Name: Cecal Ligation and Puncture-induced Sepsis as a Model To Study Autophagy in Mice (Video) | JoVE Journal
Uploaded: 2014-02-09T22:00:00.000+00:00
Duration: 6 min 40 s
Description: Learn the cecal ligation and puncture method to induce sepsis in mice for studying tissue autophagy. This protocol enables researchers to visualize autophagosome formation using electron microscopy.

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This work was supported by NIH grants P01 HL108801, R01-HL60234, R01-HL55330, R01-HL079904, to A. M. K. Choi. S. Ryter received salary support from the Lovelace Respiratory Research Institute.

Note:&#160; The Institutional Animal Care and Use Committee at Brigham and Women&#39;s Hospital/ Harvard Medical School Area approved the following procedures.
1. Cecal Ligation and Puncture
Use mice of the same background (C57Bl/6), male, 8-10 weeks old. Female mice are more resistant than males against sepsis-induced lethality. Mice older than 8 weeks produce less variable results than younger mice in terms of survival after CLP. Approximately N=10 mice per compared group should be used for survival analysis. N=3-5 mice is adequate for autophagy assays.
<ol>
	<li>Use sterile small surgical instruments (namely scalpel, scissors and blunt anatomical forceps), which should be appropriate for rodent surgery.</li>
	<li>Prepare anesthesia mixture: To 7.95 ml of PBS add 150 &#956;l of Xylazine (AnaSed injection&#160;100 mg/ml) and 700 &#956;l of Ketamine (Ketaset&#160;CIII, 100 mg/ml).</li>
	<li>To ensure aseptic conditions during the procedure, wear gloves, face mask and surgical gown.</li>
	<li>Weigh animals. Anesthetize them by injecting intraperitonally (i.p.) the mixture mentioned in step 3 in a dosage of &#956;l&#160;(10x body weight in g) . For example, for a mouse weighing 22 g, administer 10x22= 220 &#956;l of the anesthetic mixture. Thus, the final doses of Xylazine and Ketamine are 17 and 80 mg/kg body weight, respectively. Ensure that anesthesia is adequate; no flexion of extremity should be produced after toe pinch. Note: Use ophthalmic&#160;ointment on eyes to prevent dryness while under anesthesia.</li>
	<li>Place animals onto a clean work surface on their backs. Tails and hind paws are oriented towards the investigator. Disinfect the abdominal skin using alcohol (70% EtOH solution). Note: Surgical area should be completely shaved, to avoid contamination of the wound through contact with fur.&#160;Also, optimally, a circulating warm water pad should be used to maintain normothermia of anesthetized mice during the surgery.</li>
	<li>By using a scalpel, make a small longitudinal skin incision parallel and approximately 1 cm left to midline. Do not penetrate yet into the peritoneal cavity. Use small scissors to extend the initial incision.</li>
	<li>Identify abdominal muscles and dissect them to gain access into the peritoneal cavity.</li>
	<li>By using blunt anatomical forceps, identify the cecum and move it out of the peritoneal cavity. Be careful not to damage mesenterial blood vessels (this could lead to lethal hemorrhage).</li>
	<li>Ligate 60% of the cecum to achieve a mid-grade sepsis. Ligating equal to or more than 75% of the cecum generally results in high-grade sepsis, whereas ligating equal to or less than 25% of the cecum results in low-grade sepsis. Be careful not to ligate the ileocecal valve (this could block the intestinal continuity).</li>
	<li>By using a 21&#160;G needle, perforate the cecum by one through-and-through puncture (two holes) near to the ligation. The direction of the perforation should be from the mesenteric to the anti-mesenteric side of the cecum. Be careful not to puncture mesenterial blood vessels.</li>
	<li>Remove the needle. Gently squeeze the ligated cecum to confirm patency through the two holes; only a small amount of feces should be extruded through them.</li>
	<li>Move the ligated and punctured cecum into the peritoneal cavity. Note: For sham mice, skip steps 1.10-1.12.</li>
	<li>Use silk surgical sutures 6-0 with cutting needle to close abdominal musculature. Use silk surgical sutures 6-0 with cutting needle to close abdominal skin.</li>
