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In This Article

  • Summary
  • Abstract
  • Introduction
  • Protocol
  • Representative Results
  • Discussion
  • Acknowledgements
  • Materials
  • References
  • Reprints and Permissions

Summary

The goal of this protocol is to isolate mononuclear cells that reside in the lamina propria of the colon by enzymatic digestion of the tissue using collagenase. This protocol allows for the efficient isolation of mononuclear cells resulting in a single cell suspension which in turn can be used for robust immunophenotyping.

Abstract

The intestine is the home to the largest number of immune cells in the body. The small and large intestinal immune systems police exposure to exogenous antigens and modulate responses to potent microbially derived immune stimuli. For this reason, the intestine is a major target site of immune dysregulation and inflammation in many diseases including but, not limited to inflammatory bowel diseases such as Crohn’s disease and ulcerative colitis, graft-versus-host disease (GVHD) after bone marrow transplantation (BMT), and many allergic and infectious conditions. Murine models of gastrointestinal inflammation and colitis are heavily used to study GI complications and to pre-clinically optimize strategies for prevention and treatment. Data gleaned from these models via isolation and phenotypic analysis of immune cells from the intestine is critical to further immune understanding that can be applied to ameliorate gastrointestinal and systemic inflammatory disorders. This report describes a highly effective protocol for the isolation of mononuclear cells (MNC) from the colon using a mixed silica-based density gradient interface. This method reproducibly isolates a significant number of viable leukocytes while minimizing contaminating debris, allowing subsequent immune phenotyping by flow cytometry or other methods.

Introduction

Though the gastrointestinal (GI) tract is primarily dedicated to the processing and reabsorption of nutrients from food, the GI tract also maintains central roles in the integrity of the vascular, lymphatic, and nervous systems and of numerous other organs through its mucosal and submucosal immune system1. The GI immune system has an influential role in both gastrointestinal and systemic health due to its constant exposure to foreign antigens from food, commensal bacteria, or invading pathogens1,2. Thus, the GI immune system must maintain a delicate balance in which it tolerates non-pat....

Protocol

All studies were conducted under rodent research protocols reviewed and approved by the Institutional Animal Care and Use Committee (IACUC) of the University of Miami Miller School of Medicine, which meets the veterinary standards set by the American Association for Laboratory Animal Science (AALAS).

1. Preparation of Solutions

  1. As described in Table 1, prepare the Colon Buffer, Silica-Based Density Separation Media 100%, Silica-Based Density Separation Media 66%, Silica-bas.......

Representative Results

When working with murine colon disease models, it is helpful to be able to both quantify and qualitatively assess, among the MNC of the colon, multiple immune cell subsets involved in the inflammatory process. The single-cell suspension of MNC obtained through the application of this protocol facilitates such phenotypic characterization in a robust and reproducible manner. As a proof of principle for the application of this isolation method under diverse experimental settings, we retrieve.......

Discussion

This visual protocol describes well-tolerated methods for the isolation of colonic mononuclear cells including lamina propria lymphocytes (LPL). Given that this protocol was optimized in evaluating severe post-transplant mouse colitis models where inflammatory cytokines and tissue injury lend themselves to poor viability of recovered MNC, we anticipate that these methods can be translated to other applications requiring phenotypic analysis of colonic MNC. These include but, are not limited to assessing colon inflammation.......

Acknowledgements

This work was supported by grants #1K08HL088260 and #1R01HL133462-01A1 (NHLBI) (A.B.P., H.N., S.J.), and the Batchelor Foundation for Pediatric Research (D.M., H.N., S.J., A.A.H., A.B.P.). C57BL/6 and BALB/c mice used in this study were either bred in our facility or provided by Jackson Labs or Taconic.

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Materials

NameCompanyCatalog NumberComments
60 mm Petri DIshThermo Scientific150288
1x PBSCorning21-040-CV
10x PBSLonza BioWhittakerBW17-517Q
10 mL Disposable Serological PipetteCorning4100
10mL SyringeBecton Dickinson302995
15mL Non-Sterile Conical TubesTruLineTR2002
18- gauge Blunt NeedleBecton Dickinson305180
25 mL Disposable Serological PipetteCorning4250
40 micrometer pore size Cell StrainerCorning352340
50 mL Falcon TubeCorning21008-951
Bovine Serum Albumin (BSA)SigmaA4503-1KG
Fixation BufferBiolegend420801
E. coli Collagenase E from Clostridium histolyticumSigmaC2139
EDTA, 0.5M Sterile SolutionAmrescoE177-500ML
Fetal Bovine SerumThermo /Fisher Scientific -HyCLoneSV30014.03
HEPESGE Healthcare-HyCloneSH30237.01
PercollGE Healthcare-Life Sciences1708901
RPMI MediumCorning17-105-CV
Sodium AzideVWR Life Science Amresco97064-646
Trypan BlueLonza BioWhittaker17-942E

References

  1. Schneeman, B. Gastrointestinal physiology and functions. British Journal of Nutrition. 88, S159-S163 (2002).
  2. Arranz, E., Pena, A. S., Bernardo, D. Mediators of inflammation and immune responses in the human gastrointestinal trac....

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ColonLamina PropriaMononuclear CellsCollagenaseImmune CellsIntestineInflammationMouse ModelsCancerAllergyTransplantationAutoimmunityPhenotypic AnalysisFlow Cytometry

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