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

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 compartments. The susceptibility of different mouse strains to CIA model links to Major Histocompatibility Complex (MHC) haplotype and antigen specific T cell and B cell interactions^3,4. In addition, many pathogenic pathways in human RA, including autoantibody production, immune complex deposition, myeloid cell activation, polyarticular manifestations and pannus formation with synovial immune infiltration, are also evident in this model^5,6. Investigators have employed this well-established CIA model to investigate effects of anti-inflammatory cytokine treatments⁷. Many biologics approved for autoimmune or inflammatory diseases, such as anti-TNFα and anti-IL-6, are found to be efficacious in the CIA model^8,9.

Profiling the interactions of the immune system in synovial tissue is crucial to elucidate molecular mechanisms associated with the pathogenesis of RA. In the human clinical setting, a common practice is to perform needle synovial biopsies under the guidance of ultrasound imaging. In the preclinical settings, the smaller architecture of the murine joints makes biopsy procedures much more difficult if not impossible. Recently, we demonstrated the utilization of the murine CIA model to evaluate combinations of drugs to impact disparate end-points and resolve disease in a combinatorial approach¹⁰. A cryogenic freezer mill-based pulverization method was employed to process inflamed murine paws into homogeneous fine powders and established downstream processes to extract RNA and proteins. This method protects RNA and protein from enzymatic and chemical degrative processes and enables us to apply multiple analytical methods to a single homogenized sample source.

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 each paw into one 1.5 mL microcentrifuge tube, snap freeze in liquid nitrogen immediately, and store frozen paws at -80 °C. Do not keep samples frozen for more than one week.
5. Fill freezer mill with liquid nitrogen as shown in Figure 1B and let it equilibrate for at least 10 min.
6. Keep unprocessed sample on dry ice and avoid freeze-thaw cycles.
7. Transfer one hind paw into pre-chilled large polycarbonate grinding vial with a bottom steel plug, insert the pre-chilled steel impactor and close the polycarbonate grinding vial with the pre-chilled top steel plug (Figure 1C).
8. Transfer large polycarbonate grinding vials with the samples into the freezer mill pre-filled with liquid and close the lid with the rubber clasp found at the front of the instrument.
9. Let samples cool in liquid nitrogen for 1 minute.
10. Set the freezer mill to the 1 minute program with 10 cycles per second and press the start button. Wait for the freezer mill to complete its cycle.
    NOTE: The machine makes a drumming sound as the steel impactor moves back and forth. Use ear plugs to avoid hearing loss.
11. Open the lid of the freezer mill, take out the large polycarbonate grinding vial and place it in an extractor as depicted in Figure 1D. Remove the top steel plug by placing downward pressure on the black handle until the steel plug slides out of the polycarbonate tube.
12. Transfer the opened large polycarbonate grinding vial onto dry ice. Remove the steel impactor with pre-chilled forceps.
13. Transfer the frozen powder into pre-chilled 50 mL conical tube.
14. Weight 30-50 mg of frozen powder into a tared frozen 1.5 mL microcentrifuge tube for RNA extraction and 100-200 mg of frozen powder for protein extraction.
    NOTE: The frozen powder should look like white or light pink fine sand as depicted in Figure 1E.
15. Store pulverized samples at -80 °C and proceed to RNA and protein isolations within 24 h.

