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Method Article

Functional Assessment of Intestinal Permeability and Neutrophil Transepithelial Migration in Mice using a Standardized Intestinal Loop Model

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DOI:

10.3791/62093

February 11th, 2021

 ,  , 

Corresponding Authors: Anny-Claude Luissint <luissint@med.umich.edu>, Charles A. Parkos <cparkos@med.umich.edu>

In This Article

Summary

Dysregulated intestinal epithelial barrier function and immune responses are hallmarks of inflammatory bowel disease that remain poorly investigated due to a lack of physiological models. Here, we describe a mouse intestinal loop model that employs a well-vascularized and exteriorized bowel segment to study mucosal permeability and leukocyte recruitment in vivo.

Abstract

The intestinal mucosa is lined by a single layer of epithelial cells that forms a dynamic barrier allowing paracellular transport of nutrients and water while preventing passage of luminal bacteria and exogenous substances. A breach of this layer results in increased permeability to luminal contents and recruitment of immune cells, both of which are hallmarks of pathologic states in the gut including inflammatory bowel disease (IBD).

Mechanisms regulating epithelial barrier function and transepithelial migration (TEpM) of polymorphonuclear neutrophils (PMN) are incompletely understood due to the lack of experimental in vivo methods allowing quantitative analyses. Here, we describe a robust murine experimental model that employs an exteriorized intestinal segment of either ileum or proximal colon. The exteriorized intestinal loop (iLoop) is fully vascularized and offers physiological advantages over ex vivo chamber-based approaches commonly used to study permeability and PMN migration across epithelial cell monolayers.

We demonstrate two applications of this model in detail: (1) quantitative measurement of intestinal permeability through detection of fluorescence-labeled dextrans in serum after intraluminal injection, (2) quantitative assessment of migrated PMN across the intestinal epithelium into the gut lumen after intraluminal introduction of chemoattractants. We demonstrate feasibility of this model and provide results utilizing the iLoop in mice lacking the epithelial tight junction-associated protein JAM-A compared to controls. JAM-A has been shown to regulate epithelial barrier function as well as PMN TEpM during inflammatory responses. Our results using the iLoop confirm previous studies and highlight the importance of JAM-A in regulation of intestinal permeability and PMN TEpM in vivo during homeostasis and disease.

The iLoop model provides a highly standardized method for reproducible in vivo studies of intestinal homeostasis and inflammation and will significantly enhance understanding of intestinal barrier function and mucosal inflammation in diseases such as IBD.

Introduction

The intestinal mucosa encompasses a single layer of columnar intestinal epithelial cells (IECs), underlying lamina propria immune cells and the muscularis mucosae. Besides its role in the absorption of nutrients, the intestinal epithelium is a physical barrier that protects the body interior from luminal commensal bacteria, pathogens, and dietary antigens. In addition, IECs and lamina propria immune cells coordinate the immune response inducing either tolerance or response depending on the context and stimuli. It has been reported that the disruption of the epithelial barrier can precede the onset of pathologic mucosal inflammation and contribute to inflammatory bowel....

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Protocol

All animal experiments were conducted in accordance with the guidelines and policies of the National Institutes of Health and approved by the Institutional Animal Care & Use Committee at the University of Michigan.

1. Preoperative preparation

NOTE: This method was generated employing adult mice from C57BL/6 genetic background, aged 8 - 12 weeks. All mice were kept under strict specific pathogen free conditions with ad libitum access to normal chow and water. Results were obtained using C57BL/6, Jam-a - null mice (Jam-a-/-) or mice harboring selective loss of JAM-A on IECs (Villin-cr....

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Results

A schematic representation of the ileal loop and pcLoop models is depicted in Figure 1 and Figure 2, respectively. The anatomical pictures display the critical steps of the procedure including exteriorization of the intestinal segment (Figure 1B and Figure 2B), identification of an appropriate location for ligations that allows minimal disturbance of blood supply (

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Discussion

The mechanisms responsible for dysregulation of intestinal barrier function and immune cell recruitment under pathologic conditions such as IBD are incompletely understood. Here, we detail a robust in vivo murine model that employs a well-vascularized exteriorized intestinal segment of either ileum or proximal colon and allows for assessment of intestinal permeability, neutrophil migration studies as well as other applications.

The iLoop is a non-recovery surgery that is performed on live anim.......

