Distinct Expression of CCR1 and CCR5 in Glomerular and Interstitial Lesions of Human Glomerular Diseases

• Published in: American journal of nephrology Vol. 20; no. 4; pp. 291 - 299
• Main Authors: Furuichi, Kengo, Wada, Takashi, Sakai, Norihiko, Iwata, Yasunori, Yoshimoto, Keiichi, Shimizu, Miho, Kobayashi, Ken-ichi, Takasawa, Kazuya, Kida, Hiroshi, Takeda, Shin-ichi, Mukaida, Naofumi, Matsushima, Kouji, Yokoyama, Hitoshi
• Format: Journal Article
• Language: English
• Published: Basel, Switzerland Karger 01.07.2000; S. Karger AG
• Subjects: Adolescent; Adult; Aged; Aged, 80 and over; Biological and medical sciences; Chemokine CCL3; Chemokine CCL4; Chemokine CCL5 - physiology; Clinical Study; Female; Glomerulonephritis; Glucocorticoids - therapeutic use; Humans; Immunohistochemistry; Kidney Diseases - drug therapy; Kidney Diseases - metabolism; Kidney Diseases - pathology; Kidney Glomerulus - drug effects; Kidney Glomerulus - metabolism; Kidney Glomerulus - pathology; Lupus Nephritis - metabolism; Macrophage Inflammatory Proteins - physiology; Macrophages - metabolism; Male; Medical sciences; Middle Aged; Nephrology. Urinary tract diseases; Nephropathies. Renovascular diseases. Renal failure; Receptors, CCR1; Receptors, CCR5 - metabolism; Receptors, Chemokine - metabolism; T-Lymphocytes - metabolism; CCR1; CCR5; RANTES; Chemokines; MIP-1α; Kidney disease; Human; Immunohistochemistry; Glomerulonephritis; Pathology; Urinary system disease; Exploration; Diagnosis; Kidney
• ISSN: 0250-8095; 1421-9670
• DOI: 10.1159/000013603

We investigated the presence of CCR1- and CCR5-positive cells immunohistochemically in the kidneys of 38 patients with several renal diseases, including 13 crescentic glomerulonephritis patients. In addition, we determined cell phenotypes of CCR1- and CCR5-positive cells using a dual immunostaining technique. Urinary levels of their ligands, for CCR1 and CCR5; macrophage inflammatory protein (MIP)-1α, MIP-1β and regulated upon activation in normal T cells expressed and secreted (RANTES) were evaluated by enzyme-linked immunosorbent assay. CCR1- and CCR5-positive cells were detected in both glomeruli and interstitium of the diseased kidneys. Using a dual immunostaining technique, these positive cells were CD68-positive macrophages (MΦ) and CD3-positive T cells. The number of CCR1-positive cells in glomeruli was correlated with urinary levels of MIP-1α. The number of CCR1-positive cells in the interstitium was correlated with both urinary MIP-1α and RANTES levels. CCR1-positive cells in the interstitium remained after glucocorticoid therapy, most of which were MΦ, and were correlated with the intensity of interstitial fibrosis and tubular atrophy. Glomerular CCR5-positive cells were well correlated with extracapillary lesions and urinary MIP-1α levels, while interstitial CCR5-positive cells, mainly CD3-positive T cells, were correlated with interstitial lesions and urinary RANTES levels. Renal CCR5-positive cells were dramatically decreased during convalescence induced by glucocorticoids. These results suggest that chemokine receptor signaling may be pivotal for human renal diseases through the recruitment and activation of MΦ and T cells; CCR5-positive cells may participate in glomerular lesions including extracapillary lesions via MIP-1α and in interstitial lesions via RANTES. CCR1 may be involved in interstitial lesions in resolving phase after glucocorticoid therapy.