2. RNA Extraction

1. Add 10 µL of β-mercaptoethanol (β-ME) per 1 mL of RLT buffer.
2. Calculate the volume of RLT Buffer corresponding to a ratio of 23.3 mL/mg of tissue and add the appropriate volume of RLT Buffer with β-ME to the tube with frozen powder. This ratio was empirically determined to be ideal for mouse paws.
3. Vortex the sample at 3,000 RPM for 10 s.
4. Mix well by pipetting up-and-down 10 times vigorously with a 1 mL pipettor.
5. Vortex the sample again at 3,000 RPM for 20 s.
6. Centrifuge the tube at 13,000 x g for 2 min.
7. Transfer 700 µL of the supernatants to a fresh tube and add 700 µL of 70% ethanol.
   NOTE: If <700 µL is in the tube, it is acceptable to proceed, still adding equivalent volume of 70% ethanol.
8. Load 700 µL of the sample onto a RNA purification column.
9. Centrifuge the tube at ≥10,000 x g for 30 s.
10. Discard the flow-through and load the remaining part of the sample to the RNeasy column.
11. Centrifuge the tube at ≥10,000 x g for 30 s.
12. Discard the flow through and wash the column by adding 700 µL of RW1 buffer with centrifugation of ≥10,000 x g for 30 s. If performing option DNASE digestion, 350 µL of RW1 is added prior to DNASE treatment.  And an additional 350 µL of RW1 is added following DNASE treatment.
13. Optional) Perform a DNase digestion step follow manufacturer's instructions.
14. Wash the tube twice by adding 500 µL of RPE buffer followed by centrifugation at ≥10,000 x g for 30 s. Discard flow through each time.
15. Dry the column by centrifugation at ≥10,000 x g for 2 min.
16. Elute RNA by adding 50 µL water with centrifugation at ≥10,000 x g for 2 min. Collect flow through and transfer into a new 1.5 mL tube.
17. Determine the quantity of RNA using the researcher's method of choice and store at -80 °C before further analysis.

3. Protein Extraction

1. Dilute the 10x cell lysis stock solution in 1x cell lysis stock solution using cell culture grade water.
2. Reconstitute the Protease Inhibitor Cocktail Set I with 1 mL of water to make a 100x protease inhibitor stock.
3. Add 100 µL of protease inhibitor to 9.9 mL of 1x Cell lysis to make a 1x final stock solution.
4. Add 4 µL of ice cold 1x Cell Lysis Buffer per mg tissue powder (e.g., 800 µL of lysis buffer to 200 mg of tissue powder).
5. Add one 5 mm stainless steel bead to the tube.
6. Vortex the tube at 3,000 RPM for 60 s. Transfer the tube to wet ice and continue to the next sample.
7. Place all sample tubes in a box and shake the centrifuge box on a rocker at 1,000 RPM, 4 °C for 1 h. 
   NOTE: Researchers may find that placing the box vertical can facilitate better mixing with the bead.
8. Centrifuge the tubes at 10,000 x g and 4 °C for 15 min.
9. Transfer the supernatants into a fresh tube and avoid the fat layer on the top.
10. Determine the total protein concentration. 10 to 30-fold dilutions of protein lysate are ideal for a BCA test.
11. Aliquot the sample into 1.5 mL microcentrifuge tubes and store at -80 °C before further analysis.

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...

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...

Materials

List of materials used in this article

Name	Company	Catalog Number	Comments
5 mm stainless steel bead	Qiagen	69989
beta-mercaptoethanol	Sigma	M6250	Sample reducing agent that inhibits RNASE enzymes
Bioanalyzer Kit	Agilent	5067-1511	RNA qualification kit
b-mercaptoethanol	Sigma	M6250
Cell Culture Grade Water	Corning	25-055-CI	Water
Cell lysis stock solution	Cell Signaling	9803
Eppendorf Tube	Eppendorf	22363204	Microfuge tubes
Eppendorf tube centrifuge box	Nalgene	5055	Box for holding eppendorf tubes in horizontal tube arrangement
Everlast 247 Variable Speed Rocker	Benchmark Scientific	BR5000
Freezer Mill	Spex Sample Prep	6875	Freezer/Mill for processing paws into pulverized powder
Grinding Vial	Spex Sample Prep	6801	Polycarbonate vial for processing paws into pulverized powder
Pierce BCA kit	Pierce	23225	Kit for Total Protein Quantification
Protease Inhibitor Cocktail set 1	Calbiochem	539131	Protease Inhibitors
Protein BCA Kit	Pierce	23225
Quantigene Kit	Thermofisher	QP1013	bDNA analysis Kit
Refrigerated microcentrifuge	Eppendorf	5417R	Centrifugation
RLT Buffer	Qiagen	79216	RNA extraction buffer
RNeasy mini kit	Qiagen	74104	including RNeasy column, RLT Buffer and RW1 Buffer
Shaker	Benchmark Scientific	BR5000	Rocker/Shaker
Spatula	VWR	10806-412	Spatula for powder transfer
Stainless Steel Bead	Qiagen	69989	Bead for mixing during protein extraction
Tube Extractor	Spex Sample Prep	6884	Extractor for removing the top of grinding vial
Vortexer	VWR	10153-838	Sample mixing