	<li>Inject 1 ml&#160;prewarmed (37 &#176;C) normal saline i.p. to replace heat and hydration lost during the procedure. Place the mice under a heat lamp until their resuscitation.&#160;Note: Optimally, a safer warming device (such as a circulating warm water pad) can be used instead of a heat lamp.</li>
	<li>Postoperatively inject buprenorphin (0.05 mg/kg body weight s.c.) to achieve analgesia. Note: An animal should not be left unattended until it has regained sufficient consciousness to maintain sternal recumbency. An animal which has undergone a surgical treatment should not be returned to the company of other animals until fully recovered.</li>
	<li>Place animals back in their cages with unlimited access to food and water. Mice will be euthanized when they become moribund (indicated by clinical signs such as failure to move when touched or cyanosis). Check mice every 4 hr&#160;to avoid having them die prior to euthanasia.</li>
</ol>
2. Tissue Harvest and Fixation
<ol>
	<li>Prepare a 4% paraformaldehyde (PFA) solution: To 889 ml PBS add 111 ml of 37% PFA.</li>
	<li>Sacrifice mice using either CO2-induced narcosis or Ketamine/Xylazine solution in a high dosage.</li>
	<li>Immobilize the mice onto a clean work surface. Spray the abdominal and thoracic skin with 70% EtOH solution to disinfect it.</li>
	<li>Use a scalpel and small scissors to remove the abdominal and thoracic skin as well as the skin covering the tracheal area.</li>
	<li>Reveal trachea by removing its surrounding tissues (muscles and connective tissue).</li>
	<li>Place a suture (without cutting needle) around the trachea. Do not tighten it yet.</li>
	<li>Use a small peripheral venous catheter (20 G) to &#39;intubate&#39; trachea. Be careful during the catheter insertion to avoid tracheal tear. Note that the largest diameter of trachea is just below the cricoid cartilage.</li>
	<li>Tighten the suture around the trachea/catheter. Remove the needle leaving only the plastic cannula of the catheter into the trachea. Needle served only as a guide-wire for inserting the plastic cannula.</li>
	<li>After having secured the plastic cannula into the trachea, cut the abdominal musculature, open the abdomen and reveal the diaphragm.</li>
	<li>Using a needle, puncture the diaphragm to produce pneumothorax (i.e.&#160;insertion of air into the pleural cavity). Lungs should then be collapsed.</li>
	<li>Using small scissors, remove the diaphragm, cut along the sternum (sternotomy), remove the rib cage and reveal the heart and the lungs.</li>
	<li>Through the plastic cannula inserted into the trachea, fix the lungs with the formaldehyde solution under 30 cm H2O pressure.</li>
	<li>Remove the lungs and place them into the 4% PFA for 24 hr and subsequently in 70% EtOH solution until processing.</li>
	<li>Identify and remove heart, liver and kidneys. In the same way, place them into the 4% PFA for 24 hr and subsequently in 70% EtOH solution until processing.</li>
</ol>
3. GFP Mice and Viewing of GFP Slides
<ol>
	<li>Perform CLP and sham surgery on GFP-LC3 mice as described in step 1, and postoperative procedures as described in step 2 of the protocol.</li>
	<li>Embed the tissues (namely lungs, heart, liver and kidneys) in paraffin and cut them in serial 5&#160;&#956;m sections.</li>
	<li>When ready for GFP staining, incubate at 60 &#176;C for 30-60 min until paraffin melts and tissue appears translucent.</li>
	<li>Deparaffinize with standard graded series of xylene or xylene substitutes, 5 min xylene 1, xylene 2, and xylene 3 then 3 min incubations in graded series of EtOH: 100%, 95%, 75%, and then rinse in distilled water. 
	Note: After deparaffinization avoid tissue desiccation, which increases sample background.</li>
	<li>Perform antigen retrieval using citric acid buffer (10 mM sodium citrate acid, 0.05% Tween 20, pH 6.0), by microwaving for 10-20 min. Be careful to replace buffer periodically to avoid tissue desiccation.</li>
	<li>Allow solution to cool for 20 min on the bench to complete antigen retrieval.</li>
