Ex vivo programmed macrophages ameliorate experimental chronic inflammatory renal disease

• Published in: Kidney international Vol. 72; no. 3; pp. 290 - 299
• Main Authors: Wang, Y., Wang, Y.P., Zheng, G., Lee, V.W.S., Ouyang, L., Chang, D.H.H., Mahajan, D., Coombs, J., Wang, Y.M., Alexander, S.I., Harris, D.C.H.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01-08-2007; Elsevier Limited
• Subjects: Adoptive Transfer - methods; Animals; Cell Movement - physiology; cell transfer; Cells, Cultured; Chemokine CCL17; Chemokines, CC - metabolism; chronic renal disease; Disease Models, Animal; Down-Regulation; Doxorubicin; Glomerulosclerosis, Focal Segmental - chemically induced; Glomerulosclerosis, Focal Segmental - immunology; Glomerulosclerosis, Focal Segmental - prevention & control; Interleukin-10 - metabolism; Interleukin-13 - pharmacology; Interleukin-4 - pharmacology; Lipopolysaccharides - pharmacology; Macrophage Activation; macrophages; Macrophages - drug effects; Macrophages - physiology; Macrophages - transplantation; Male; Mice; Mice, Inbred BALB C; Mice, SCID; Nitric Oxide Synthase Type II - metabolism; Phenotype; Tumor Necrosis Factor-alpha - metabolism; macrophages; cell transfer; chronic renal disease
• ISSN: 0085-2538; 1523-1755
• DOI: 10.1038/sj.ki.5002275

Macrophage infiltration of the kidney is a prominent feature associated with the severity of renal injury and progressive renal failure. To determine the influence of macrophages in renal disease models in the absence of endogenous T and B cells, we performed adoptive transfer of macrophages into severe combined immunodeficient (SCID) mice. In this study, macrophages were isolated from the spleens of BALB/c mice and stimulated with lipopolysaccharide to induce classically activated M1 macrophages or with interleukin-4 (IL-4) and IL-13 to induce alternatively activated M2 macrophages. These macrophages were then infused into SCID mice with adriamycin nephropathy; an in vivo model of chronic inflammatory renal disease analogous to human focal segmental glomerulosclerosis. Mice infused with M1 macrophages had a more severe histological and functional injury, whereas M2 macrophage-induced transfused mice had reduced histological and functional injury. Both M1 and M2 macrophages localized preferentially to the area of injury and maintained their phenotypes even after 4 weeks. The protective effect of M2 macrophages was associated with reduced accumulation and possibly downregulated chemokine and inflammatory cytokine expression of the host infiltrating macrophages. Our findings demonstrate that macrophages not only act as effectors of immune injury but can be induced to provide protection against immune injury.