Sign In

A subscription to JoVE is required to view this content. Sign in or start your free trial.

In This Article

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

Summary

Here, we describe the methodology to knock out a gene of interest in the immune system using clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated endonuclease (Cas9)-based technologies and the evaluation of these mice in a cluster of differentiation 40 (CD40) agonistic antibody-induced colitis model.

Abstract

The immune system functions to defend humans against foreign invaders such as bacteria and viruses. However, disorders of the immune system may lead to autoimmunity, inflammatory disease, and cancer. The inflammatory bowel diseases (IBD)-Crohn's disease (CD) and ulcerative colitis (UC)-are chronic diseases marked by relapsing intestinal inflammation. Although IBD is most prevalent in Western countries (1 in 1,000), incident rates are increasing around the world. Through association studies, researchers have linked hundreds of genes to the pathology of IBD. However, the elaborate pathology behind IBD and the high number of potential genes pose significant challenges in finding the best therapeutic targets. Additionally, the tools needed to functionally characterize each genetic association introduce many rate-limiting factors such as the generation of genetically modified mice for each gene. To investigate the therapeutic potential of target genes, a model system has been developed using clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated endonuclease (Cas9)-based technologies and a cluster of differentiation 40 (CD40) agonistic antibody. The present study shows that CRISPR/Cas9-mediated editing in the immune system can be used to investigate the impact of genes in vivo. Limited to the hematopoietic compartment, this approach reliably edits the resulting reconstituted immune system. CRISPR/Cas9-edited mice are generated faster and are far less expensive than traditional genetically modified mice. Furthermore, CRISPR/Cas9 editing of mice has significant scientific advantages compared to generating and breeding genetically modified mice such as the ability to evaluate targets that are embryonic lethal. Using CD40 as a model target in the CD40 agonistic antibody-induced colitis model, this study demonstrates the feasibility of this approach.

Introduction

Autoimmune diseases refer to conditions in which a patient's immune system attacks their own cells and organs, resulting in chronic inflammation and tissue damage. Nearly 100 different types of autoimmune conditions have been described to date, affecting 3-5% of the human population1. Many of the autoimmune conditions, including systemic lupus erythematosus and IBD, lack effective treatments and present significant unmet medical needs. Currently affecting around 1.5 million people in the USA alone, IBD is a devastating disease marked by progressive, persistent, and relapsing intestinal inflammation with no available cure. Unraveling the und....

Protocol

All animal experiments performed following this protocol must be approved by the respective Institutional Animal Care and Use Committee (IACUC). All procedures described here were approved by the AbbVie IACUC.

1. Generation of required lentiviruses and procurement of donor and recipient animals

NOTE: The Table of Materials includes source and order number details for all animals, instruments, and reagents used in this protocol.

  1. Construct.......

Representative Results

Following the procedure described above, mice expressing CD40-targeted gRNA were generated. By week 2, B-cells, CD11b+ macrophages, and CD11c+ dendritic cells (DCs) were engrafted (Figure 2). T-cells however, as expected based on previous literature18, took longer to fully engraft and required 12 weeks post-engraftment to reach ~90% (Figure 2). Immune organs, such as the spleen and lymph nodes, had the mos.......

Discussion

The results shown here introduce a novel CRISPR/Cas9-based genome editing platform capable of investigating gene function in this CD40 agonistic antibody-induced colitis model. Cell sorting enriched the pool of genetically modified LSK cells, resulting in over 90% reduction in CD40 expression within the reconstituted animals-in just 4 months. Furthermore, the reduced expression of CD40 within the immune system had a profound effect within the CD40 agonistic antibody-induced colitis model, significantly reducing disease e.......

Acknowledgements

Thank you to Ruoqi Peng, Donna McCarthy, Jamie Erikson, Liz O'Connor, Robert Dunstan, Susan Westmoreland, and Tariq Ghayur for your efforts supporting this work. Thank you to Pharmacology leaders including Rajesh Kamath and others for their leadership in establishing the CD40 agonistic antibody-induced colitis model in WT C57Bl/6 mice. Additionally, thank you to all those at AbbVie Bioresearch Center and Cambridge Research Center in the Comparative Medicine East Department supporting in vivo experiments.