	<li>Wash 2-3x with PBS. Remove excess buffer and transfer slides from rack to horizontal position in a slide box or other humidified chamber to prevent desiccation.</li>
	<li>Block 45-60 min at room temperature with 10% normal donkey serum (also 5% bovine serum albumin, or preferably serum from the animal in which the secondary antibody was generated) in PBS.</li>
	<li>Incubate samples in primary GFP antibody at 1:100 dilution in PBS overnight at 4 &#176;C in humidified chamber. Gently apply small pieces of Parafilm over tissue with antibody to promote homogenous contact with the tissue and prevent evaporation. 
	Note: Remaining steps are performed at room temperature.</li>
	<li>Wash 5x with PBS to remove excess primary antibody. Incubate with secondary antibody 1:500-1:1,000 in PBS for 1-2 hr at room temperature.</li>
	<li>Wash 5x with PBS to remove excess secondary antibody. If desired, counterstain the slides at this step.</li>
	<li>If using fluorescent secondary antibody, incubate 0.1% Sudan Black in 70% EtOH for 15-20 min to reduce autofluorescence. Wipe off excess Sudan Black from around tissue and wash 5x with PBS over 20 min.</li>
	<li>Mount sample with coverslip and store horizontally, until mounting solution has set.</li>
</ol>
4. Alternative Protocol: Direct Detection of GFP-LC3
<ol>
	<li>Cannulate and inflate lungs with a ~500 ml of 50/50 v/v OCT PBS.</li>
	<li>Embed in OCT by putting a small amount of OCT in the bottom of a cryomold.</li>
	<li>Carefully place the dissected lung complex in the mold.</li>
	<li>Slowly freeze over methylbutane chilled using dry ice.</li>
	<li>Add more OCT until the tissue is completely covered and frozen solid. Keep on dry ice and store at -80 &#176;C.</li>
	<li>Using a cryomicrotome, cut 5-10 &#956;m thick sections protecting the sections from light. Store sections and remaining tissue at -80 &#176;C.</li>
	<li>To prepare slides for imaging, remove section from freezer and immediately apply a drop of PBS to prevent desiccation.</li>
	<li>Fix for 30 min with 4% PFA. Wash with PBS.</li>
	<li>Apply DAPI/Hoescht for 10 min. Wash 3x&#160;with PBS.</li>
	<li>Mount sample with coverslip and store horizontally, until mounting solution has set.</li>
	<li>Image using epifluorescence or confocal microscope.&#160;Store samples at 4 &#176;C for up to one month.</li>
</ol>
5. Preparation of Tissue for Electron Microscopy
<ol>
	<li>Cut tissues into approximately 1 mm cubes for fixing.</li>
	<li>Fix the tissue in 2% formaldehyde, 2.5% glutaraldehyde in 0.1 M sodium cacodylate buffer, pH 7.4.</li>
	<li>Wash with 0.1 M sodium cacodylate buffer for 1-2 hr. 
	Note: Fixed tissue can be stored in 0.1 M sodium cacodylate at 4 &#176;C.</li>
	<li>Post fix in 1% osmium tetroxide in 0.2 M sodium cacodylate buffer for 1 hr.</li>
	<li>Rinse in 0.2 M sodium cacodylate buffer for 10 min 3x.</li>
	<li>Dehydrate in 70% EtOH, 20 min 2x. Dehydrate in 90% EtOH, 10 min 2x. Dehydrate in 100% EtOH, 20 min 2x.</li>
	<li>Incubate with propylene oxide (epoxy propane) for 10 min 2x.</li>
	<li>Incubate with propylene oxide/epoxy resin mixture (50:50) for 1 hr. The epoxy resin mixture is: 24 g Agar 100 resin, 13 g dodecenylsuccinic anhydride, 13 g methylnadic anhydride and 1 ml N-benzyldimethylamine. Mix thoroughly in a disposable beaker using a wooden spatula.</li>
	<li>Incubate with Epoxy resin overnight in uncapped vials (this allows any remaining propylene oxide to evaporate).</li>
	<li>Embed in labeled capsules with freshly prepared resin. Polymerize at 60 &#176;C for 48 hr.</li>
	<li>Photograph tissue sections using a transmission electron microscope at 80 or 60 kV onto electron microscope film. Print the images onto photographic paper or store as digital media.</li>
	<li>Analyze autophagosome formation in intact cells containing nucleus. Low power fields (e.g. 2,000-4,000X) can be used to identify nucleated cells. Typically 6,800-10,000X images are used for this autophagosome quantification. Count autophagosomes per unit area from 15-30 fields for appropriate statistical representation. Autophagosomes have double membrane structure, where late stage autophogosomes resembled filled vacuoles.</li>
</ol>

