional independent injection ports allow the injection of pharmacological activators and/or inhibitors, which facilitates real-time detection of changes in cellular respiration and glycolysis rate due to experimental manipulation.

<table border="1" fo:keep-together.within-page="1" fo:keep-with-next.within-page="always">
	<tbody>
		<tr>
			<td>Reagents</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>2-Deoxy-D-glucose</td>
			<td>Sigma-Aldrich</td>
			<td>D8375</td>
			<td>2-DG</td>
		</tr>
		<tr>
			<td>3-Isobutyl-1-methylxanthine</td>
			<td>Sigma-Aldrich</td>
			<td>I7018</td>
			<td>IBMX; prepare a 500 mM stock solution in DMSO (111.1 mg/ml) and store in small aliquots</td>
		</tr>
		<tr>
			<td>Antimycin A</td>
			<td>Sigma-Aldrich</td>
			<td>A8674</td>
			<td>AntA; prepare a 5 mM stock solution in DMSO (2.7 mg/ml) and store in small aliquots</td>
		</tr>
		<tr>
			<td>Bovine serum albumin</td>
			<td>Sigma-Aldrich</td>
			<td>A1470</td>
			<td>BSA</td>
		</tr>
		<tr>
			<td>Calcium chloride</td>
			<td>Sigma-Aldrich</td>
			<td>C1016</td>
			<td>CaCl2</td>
		</tr>
		<tr>
			<td>Concanacalin A, Lectin from Arachis hypogaea (peanut)</td>
			<td>Sigma-Aldrich</td>
			<td>L7381</td>
			<td>ConA</td>
		</tr>
		<tr>
			<td>Glucose</td>
			<td>Sigma-Aldrich</td>
			<td>G7528</td>
			<td></td>
		</tr>
		<tr>
			<td>Hepes</td>
			<td>Sigma-Aldrich</td>
			<td>H0887</td>
			<td></td>
		</tr>
		<tr>
			<td>Isothesia</td>
			<td>Henry Schein Animal Health</td>
			<td>1169567761</td>
			<td>Isoflurane</td>
		</tr>
		<tr>
			<td>Magnesium sulfate</td>
			<td>Sigma-Aldrich</td>
			<td>M2643</td>
			<td>MgSO4</td>
		</tr>
		<tr>
			<td>N6,2&#39;-O-Dibutyryladenosine 3&#39;,5&#39;-cyclic monophosphate sodium salt</td>
			<td>Sigma-Aldrich</td>
			<td>D0627</td>
			<td>db-cAMP</td>
		</tr>
		<tr>
			<td>Potassium chloride</td>
			<td>Sigma-Aldrich</td>
			<td>P9333</td>
			<td>KCl</td>
		</tr>
		<tr>
			<td>Potassium dihydrogen phosphate</td>
			<td>Sigma-Aldrich</td>
			<td>P5655</td>
			<td>KH2PO4</td>
		</tr>
		<tr>
			<td>Rotenone</td>
			<td>Cayman Chemical Company</td>
			<td>13995</td>
			<td>Rot; prepare a 5 mM stock solution in DMSO (2mg/ml) and store in small aliquots</td>
		</tr>
		<tr>
			<td>Sodium bicarbonate</td>
			<td>Sigma-Aldrich</td>
			<td>S5761</td>
			<td>NaHCO3-</td>
		</tr>
		<tr>
			<td>Sodium chloride</td>
			<td>Sigma-Aldrich</td>
			<td>S9888</td>
			<td>NaCl</td>
		</tr>
		<tr>
			<td>Equipment and materials</td>
			<td></td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>12 channel pipette 10-100 &#956;L</td>
			<td>eppendorf</td>
			<td>ES-12-100</td>
			<td></td>
		</tr>
		<tr>
			<td>12 channel pipette 50-300 &#956;L</td>
			<td>vwr</td>
			<td>613-5257</td>
			<td></td>
		</tr>
		<tr>
			<td>37 &#176;C, non-CO2 incubator</td>
			<td>vwr</td>
			<td>1545</td>
			<td></td>
		</tr>
		<tr>
			<td>5 mL cetrifuge tubes</td>
			<td>eppendorf</td>
			<td>30119380</td>
			<td></td>
		</tr>
		<tr>
			<td>50 mL conical centrifuge tubes</td>
			<td>vwr</td>
			<td>76211-286</td>
			<td></td>
		</tr>
		<tr>
			<td>Centrifuge with plate adapter</td>
			<td>Thermo Scientific</td>
			<td>IEC FL40R</td>
			<td></td>
		</tr>
		<tr>
			<td>Dissection kit</td>
			<td>World Precision Instruments</td>
			<td>MOUSEKIT</td>
			<td></td>
		</tr>
		<tr>
			<td>Inverted phase contrast microscope with 40X objective</td>
			<td>Nikon</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>OctaPool Solution Reservoirs, 25 ml, divided</td>
			<td>Thomas Scientific</td>
			<td>1159X93</td>
			<td></td>
		</tr>
		<tr>
			<td>OctaPool Solution Reservoirs, 25 mL, divided</td>
			<td>Thomas Scientific</td>
			<td>1159X95</td>
			<td></td>
		</tr>
		<tr>
			<td>Seahorse XFe96 Analyzer</td>
			<td>Agilent</td>
			<td></td>
			<td></td>
		</tr>
		<tr>
			<td>Seahorse XFe96 FluxPak</td>
			<td>Agilent</td>
			<td>102416-100</td>
			<td>Also sold as XFe96 FluxPak mini (102601-100) with 6 instead of 18 cartidges.</td>
		</tr>
	</tbody>
</table>

