“…18 To stain MPOpositive cells, fixed whole mounts were incubated for 10 min in a 1 : 10 dilution of 10 mL KRB, containing 10 mg Hanker-Yatesreagent (Polysciences, Warrington, PA, USA) and 100 ll hydrogen peroxide. 20 Mast cells were stained by overnight incubation with fluorescein isothiocyanate-avidin (1 : 10 in 10% normal horse serum) at 4°C followed by washouts in PBT. 4 Staining of macrophages was performed by preincubation in 5% normal donkey serum, followed by incubation with the primary antibody (ED2, mouse antirat CD 163; Abd Serotec, D€ usseldorf, Germany; 1 : 100 in PBT with 2.5% NDS), washouts in PBT, and incubation with the secondary antibody (donkey antimouse; Millipore, Temecula, CA, USA; 1 : 500 in PBT).…”