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2 protocols using 70r cr008

1

Intervertebral Disc Histological Analyses

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Caudal spines from 8 and 14-month old WT and MCT4 KO mice were harvested and fixed in 4% PFA for 24 hours and decalcified in 12.5% EDTA at 4oC for 15 days prior to paraffin embedding. Mid-coronal IVD sections (Ca5–8) were stained with Safranin O/Fast Green/Hematoxylin or Picrosirius red, then visualized using a light microscope (AxioImager 2, Carl Zeiss) or a polarizing microscope (Eclipse LV100 POL, Nikon). Histopathological scores were collected from n = 4 mice/genotype with 3 discs per mouse (total 12 discs/genotype) at 8 months; n = 8 mice/genotype with 3 discs per mouse (total 24 discs/genotype) at 14 months. Modified Thompson Grading was used to score NP and AF compartments (Table S2) and Boos Grading Scale was used to score the CEP compartment (5 (link),36 (link)). Histological sections were incubated with antibody against KRT19 (1:3, DSHB, TROMA-III/supernatant), CA3 (1:150, Santa Cruz, sc-50715), MMP13 (1:200, Abcam, ab39012), Aggrecan (1:50, Millipore, AB1031), Collagen I (1:100, Abcam, ab34710), Collagen II (1:400, Fitzgerald, 70R-CR008), Collagen X (1:500, Abcam, ab58632), LDHA (1:200, Novus, NBP2–19320), CA9 (1:200, Novus, NB100–417), MCT1 (1:200, Santa Cruz), GLUT-1 (1:200, Abcam, ab40084) and ARGxx (1:200, Abcam, ab3773). See Supplemental Methods.
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2

Immunohistochemical Analysis of Extracellular Matrix

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De‐paraffinized sections following antigen retrieval were blocked in 5% normal serum in PBS‐T and incubated with antibodies against collagen I (1:100, Abcam ab34710), collagen II (1:400, Fitzgerald 70R‐CR008), collagen X (1:500, Abcam ab58632), aggrecan (1:50, Millipore AB1031); chondroitin sulphate (1:300, Abcam ab11570); CA3 (1:150, SantaCruz), Ki67 (1:100, Abcam ab15580) and p21 (1:200, Novus NB100‐1941). For GLUT‐1 (1:200, Abcam, ab40084) and ARGxx (1:200, Abcam, ab3773) staining, MOM kit (Vector laboratories, BMK‐2202) was used for blocking and primary antibody incubation. Tissue sections were washed and incubated with Alexa Fluor‐594‐conjugated secondary antibody (Jackson ImmunoResearch Lab, Inc., 1:700). The sections were mounted with ProLong® Gold Antifade Mountant with DAPI (Fisher Scientific, P36934) and visualized with Axio Imager 2 microscope using 5×/0.15 N‐Achroplan or 20×/0.5 EC Plan‐Neofluar objectives (Carl Zeiss). Staining area and cell number quantification was performed using the ImageJ software. Images were thresholder to subtract the background, transformed into binary, and then staining area and cell number were calculated using the analyse particles function.
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