using an extracellular flux analyzer to measure changes in glycolysis and oxidative phosphorylation during mouse sperm capacitation

Mammalian sperm acquire fertilization capacity in the female reproductive tract in a process known as capacitation. Capacitation-associated processes require energy. There remains an ongoing debate about the sources generating the ATP which fuels sperm progressive motility, capacitation, hyperactivation, and acrosome reaction. Here, we describe the application of an extracellular flux analyzer as a tool to analyze changes in energy metabolism during mouse sperm capacitation. Using H+- and O2- sensitive fluorophores, this method allows monitoring glycolysis and oxidative phosphorylation in real-time in non-capacitated versus capacitating sperm. Using this assay in the presence of different energy substrates and/or pharmacological activators and/or inhibitors can provide important insights into the contribution of different metabolic pathways and the intersection between signaling cascades and metabolism during sperm capacitation.

This method uses an extracellular flux analyzer to monitor real-time changes in the rate of glycolysis and oxphos during mouse sperm capacitation. Figure 4 shows an exemplary experiment where sperm were capacitated in the presence of glucose as the only energy substrate and 2-DG and antimycin and rotenone as pharmacological modulators. The energy substrate in the extracellular flux analyzer TYH buffer and the pharmacological modulators can be freely selected ...

Watch this Scientific Journal Video about Using an Extracellular Flux Analyzer to Measure Changes in Glycolysis and Oxidative Phosphorylation during Mouse Sperm Capacitation at JoVE.com

Using an Extracellular Flux Analyzer to Measure Changes in Glycolysis and Oxidative Phosphorylation during Mouse Sperm Capacitation

We describe the application of an extracellular flux analyzer to monitor real-time changes in glycolysis and oxidative phosphorylation during mouse sperm capacitation.

Mammalian sperm acquire fertilization capacity in the female reproductive tract in a process known as capacitation. Capacitation-associated processes ...