<ol><li>Hotchkiss, R. S., Karl, I. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((The+pathology+and+treatment+of+sepsis%5BTitle%5D)+AND+%22N.+Engl.+J.+Med%22%5BJournal%5D)">The pathology and treatment of sepsis.</a> N. Engl. J. Med. 348, 138-150 (2003).</li>
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<li>Haspel, J., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Characterization+of+macroautophagic+flux+in+vivo+using+a+leupeptin-based+assay%5BTitle%5D)+AND+%22Autophagy%22%5BJournal%5D)">Characterization of macroautophagic flux in vivo using a leupeptin-based assay.</a> Autophagy. 7, 629-642 (2011).</li>
<li>Chen, Z. H., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Egr-1+regulates+autophagy+in+cigarette+smoke-induced+chronic+obstructive+pulmonary+disease%5BTitle%5D)+AND+%22PLos+One%22%5BJournal%5D)">Egr-1 regulates autophagy in cigarette smoke-induced chronic obstructive pulmonary disease.</a> PLos One. 3, 3313 (2008).</li>
<li>Kim, H. P., Chen, Z. H., Choi, A. M., Ryter, S. W. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Analyzing+autophagy+in+clinical+tissues+of+lung+and+vascular+diseases%5BTitle%5D)+AND+%22Meth.+Enzymol%22%5BJournal%5D)">Analyzing autophagy in clinical tissues of lung and vascular diseases.</a> Meth. Enzymol. 453, 197-216 (2009).</li>
<li>Flierl, M. A., et al. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Adverse+functions+of+IL-17A+in+experimental+sepsis%5BTitle%5D)+AND+%22FASEB+J%22%5BJournal%5D)">Adverse functions of IL-17A in experimental sepsis.</a> FASEB J. 22, 2198-2205 (2008).</li>
<li>Rittirsch, D., Huber-Lang, M. S., Flierl, M. A., Ward, P. A. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Immunodesign+of+experimental+sepsis+by+cecal+ligation+and+puncture%5BTitle%5D)+AND+%22Nat.+Protoc%22%5BJournal%5D)">Immunodesign of experimental sepsis by cecal ligation and puncture.</a> Nat. Protoc. 4, 31-36 (2009).</li>
<li>Mizushima, N., Yoshimori, T., Levine, B. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Methods+in+mammalian+autophagy+research%5BTitle%5D)+AND+%22Cell%22%5BJournal%5D)">Methods in mammalian autophagy research.</a> Cell. 140, 313-326 (2010).</li>
<li>Wang, L., Ma, R., Flavell, R. A., Choi, M. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Requirement+of+mitogen-activated+protein+kinase+kinase+3+%28MKK3%29+for+activation+of+p38%CE%B1+and+p38%CE%B4+MAPK+isoforms+by+TGF-%CE%B21+in+murine+mesangial+cells%5BTitle%5D)+AND+%22J.+Biol.+Chem%22%5BJournal%5D)">Requirement of mitogen-activated protein kinase kinase 3 (MKK3) for activation of p38α and p38δ MAPK isoforms by TGF-β1 in murine mesangial cells.</a> J. Biol. Chem. 277, 47257-47262 (2002).</li>
<li>Ding, Y., Kim, J. K., Kim, S. I., Na, H. J., Jun, S. Y., Lee, S. J., Choi, M. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((TGF-%7Bbeta%7D1+protects+against+mesangial+cell+apoptosis+via+induction+of+autophagy%5BTitle%5D)+AND+%22J+Biol+Chem%22%5BJournal%5D)">TGF-{beta}1 protects against mesangial cell apoptosis via induction of autophagy.</a> J Biol Chem. 285, 37909-37919 (2010).</li>
<li>Baker, C. C., Chaudry, I. H., Gaines, H. O., Baue, A. E. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Evaluation+of+factors+affecting+mortality+rate+after+sepsis+in+a+murine+cecal+ligation+and+puncture+model%5BTitle%5D)+AND+%22Surgery%22%5BJournal%5D)">Evaluation of factors affecting mortality rate after sepsis in a murine cecal ligation and puncture model.</a> Surgery. 94, 331-335 (1983).</li>
<li>Godshall, C. J., Scott, M. J., Peyton, J. C., Gardner, S. A., Cheadle, W. G. <a target="_blank" href="http://www.ncbi.nlm.nih.gov/pubmed?term=((Genetic+background+determines+susceptibility+during+murine+septic+peritonitis%5BTitle%5D)+AND+%22J.+Surg.+Res%22%5BJournal%5D)">Genetic background determines susceptibility during murine septic peritonitis.</a> J. Surg. Res. 102, 45-49 (2002).</li>
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</ol>