We would like to thank the Zhang lab from the Broad Institute and McGovern Institute of Brain Research at the Massachusetts Institute ....

Materials

NameCompanyCatalog NumberComments
6-well tissue culture platesCorning/Costar#3506
TransIT-LT1Mirus BioMIR 2300/5/6
MACS Buffer (autoMACS Running Buffer)Miltenyi Biotec130-091-221
0.45 µm filter unitMillipore#SLHV013SL
0.6 mL microcentrifuge TubeAxygenMCT-060-C-S
1.5 mL Eppendorf TubeAxygenMCT-150-C-S
15mL ConicalVWR21008-918
23 G NeedleVWR#305145
24 Well Non-TC PlatesFalcon#351147
24-Well TC PlatesFalcon#353047
50 mL Conical tubeVWR21008-951
5 mL SyringeBD Biosciences#309647
70 µm FilterMiltenyi#130-098-462
96-Well Flat Bottom PlatesCorning#3599
96-Well U-Bottom PlatesCorning/Costar#3365
Anesthesia MachineVetEquip - COMPAC5#901812
Anti-CD40 Agonist monoclonal antibodyBioXcellBE-0016
Anti-p40 monoclonal antibodyBioXcellBE-0051
B220 PE AntibodyBioLegend#103208
Bovine serum albuminSigma AldrichA7906-100G
Cas9 Knock-in MiceJackson Labs#026179C57Bl/6 background
CD117+ BeadsMiltenyi#130-091-224
CD11b PE AntibodyBioLegend#101208
CD3 PE AntibodyBD Biosciences#553240
CentrifugeBeckman CoulterAllegra 6KR Centrifuge
Countertop CentrifugeEppendorfCentrifuge 5424
DPBSThermoFisher#14190136
Dulbecco’s Modified Eagle MediumMediatech#10-013-CV
Ethylenediamine tetraacetic acid (EDTA)InvitrogenAM9260G
EndoscopeKarl StorzN/ACustom Coloview Tower
Flow cytometerBD BiosciencesFACS Aria II
Fms-related tyrosine kinase 3 ligand (Flt-L)PeproTech#250-31L
Gr-1 PE AntibodyBD Biosciences#553128
Hank's balanced salt solution (HBSS)ThermoFisher#14170120
Heat-Inactivated Fetal Bovine SerumHyClone#SH30071.03
IL-7PeproTech#217-17
IncubatorBinder#9040-0116
IsofluraneHenrySchein#6679401710
LS ColumnMiltenyi#130-042-041
Ly5.1 Pepboy MiceJackson Labs#002014C57Bl/6 background
mouse stem cell factor (mSCF)PeproTech#250-03
Sodium chloride (NaCl)Hospira#00409488850
OPTI-MEM serum-free mediaInvitrogen#31985-070
Penicillin-streptomycin (PenStrep)ThermoFisher#15140-122
Plate ShakerThermoFisher#88880023
pLentiPuroAddgene#52963
Polybrene (10 µg/µL)Sigma Aldrich#TR-1003-G
Red Blood Cell Lysis BuffereBioscience#00-4333
RetronectinTakarbio#T100B
Sca-1 APC AntibodyBioLegend#108112
StemSpanStemCell Technologies#09600
Ter119 PE AntibodyeBioscience#12-5921
Thrombopoietin (TPO)PeproTech#315-14
X-ray IrradiatorPrecision X-RayX-Rad 320

References

  1. Wang, L., Wang, F. S., Gershwin, M. E. Human autoimmune diseases: a comprehensive update. Journal of Internal Medicine. 278 (4), 369-395 (2015).
  2. Uhlig, H. H., Powrie, F. Translating immunology into therapeutic concepts for ....

Explore More Articles

CRISPR Cas9Target Gene FunctionCD40 Agonistic AntibodyColitis ModelInflammatory Bowel DiseaseAutoimmunityGene EditingHematopoietic Compartment

This article has been published

Video Coming Soon

JoVE Logo

Privacy

Terms of Use

Policies

Research

Education

ABOUT JoVE

Copyright © 2024 MyJoVE Corporation. All rights reserved