Increased Density of Interstitial Mast Cells in Amyloid A Renal Amyloidosis

• Published in: Modern pathology 2000-09, Vol.13 (9), p.1020-1028
• Main Authors: Tóth, Tibor, Tóth-Jakatics, Ria, Jimi, Shiro, Takebayashi, Shigeo
• Format: Article
• Language: English
• Subjects: Actins - metabolism; Amyloid; Amyloidosis; Amyloidosis - metabolism; Amyloidosis - pathology; Antigens, CD - metabolism; Basic fibroblast growth factor; Biomarkers - analysis; Biopsy; Cell Count; Chymases; Creatinine - blood; Female; Fibroblast Growth Factor 2 - immunology; Fibroblast Growth Factor 2 - metabolism; Fibroblasts; Fibrosis; Growth factors; Humans; Immunoenzyme Techniques; Integrin; Integrin beta1 - immunology; Integrin beta1 - metabolism; Kidney; Kidney - metabolism; Kidney - pathology; Kidney diseases; Laboratory Medicine; Male; Mast cell; Mast Cells - classification; Mast Cells - metabolism; Mast Cells - pathology; Medicine; Medicine & Public Health; Middle Aged; Myofibroblasts; Nephritis, Interstitial - metabolism; Nephritis, Interstitial - pathology; original-article; Pathology; Serine Endopeptidases - immunology; Serine Endopeptidases - metabolism; Serum Amyloid A Protein - metabolism; Tryptases
• ISSN: 0893-3952; 1530-0285
• DOI: 10.1038/modpathol.3880184

Renal interstitial fibrosis is the final common pathway leading to end-stage renal disease in various nephropathies including renal amyloidosis. However, the role of mast cells (MCs) in the fibrotic process of renal amyloidosis is not fully understood. We compared the distribution of MCs in renal biopsies from 30 patients with AA type renal amyloidosis and 20 control cases. Immunoreactivity of renal MCs to anti-tryptase and anti-chymase was studied. Interstitial myofibroblasts were stained with anti-α-smooth muscle actin (α-SMA) antibody, and inflammatory cells were identified by anti-CD45, -CD20, and -CD68 mAbs. Positively stained cells were counted, and the relative interstitial and fractional areas of anti-α-SMA stained cells were measured. Anti-CD29 mAb was used to detect β1 integrin and anti-basic fibroblast growth factor (bFGF) mAb for the growth factor on MCs. MCs were rarely found in control samples. In contrast, samples showing amyloid deposition contained numerous tryptase-positive (MCT) (940.17 ± 5.4 versus 6.74 ± 1.1/mm2) but fewer chymase-positive (MCTC) cells (20.7 ± 2.86 versus 1.7 ± 0.76/mm2) in the renal interstitium. There was a significant relationship between interstitial MCT and creatinine clearance (r = −0.72), and between interstitial MCT and glomerular amyloid-index (GAI) (r = 0.723) and interstitial amyloid area (r = 0.824). Accumulation of MCs correlated significantly with the number of T lymphocytes (MCT: r = 0.694). There was also a significant relationship between mast cell (MC) number and the fractional area of α-SMA positive interstitium (r = 0.733) and interstitial fibrotic area (r = 0.6). Double immunostaining demonstrated intracytoplasmic presence of β1 integrin on 87% of MCT and correlated significantly with the interstitial amyloid area (r = 0.818, P = .001) and T-cell number (r = 0.639, P = .002). bFGF was also detected on 85.5% of MCTC correlating well with the interstitial α-SMA-area (r = 0.789). Our results indicate that MCs constitute an integral part of the overall inflammatory process and play a crucial role in interstitial fibrosis in renal amyloidosis.