The authors have no competing financial interests to declare

The major advantage of CLP is that it allows researchers to investigate sepsis of different severities (i.e.&#160;from low- to mid- and high-grade). Severity of induced sepsis is affected by the length of cecum ligated (which the most important determinant), the size of needle used for puncture and the number of holes performed15. In addition, the mouse strain and gender can impact on the severity of sepsis; several strains are more susceptible than others and males are generally more susceptible than...

Sepsis, a systemic inflammatory response to infection, represents a leading cause of death in critically-ill patients1. Intra-abdominal infections, often leading to polymicrobial sepsis, account for 20% of sepsis cases, which have substantial mortality of up to 60%2. Sepsis-associated mortality primarily results from multi-organ dysfunction with subsequent organ failure3,4. Additional investigation into the pathogenic mechanism of this disease is urgently needed to promote the development of novel and more effective therapies.
The cecal ligation and puncture (CLP) method is a commonly used procedure for modeling sepsis in vivo. As the cecum is full of bacteria, its puncture results in polymicrobial peritonitis, translocation of bacteria into the blood (bacteremia), septic shock, multi-organ dysfunction and, ultimately, death5. It is generally accepted that CLP reflects clinical reality more accurately than previous techniques, such as injection of endotoxin or even purified bacteria into rodents, Thus, CLP is considered the gold standard (albeit not without limitations)6 for the experimental induction and, hence, the investigation of the pathogenesis of sepsis. In this monograph, we describe protocols designed to assess whether pathogenic mechanisms of sepsis include autophagy.
Autophagy, an evolutionarily conserved cellular process, facilitates the turnover of damaged proteins and organelles such as mitochondria and plays an important role in the clearance of intracellular pathogens including bacteria7,8. During autophagy, cytosolic proteins or organelles are sequestered into double membrane-bound vesicles called autophagosomes, which are subsequently delivered to the lysosomes for degradation9. A number of proteins have been identified as the mammalian homologues of autophagy-related genes (Atg), originally identified in yeast, which regulate the process of autophagy. The conversion of microtubule associated protein-1 light chain 3B (LC3B) (homologue of Atg8) from LC3B-I (free form) to LC3B-II (phosphatidylethanolamine-conjugated form) represents a major step in autophagosome formation9. Autophagic dysfunction is associated with aging and human diseases including cancer and neurodegenerative disorders10. Moreover, autophagy affects innate and adaptive immunity such as antigen presentation, lymphocyte development and cytokine secretion by immune cells8. Thus, it seems reasonable that autophagy might also play a role in the systemic inflammatory response to infection (i.e.&#160;in sepsis).
To date several methods have been described to assess the role of autophagy in tissue injury in vivo. These include the use of green fluorescence protein (GFP)-LC3 expressing mice&#160;and the quantification of autophagosomes in tissue by electron microscopy&#160;(these two methods are described in this monograph). Additional methods include the quantification of autophagic protein expression in tissue homogenates, and the analysis of autophagic flux (as described elsewhere)11-13. The goal of this review is to provide current protocols for assessing autophagy in vivo in the context of experimental sepsis.

