Sep 16, 2020
Version 1
Immunohistochemical staining of CD44 core proteins in islet beta cells of formalin-fixed mouse pancreas V.1
- Lora Starrs1,
- Debra Brown1,
- Sarah Popp1,
- Charmaine Simeonovic1
- 1The Australian National University
External link: https://doi.org/10.1371/journal.pone.0252607
Protocol Citation: Lora Starrs, Debra Brown, Sarah Popp, Charmaine Simeonovic 2020. Immunohistochemical staining of CD44 core proteins in islet beta cells of formalin-fixed mouse pancreas. protocols.io https://dx.doi.org/10.17504/protocols.io.bmgfk3tn
Manuscript citation:
Dhounchak S, Popp SK, Brown DJ, Laybutt DR, Biden TJ, Bornstein SR, Parish CR, Simeonovic CJ (2021) Heparan sulfate proteoglycans in beta cells provide a critical link between endoplasmic reticulum stress, oxidative stress and type 2 diabetes. PLoS ONE 16(6): e0252607. doi: 10.1371/journal.pone.0252607
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: September 16, 2020
Last Modified: September 16, 2020
Protocol Integer ID: 42215
Keywords: CD44, Immunohistochemistry, Mouse pancreas
Abstract
Paraffin sections (4mm thickness) of formalin-fixed mouse pancreases were treated with heat/citrate buffer for antigen retrieval. CD44 core proteins were detected immunohistochemically using rat anti-mouse CD44 mAb (IM7 mAb; BD Biosciences) or mouse anti-human CD44v3 mAb (CD44v3: R&D Systems), with horseradish peroxidase-conjugated rabbit anti-rat Ig (Dako) or rabbit anti-mouse Ig (Dako). Background staining was checked using the corresponding isotype control Ig instead of the primary antibody. 3-amino-9-ethylcarbazole (AEC) was used as the chromogen. For morphometry, stained sections were imaged using a light microscope with attached camera (Olympus BX41). Image J software with color deconvolution plugin was used for the quantitative analysis of the % of islet area stained.
Guidelines
Rat anti-mouse CD44 (IM7) mAb recognises all CD44 isoforms (1-4)and mouse anti-human CD44v3 mAb recognises a CD44 isoform that carries HS side-chains (1-3). In mouse pancreas we have demonstrated that these two mAbs have a similar pattern of intra-islet staining.
References:
1. Bennett KL, Jackson DG, Simon JC, Tanczos E, Peach R, Modrell B, et al. CD44 isoforms containing exon V3 are responsible for the presentation of heparin-binding growth factor. The Journal of cell biology. 1995;128(4):687-98.
2. Jackson DG, Bell JI, Dickinson R, Timans J, Shields J, Whittle N. Proteoglycan forms of the lymphocyte homing receptor CD44 are alternatively spliced variants containing the v3 exon. The Journal of cell biology. 1995;128(4):673-85.
3. Martegani MP, Del Prete F, Gasbarri A, Natali PG, Bartolazzi A. Structural variability of CD44v molecules and reliability of immunodetection of CD44 isoforms using mAbs specific for CD44 variant exon products. Am J Pathol. 1999;154(1):291-300.
4. Rops AL, van der Vlag J, Lensen JF, Wijnhoven TJ, van den Heuvel LP, van Kuppevelt TH, et al. Heparan sulfate proteoglycans in glomerular inflammation. Kidney international. 2004;65(3):768-85.
Before start
Materials:
1. Prepare graded alcohols and xylene for deparaffinizing tissue sections: 2 x xylene (250 ml/slide container), 2 x absolute ethanol (250 ml/slide container), 1 x 90% ethanol (250 ml), 1 x 70% ethanol (250 ml).
2. Prepare acetate buffer components:
(i) 0.1N acetic acid: 290 ml glacial acetic acid in 50 ml deionized water
(ii) 0.1M sodium acetate: 410 mg anhydrous CH3COONa in 50 ml deionized water.
Prepare 0.1M acetate buffer (pH 5.2) by mixing 10.5 ml 0.1N acetic acid and 39.5 ml 0.1M sodium acetate.
3. Prepare stock solution of 3-amino-9-ethylcarbazole (AEC; chromogen, 8 mg/ml: 40 mg AEC in 5 ml N-N-dimethyl formamide; protect from light and refrigerate at 4ºC.