This protocol can be used to apply an extracellular flux analyzer to monitor changes in energy metabolism during sperm capacitation. We developed this protocol to compare changes in glycolysis and oxidative phosphorylation in real time between non-capacitated and capacitated mouse sperm. On the day before the assay, remove the sensor cartridge from an extracellular flux assay kit and place the cartridge upside down next to the utility plate.Fill a solution reservoir with 25 milliliters of double distilled water and add 200 microliters of water to each well of the utility plate, then place the sensor cartridge back into the utility plate. Place the plate into a 37 degree Celsius non-carbon dioxide incubator. Next, aliquot 25 milliliters of extracellular flux analyzer calibrant into a 50 milliliter conical tube and place the tube into the 37 degree Celsius non-carbon dioxide incubator.To prepare ConA coated micro plates, dissolve 2.5 milligrams of ConA in five milliliters of double distilled water and use a multichannel pipette to fill each well of an extracellular flux analyzer 96-well plate with 50 microliters of the ConA solution, then leave the lid open to let the plate dry overnight. To prepare the sperm buffer, heat 250 milliliters of extracellular flux analyzer TYH buffer to 37 degrees Celsius and adjust the pH to 7.4. On the day of the assay, replace the water in each well of the utility plate with 200 microliters of XF calibrant per well and place the plate back into the non-carbon dioxide incubator for at least one hour.To generate a wave template, turn on the extracellular flux analyzer. While the temperature is stabilizing to 37 degrees Celsius, open the wave software and open a blank template. Under the group definitions tab, define the assay medium as TYH and the cell type as mouse sperm, leaving the injection strategies and pretreatments blank.Create different groups for each assay condition and open the plate map to assign each group to specific wells. Under the protocol tab, unhighlight equilibrate, add each of four different measurement cycles, select the respective port, and edit the measurement details so that the measure after injection is highlighted, then save the assay template, fill out the project summary and save the results. Before harvesting the sperm, prewarm 50 milliliters of TYH buffer at 37 degrees Celsius.After harvesting caudas from adult male mice, place each cauda in 500 microliters of the pre-warmed TYH buffer in individual wells of a 24-well plate. Use forceps to immobilize each cauda individually at the bottom of each well and quickly make five to seven small incisions in each tissue using feather scissors. When all of the caudas have been incised, immediately place the plate into the non-carbon dioxide incubator to allow the sperm to disperse for 15 minutes.To load the sensor cartridge, remove the lid from the sensor cartridge and align the letter of the respective port loading guide with the upper left corner of the cartridge. Holding the port loading guide in place, insert the pipette tips vertically into the port loading guide holes of port A and inject 20 microliters of TYH buffer into every column. For port B, inject 22 microliters of TYH buffer into columns one through four, 22 microliters of 500 millimolar 2-deoxyglucose into columns five through eight, and 25 microliters of five micromolar antimycin A rotenone into columns nine through 12.For port C, inject 25 microliters of TYH buffer into every column with odd numbers and 25 microliters of 10 millimolar of dibutyryl-cyclic AMP 500 micromolar IBMX into every column with even numbers, then place the sensor cartridge with a calibration plate into the extracellular flux analyzer and start the assay. The calibration will take 10 to 15 minutes. To prepare the sperm plates, add three milliliters of three milligrams per milliliter bovine serum albumin in TYH buffer to each of three five milliliter centrifuge tubes.Next, pool two wells of sperm into each of three 1.5 milliliter centrifuge tubes. After counting, dilute the sperm to a two times 10 to the seven sperm per milliliter concentration per sample in fresh TYH supplemented with bovine serum albumin. Sediment the sperm by centrifugation and resuspend the sperm pellets in one milliliter of TYH buffer.Centrifuge the sperm again and remove the supernatants taking care not to disturb the pellets. Transfer each sperm suspension into one of the prepared five milliliter centrifuge tubes and add 180 microliters of TYH buffer into each corner well of a ConA coated plate. Add 180 microliters of sperm into each empty well of the ConA coated plate and centrifuge the plate two times rotating the plate 180 degrees between centrifugations, then place the calibration plate with the sperm plate and continue the assay.In this representative experiment, sperm were capacitated in the presence of glucose as the only energy substrate and 2-deoxyglucose and antimycin and rotenone as the pharmacological modulators. The arrow indicates induction of capacitation. In the presence of glucose, capacitation was accompanied by a seven-fold increase in the extracellular acidification rate which is inhibited by blocking glycolysis with 2-deoxyglucose.Capacitated sperm demonstrated a 20-fold increase in the oxygen consumption rate compared to non-capacitated sperm demonstrating that mouse sperm enhance both glycolysis and oxidative phosphorylation to support the increasing energy demand during capacitation. The rise in the extracellular acidification rate during sperm capacitation is not affected by the oxidative phosphorylation inhibitors antimycin A and rotenone indicating that the change in this rate is mainly driven by hydrogen release from glycolysis. The increase in oxygen consumption rate, however, is blocked by antimycin A and rotenone as well as by 2-deoxyglucose revealing that the increase in OXPHOS during sperm capacitation is dependent on glycolytic activity.The energy source and pharmacological activators and inhibitors can be varied depending on the goal of the experiment and up to 12 different conditions can be measured in parallel. The protocol can be easily adapted to other species like human or bovine where the changes in energy metabolism during capacitation are equally enigmatic.

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Research

JoVE Journal

Biochemistry

7.7K visualizações.  Weill Cornell Medical College. Este protocolo pode ser usado para aplicar um analisador de fluxo extracelular para monitorar mudanças no metabolismo energético durante a capacitação do esperma. Desenvolvemos este protocolo para comparar mudanças na glicólise e fosforilação oxidativa em tempo real entre espermatozoides não capacitados e capacitados. Na véspera do ensaio, remova o cartucho do sensor de um kit de ensaio de fluxo extracelular e coloque o cartucho de cabeça para baixo ao lado da placa de utilidade.