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Method Article

A Cryo-pulverization Protocol for Processing Mouse Paws to Evaluate Molecular Pathways of Tissue Inflammation in a Collagen Induced Arthritis Model

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DOI:

10.3791/60229

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October 30th, 2019

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In This Article

Summary

A cryogenic pulverization method to process murine paws using a liquid nitrogen freezer mill was developed to improve the yield and quality of RNA or protein extracted from the tissues and enable the analysis of molecular profiles associated with inflammatory responses.

Abstract

Profiling molecular changes in local tissues is crucial to understand the mechanism(s) of action of therapeutic candidates in vivo. In the field of arthritis research, many studies are focused on inflamed joints that are composed of a complex mixture of bone, cartilage, muscle, stromal cells and immune cells. Here, we established a reliable and robust mechanical method to disrupt inflamed mouse paws into homogeneous pulverized samples in a cryogenically controlled environment. Protein and RNA lysates were processed to enable proteomic and transcriptional endpoints and molecular characterization of relevant disease pathways in local tissue.

Introduction

Rheumatoid arthritis (RA) is a chronic systemic inflammatory disease with persistent symmetric synovitis in joints and extra articular involvement of organs such as the skin, heart, lungs, and eyes1. Although the systemic manifestations of the immune response are evident in human patients, one of the hallmarks of RA pathology is infiltration of immune cells in synovial tissue and proliferation of synovial fibroblast cells2.

Similar to human RA, mouse collagen induced arthritis (CIA) model elicits strong tissue inflammation with active immune responses in synovial tissues and systemic compartme....

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Protocol

All animal experiments were conducted in accordance within the policies of the Institutional Animal Care and Use Committee (IACUC) of Janssen R&D.

1. Cryogenic Freezer Mill-based Pulverization Method

  1. At termination of the CIA study, sacrifice mice with 1.5% isoflurane followed by cervical dislocation.
  2. On the day of tissue processing, pre-chill all instruments (spatulas, grinding vials, etc.) on dry ice for a minimum of 10 min. Wear thermal gloves to avoid freeze damage.
  3. Cut hind paws with a scissor at the fur line as depicted in Figure 1A.
  4. Transfer ....

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Results

Here, we show a representative gel image visualization of RNA extracted from front paws of CIA mice in Figure 2A. The 28S rRNA and the 18S rRNA band indicate all samples have sufficient amount of intact RNA. Next, we show a representative scatter plot of total protein concentrations based on protein BCA analysis in Figure 2B. Total protein concentrations from naïve mice, CIA mice or CIA mice unde.......

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Discussion

Although there is strong scientific rationale to evaluate molecular pathways in synovial tissues, many reports on immune profiling of murine CIA model were focused on peripheral blood, while protein and RNA analysis data of inflamed paws are rather limited. There are several possible reasons for this bias: murine ankle joints are no larger than ~2 cm; the affected areas consist of skin, bone and connective tissues which are often difficult to homogenize using traditional methods like tissue grinders, pestle and mortar, s.......

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Disclosures

The authors BJ, SH, ML, RM, ML, TO and FS are employees of Janssen Research & Development Inc and are shareholders in the parent company, Johnson & Johnson, Inc.

Acknowledgements

The authors wish to thank Edith Janssen for the critical review of the manuscript and Navin Rao and Jennifer Towne for their support of the publication of this manuscript.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
5 mm stainless steel beadQiagen69989
beta-mercaptoethanolSigmaM6250Sample reducing agent that inhibits RNASE enzymes
Bioanalyzer KitAgilent5067-1511RNA qualification kit
b-mercaptoethanolSigmaM6250
Cell Culture Grade WaterCorning25-055-CIWater
Cell lysis stock solutionCell Signaling9803
Eppendorf TubeEppendorf22363204Microfuge tubes
Eppendorf tube centrifuge boxNalgene5055Box for holding eppendorf tubes in horizontal tube arrangement
Everlast 247 Variable Speed RockerBenchmark ScientificBR5000
Freezer MillSpex Sample Prep6875Freezer/Mill for processing paws into pulverized powder
Grinding VialSpex Sample Prep6801Polycarbonate vial for processing paws into pulverized powder
Pierce BCA kitPierce23225Kit for Total Protein Quantification
Protease Inhibitor Cocktail set 1Calbiochem539131Protease Inhibitors
Protein BCA KitPierce23225
Quantigene KitThermofisherQP1013bDNA analysis Kit
Refrigerated microcentrifugeEppendorf5417RCentrifugation
RLT BufferQiagen79216RNA extraction buffer
RNeasy mini kitQiagen74104including RNeasy column, RLT Buffer and RW1 Buffer
ShakerBenchmark ScientificBR5000Rocker/Shaker
SpatulaVWR10806-412Spatula for powder transfer
Stainless Steel BeadQiagen69989Bead for mixing during protein extraction
Tube ExtractorSpex Sample Prep6884Extractor for removing the top of grinding vial
VortexerVWR10153-838Sample mixing

References

  1. Firestein, G. S. Immunologic mechanisms in the pathogenesis of rheumatoid arthritis. Journal of Clinical Rheumatology. 11, S39-S44 (2005).
  2. McInnes, I. B., Schett, G. The pathogenesis of rheumatoid arthritis. New England Journal of Medicine. 365

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