<table><tbody><tr><td>GFP-LC3 Transgenic Mice</td><td>Riken (Japan)</td><td>RBRC00806</td><td>GFP-LC3#53</td></tr><tr><td>Xylazine</td><td>Henry-Schein</td><td>568-0606</td><td>Xylazine HCl Injection Vet</td></tr><tr><td>Ketamine</td><td>Henry-Schein</td><td>995-2949</td><td>Ketaset Inj 100 mg/ml</td></tr><tr><td>EtOH</td><td>Fisher</td><td>A405-20</td><td>Histology Grade</td></tr><tr><td>EtOH</td><td>Fisher</td><td>A407-1</td><td>For Sterilizatiion</td></tr><tr><td>silk surgical sutures 6-0</td><td>Owens &amp;amp; Minor</td><td>2300-0078OG, 017624</td><td></td></tr><tr><td>buprenorphine-HCl</td><td>Henry-Schein</td><td>614-5157</td><td>Buprenex Ampules</td></tr><tr><td>paraformaldehyde (37%) solution</td><td>JT Baker</td><td>S898-09</td><td></td></tr><tr><td>xylenes</td><td>Fisher</td><td>X3P-1GAL </td><td></td></tr><tr><td>anti-GFP monoclonal antibody</td><td>Life Technologies</td><td>G10362</td><td></td></tr><tr><td>Hoescht</td><td>Sigma</td><td>944403</td><td></td></tr><tr><td>DAPI</td><td>Invitrogen</td><td>D1306</td><td></td></tr><tr><td>OCT</td><td>VWR scientific</td><td>25608-930</td><td></td></tr><tr><td>Sudan Black</td><td>Santa Cruz</td><td>sc-203760</td><td></td></tr><tr><td>EM grade Glutaraldehyde 2.5% in sodium cacodylate</td><td>Electron microscopy Sciences</td><td>15960</td><td></td></tr><tr><td>propylene oxide</td><td>Sigma</td><td>240397</td><td></td></tr><tr><td>Agar 100 resin</td><td>Agar scientific</td><td> R1045</td><td></td></tr><tr><td>dodecenylsuccinic anhydride</td><td>Sigma</td><td>46346</td><td></td></tr><tr><td>methylnadic anhydride</td><td>Sigma</td><td>45359</td><td></td></tr><tr><td>N-benzyldimethylamine</td><td>Sigma</td><td>185582</td><td></td></tr></tbody></table>

cecal ligation and puncture-induced sepsis as a model to study autophagy in mice

Cecal Ligation and Puncture-induced Sepsis as a Model To Study Autophagy in Mice

Experimental sepsis can be induced in mice using the cecal ligation and puncture (CLP) method, which causes polymicrobial sepsis. Here, a protocol is provided to induce sepsis of varying severity in mice using the CLP technique. Autophagy is a fundamental tissue response to stress and pathogen invasion. Two current protocols to assess autophagy in vivo in the context of experimental sepsis are also presented here. (I) Transgenic mice expressing green fluorescence protein (GFP)-LC3 fusion protein are subjected to CLP. Localized enhancement of GFP signal (puncta), as assayed either by immunohistochemical or confocal assays, can be used to detect enhanced autophagosome formation and, thus, altered activation of the autophagy pathway. (II) Enhanced autophagic vacuole (autophagosome) formation per unit tissue area (as a marker of autophagy stimulation) can be quantified using electron microscopy. The study of autophagic responses to sepsis is a critical component of understanding the mechanisms by which tissues respond to infection. Research findings in this area may ultimately contribute towards understanding the pathogenesis of sepsis, which represents a major problem in critical care medicine.

Bacteremia is present in mice as early as 6 hr after CLP-induced sepsis14. Clinical signs of sepsis (including chills, tachypnoea and impaired motor activity) appear approximately 12 hr after the procedure. Mice subjected to CLP begin to die at around 18 hr after induction of peritonitis. The more severe is the sepsis the more increased is the lethality15. In detail, high-grade sepsis causes 100% mortality within 2-3 days, while mid-grade sepsis results in around 60% mortality at 7 days after CLP (b...

Experimental sepsis can be induced in mice using the cecal ligation and puncture (CLP) method. Current protocols to assess autophagy in vivo in the context of CLP-induced sepsis are presented here: A protocol for measuring autophagy using (GFP)-LC3 mice, and a protocol for measuring autophagosome formation by electron microscopy.

Experimental sepsis can be induced in mice using the cecal ligation and puncture (CLP) method, which causes polymicrobial sepsis. Here, a protocol is ...