4. Prepare M.O.M. diluent: 200 ml M.O.M. protein concentrate stock solution (M.O.M immunodetection kit) in 2.5 ml phosphate-buffered saline (PBS) for use either as a blocking step to minimize non-specific Ig binding or for diluting antibodies.
5. Mabs and pAbs:
rat anti-mouse CD44 (IM7) mAb, BD Biosciences #553130 or
mouse anti-human CD44v3 mAb, R&D systems BBA11
horseradish peroxidase (HRP)-conjugated rabbit anti-rat Ig, Dako #PO450 (alternative HRP-rabbit anti-rat IgG, Sigma #A5795)
or HRP-rabbit anti-mouse IgG, Invitrogen #31450 (for use with CD44v3 mAb as primary ab)
Purified NA/LE Rat IgG2bκ , BD Biosciences #555845 or
Purified Mouse IgG2bk, BD Biosciences#557351
6. Other reagents:
Hydrogen peroxide (30% w/w), Chem-Supply Pty Ltd (Australia) #HA154-500M,
Methanol, Merck # CAS-No. 67-56-1
3Amino-9-ethylcarbazole (AEC), Sigma-Aldrich #A5754
Animal free blocker, Vector Labs #SP-5030
Stock protein concentrate, M.O.M immunodetection kit, Vector Labs # PK-2200
N-N-dimethyl formamide, Sigma #D158550
Glycergel mounting medium, Dako #C0563
See Guidelines before starting
Deparaffinize slides in each xylene for 1 min. rehydrate slides in graded alcohols beginning in absolute ethanol (10 dips)/ container of absolute ethanol), followed by 90% ethanol (10 dips) and 70% ethanol (10 dips).Wash well in running tap water for 5 min.
Wipe around sections with a tissue, encircle the sections using a diamond pencil and place in a slide container of tap water (250 ml).
Block endogenous peroxidase activity by incubating sections in 3% hydrogen peroxide in methanol (25 ml 30% H2O2 + 225 ml methanol).
Wash 2 x 2 min in 250 ml phosphate-buffered saline (PBS) followed by wash in running tap water for 5 min.
Prepare citrate buffer, pH 6 for antigen retrieval. Dissolve 1.05 g Citric acid in 500 ml deionized waterand pH using 2 - 10 M NaOH.
Transfer slides to 250ml citrate buffer and heat in microwave (1600 watt) for 2 min on High power followed by 2 x 6 min on Low power.Allow the slides to cool on the bench for 30 min. Wash slides in 250 ml PBS, 3 x 10 min.
Wipe around sections using tissue. To block non-specific binding of Ig, apply animal free block (diluted to 20% v/v with deionized water) to tissue sections and incubate for 10 min at room temperature.
Tip off excess block in Step 7, wipe around sections using tissue and incubate with 40 μg/ml anti-CD44 (IM7) mAb (or 40 μg/ml rat IgG2bκ as isotype control; diluted in M.O.M. diluent), 125-150 μl/section at room temperature for 1 hour. Alternatively use 10 μg/ml mouse anti-human CD44v3 mAb (or 10 μg/ml mouse IgG2bκas isotype control Ig)
Wash off primary antibody with PBS and transfer slides to slide container with 250 ml PBS. Wash 2 x 2min.
Wipe around sections using tissue and incubate with 52 μg/ml secondary HRP-rabbit anti-mouse Ig (Dako; or alternative 30-60 μg/ml, Sigma) , 150 μl/section, for 30 min at room temperature.
Wash off secondary antibody with PBS and transfer to slide container with 250 ml PBS. Wash slides 2 x 2min.
Prepare AEC working solution: 4.75 ml acetate buffer (see Guidelines), 0.25ml AEC stock solution and 25 μl 3% H2O2. Filter using a disposable 0.2 μm filter. Use within 2 hours of preparation, refrigerate for short-term storage. Protect from light.
Wipe around sections using tissue and cover the sections with AEC solution for 30 min at room temperature.
Wash off AEC solution with deionized water and transfer slides to slide container with 250 ml deionized water. Wash 3x in 10 min.
Lightly counterstain with Gill’s hematoxylin, wash in deionized water (2 x) and briefly dip in ammonium water (100 μl ammonia in 250 ml deionized water), 2 x 2 sec. Wash in deionized water (2x in 250 ml) and coverslip using glycergel mounting medium.
Image sections using a light microscope with camera attachment. Use Image J software with color deconvolution plugin to determine % of islet area stained.