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Disclosures

The authors have nothing to disclose.

Acknowledgements

The authors thank Dr. Sven Flemming of the University of Wuerzburg for his contributions to the establishment of the proximal colon loop model, Sean Watson for the management of the mouse colonies and Chithra K. Muraleedharan for helping with the acquisition of the pictures of the iLoop model. This work was supported by the German Research Foundation/DFG (BO 5776/2-1) to KB, R01DK079392, R01DK072564, and R01DK061379 to C.A.P.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
Equipment and Material
BD Alcohol SwabsBD326895
BD PrecisionGlide Needle, 25G X 5/8"BD305122
BD PrecisionGlide Needle, 30G X 1/2"BD305106
BD 1ml Tuberculin Syringe Without NeedleBD309659
15ml Centrifuge TubeCorning14-959-53A
Corning 96-Well Solid Black Polystyrene MicroplateFisherScientific07-200-592
Corning Non-treated Culture Dish, 10cmMilliporeSigmaCLS430588
Cotton Tip Applicator (cotton swab), 6", sterileFisherScientific25806 2WC
Dynarex Cotton Filled Gauze Sponges, Non-Sterile, 2" x 2"Medex3249-1
EZ-7000 anesthesia vaporizer (Classic System, including heating units)E-Z SystemsEZ-7000
Falcon Centrifuge Tube 50ml VWR21008-940
Fisherbrand Colored Labeling TapeFisherScientific15-901-10R
Halsey Needle Holder (needle holder) FST12001-13
Kimwipes, small (tissue wipe)FisherScientific06-666
1.7ml Microcentrifuge Tubes Thomas Scientific c2170
Micro Tube 1.3ml Z (serum clot activator tube)Sarstedt 41.1501.105
Moria Fine ScissorsFST14370-22
5ml Polystyrene Round-Bottom Tube with Cell-Strainer Cap (35 µm nylon mesh)Falcon352235
Puralube Vet Ointment, Sterile Ocular LubricantDechra12920060
Ring Forceps (blunt tissue forceps)FST11103-09
Roboz Surgical 4-0 Silk Black Braided, 100 YDFisherScientificNC9452680
Semken Forceps (anatomical forceps)FST1108-13
Sofsilk Nonabsorbable Coated Black Suture Braided Silk Size 3-0, 18", Needle 19mm length 3/8 circle reverse cutting HenryScheinSS694
Student Fine Forceps, AngledFST91110-10
10ml Syringe PP/PE without needleMillipore Sigma Z248029
96 Well Cell Culture PlateCorning3799
Yellow Feeding Tubes for Rodents 20G x 30 mmInstechFTP-20-30
Solutions and Buffers
Accugene 0.5M EDTALonza51201
Ammonium-Chloride-Potassium (ACK) Lysing BufferBioWhittaker10-548E
Hanks' Balanced Salt SolutionCorning21-023-CV
Phosphate-Buffered Saline without Calcium and MagnesiumCorning21-040-CV
Reagents
Alexa Fluor 647 Anti-Mouse Ly-6G Antibody (1A8)BioLegend127610
CD11b Monoclonal Antibody, PE, eBioscience (M1/70)ThermoFisher12-0112-81
CountBright Absolute Counting BeadsInvitrogenC36950
DithiotreitolFisherScientificBP172-5
Fetal Bovine Serum, heat inactivatedR&D Systems511550
Fluorescein Isothiocyanate-Dextran, average molecular weight 4.000Sigma60842-46-8
IsofluraneHalocarbon12164-002-25
Leukotriene B4Millipore Sigma71160-24-2
PerCP Rat Anti-Mouse CD45 (30-F11)BD Pharmingen557235
Purified Rat Anti-Mouse CD16/CD32 (Mouse BD FC Block)BD Bioscience553142
Recombinant Murine IFN-γPeprotech315-05
Recombinant Murine TNF-αPeprotech315-01A

References

  1. Olson, T. S., et al. The primary defect in experimental ileitis originates from a nonhematopoietic source. Journal of Experimental Medicine. 203 (3), 541-552 (2006).
  2. Jump, R. L., Levine, A. D. M....

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Tags

Neutrophil MigrationEpithelial BarrierTight JunctionsFITC Dextran AssayInflammatory Bowel DiseaseFlow CytometryJAM A Protein