The overall goal of this procedure is to induce sepsis through seql ligation and puncture in mice in order to study tissue autophagy, a homeostatic process that facilitates turnover of damaged proteins and organelles. This is accomplished by first identifying the secum and moving it out of the peritoneal cavity of the anesthetized mouse. Once isolated, 60%of the secum is ligated and then perforated to induce mid-grade peritonitis.The ligated and punctured seum is placed back into the peritoneal cavity and the animal is allowed to recover. The final step is to harvest the lung, liver, and kidney tissues from the septic animal 24 hours later. Ultimately, electron microscopy is used to show autophagosome formation in intact cells from the tissues harvested from the septic animal.We will present sickle ligation and punctu or CLP as a means to induce sepsis and to study autophagy. The main advantage of this technique over previous methods like injection of endotoxin, is its clinical relevance. CLP leads to peritonitis, which is a well-known cause of polymicrobial sepsis in humans.Autophagy represents a general stress response in tissues that may be activated by starvation or bacterial i

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Research

JoVE Journal

Immunology and Infection

The mouse model of cecal ligation and puncture as a valuable tool for the study of human sepsis.

Cecal Ligation Puncture Procedure

Sepsis refers to a systemic inflammatory response syndrome resulting from a microbial infection, and can be simulated by a surgical technique termed cecal ligation and puncture (CLP).  Here we describe a method to use CLP-induced animal model to screen medicinal herbs for therapeutic agents.

Use of Animal Model of Sepsis to Evaluate Novel Herbal Therapies

To counteract pathogen dissemination, host cells reorganize their cytoskeleton to compartmentalize bacteria and induce autophagy. Using Shigella infection of tissue culture cells, host and pathogen determinants underlying this process are identified and characterized. Using zebrafish models of Shigella infection, the role of discovered molecules and mechanisms are investigated in vivo.

Use of Shigella flexneri to Study Autophagy-Cytoskeleton Interactions

Here a protocol to mimic the entrance of bacterial-derived compounds after intestinal barrier breach is presented. A low sublethal dose of lipopolysaccharide was injected systemically into mice, which were monitored for 24 h post-injection. The expression of pro-inflammatory cytokines was determined at several time points in spleen, liver, and colon.

Injections of Lipopolysaccharide into Mice to Mimic Entrance of Microbial-derived Products After Intestinal Barrier Breach

Here a simple and well-validated protocol for measuring bulk autophagic sequestration activity in mammalian cells is described. The method is based on quantifying the proportion of lactate dehydrogenase (LDH) in sedimentable cell fractions compared to total cellular LDH levels.

The Lactate Dehydrogenase Sequestration Assay &#8212; A Simple and Reliable Method to Determine Bulk Autophagic Sequestration Activity in Mammalian Cells

This protocol describes techniques to measure infectious outcomes underlying secondary hospital-acquired infections in the immunosuppressive condition, first by establishing cecal ligation/puncture mice then challenging them with intranasal infection to create a clinically relevant model of immunosuppression sepsis.

Design of Cecal Ligation and Puncture and Intranasal Infection Dual Model of Sepsis-Induced Immunosuppression

This protocol presents the operative details of cecal ligation and puncture (CLP) in a mouse model of sepsis. CLP is one of the most widely used techniques to create an animal model of sepsis. Therefore, a standardized CLP protocol is required for the attainment of reliable research results.

Evaluation of a Reliable Biomarker in a Cecal Ligation and Puncture-Induced Mouse Model of Sepsis

This protocol describes the induction of Gram-negative monobacterial sepsis in a mouse model system. The model is useful in investigating the inflammatory and lethal host responses during sepsis.

Characterizing Salmonella Typhimurium-induced Septic Peritonitis in Mice

This murine model combines a septic insult with hindlimb muscle disuse to recapitulate the bedridden feature of the typical septic patient. The model represents a significant departure from previous models to study muscle dysfunction in sepsis and is a reproducible approach to addressing therapeutic strategies to treat this condition.

A Preclinical Model of Sepsis-Induced Myopathy with Disuse in Mice

Here, we present a protocol for establishing a mouse sepsis immunosuppression model via intranasal instillation of Klebsiella pneumoniae and validated the model through various indicators.

Establishment of A Mouse Sepsis-Induced Immunosuppression Model By Intranasal Instillation of Bacteria

Learn the cecal ligation and puncture method to induce sepsis in mice for studying tissue autophagy. This protocol enables researchers to visualize autophagosome formation using electron microscopy.

Cecal Ligation and Puncture-induced Sepsis as a Model To Study Autophagy in Mice

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