Skip to main content
Log in

Progressive renal dysfunction and macrophage infiltration in interstitial fibrosis in an adenine-induced tubulointerstitial nephritis mouse model

  • Original Paper
  • Published:
Histochemistry and Cell Biology Aims and scope Submit manuscript

Abstract

Adenine phosphoribosyltransferase deficiency in mice or an excessive oral intake of adenine leads to the accumulation of 2,8-dihydroxyadenine (DHA) in renal tubules and that causes progressive renal dysfunction accompanied by interstitial fibrosis. However, the precise mechanism responsible for DHA-induced progressive fibrosis is not fully understood. The present study investigates the possible involvement of monocytes/macrophages in the progressive fibrosis induced by feeding adenine to mice. Urinary calculi were deposited in tubules on day 7 after the initiation of adenine feeding. Elevation of the serum creatinine level and loss of body weight were observed in a time-dependent manner, suggesting the development of typical renal dysfunction induced by the adenine feeding. In renal tissue, mRNA expression of MCP-1, MIP-1α, RANTES, IL-1β, CCR2, TGF-β, α-smooth muscle actin (α-SMA) and collagen 1a1 was increased in parallel. Along with the increased expression of these genes, a remarkable infiltration of macrophages into the tubulointerstitial area was observed in a time-dependent manner. In addition, in the tubulointerstitial area, α-SMA positive fibroblasts were increased in parallel with collagen deposition. These results suggest that the excessive consumption of adenine leads to progressive renal dysfunction in mice. We speculate that the accumulation of DHA in tubules might stimulate epithelium to produce MCP-1 and that profibrogenic TGF-β produced by infiltrated macrophages might stimulate interstitial fibroblasts to produce collagen. These results indicate that macrophage infiltration is one of the triggers that initiates interstitial fibroblast activation and collagen deposition followed by renal dysfunction.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

References

  • Abbate M, Zoja C, Remuzzi G (2006) How does proteinuria cause progressive renal damage? J Am Soc Nephrol 17:2974–2984

    Article  PubMed  CAS  Google Scholar 

  • Anders HJ, Vielhauer V, Schlondorff D (2003) Chemokines and chemokine receptors are involved in the resolution or progression of renal disease. Kidney Int 63:401–415

    Article  PubMed  CAS  Google Scholar 

  • de Vries A, Sperling O (1977) Implications of disorders of purine metabolism for the kidney and the urinary tract. Ciba Found Symp 48:179–206

    PubMed  Google Scholar 

  • Ding L, Zhao M, Zou W, Liu Y, Wang H (2004) Mycophenolate mofetil combined with prednisone for diffuse proliferative lupus nephritis: a histopathological study. Lupus 13:113–118

    Article  PubMed  CAS  Google Scholar 

  • Engle SJ, Stockelman MG, Chen J, Boivin G, Yum MN, Davies PM, Ying MY, Sahota A, Simmonds HA, Stambrook PJ, Tischfield JA (1996) Adenine phosphoribosyltransferase-deficient mice develop 2, 8-dihydroxyadenine nephrolithiasis. Proc Natl Acad Sci USA 93:5307–5312

    Article  PubMed  CAS  Google Scholar 

  • Iwano M, Plieth D, Danoff TM, Xue C, Okada H, Neilson EG (2002) Evidence that fibroblasts derive from epithelium during tissue fibrosis. J Clin Invest 110:341–350

    PubMed  CAS  Google Scholar 

  • Kalluri R, Neilson EG (2003) Epithelial-mesenchymal transition and its implications for fibrosis. J Clin Invest 112:1776–1784

    PubMed  CAS  Google Scholar 

  • Kitagawa K, Wada T, Furuichi K, Hashimoto H, Ishiwata Y, Asano M, Takeya M, Kuziel WA, Matsushima K, Mukaida N, Yokoyama H (2004) Blockade of CCR2 ameliorates progressive fibrosis in kidney. Am J Pathol 165:237–246

    PubMed  CAS  Google Scholar 

  • Miyajima A, Chen J, Lawrence C, Ledbetter S, Soslow RA, Stern J, Jha S, Pigato J, Lemer ML, Poppas DP, Vaughan ED, Felsen D (2000) Antibody to transforming growth factor-beta ameliorates tubular apoptosis in unilateral ureteral obstruction. Kidney Int 58:2301–2313

    Article  PubMed  CAS  Google Scholar 

  • Monteclaro FS, Charo IF (1996) The amino-terminal extracellular domain of the MCP-1 receptor, but not the RANTES/MIP-1alpha receptor, confers chemokine selectivity. Evidence for a two-step mechanism for MCP-1 receptor activation. J Biol Chem 271:19084–19092

    Article  PubMed  CAS  Google Scholar 

  • Motomura Y, Khan WI, El-Sharkawy RT, Verma-Gandhu M, Verdu EF, Gauldie J, Collins SM (2006) Induction of a fibrogenic response in mouse colon by overexpression of monocyte chemoattractant protein 1. Gut 55:662–670

    Article  PubMed  CAS  Google Scholar 

  • Myllymaki JM, Honkanen TT, Syrjanen JT, Helin HJ, Rantala IS, Pasternack AI, Mustonen JT (2007) Severity of tubulointerstitial inflammation and prognosis in immunoglobulin A nephropathy. Kidney Int 71:343–348

    Article  PubMed  CAS  Google Scholar 

  • Nath KA (1998) The tubulointerstitium in progressive renal disease. Kidney Int 54:992–994

    Article  PubMed  CAS  Google Scholar 

  • Nikolic-Paterson DJ, Atkins RC (2001) The role of macrophages in glomerulonephritis. Nephrol Dial Transplant 16(Suppl 5):3–7

    PubMed  CAS  Google Scholar 

  • Okada H, Kalluri R (2005) Cellular and molecular pathways that lead to progression and regression of renal fibrogenesis. Curr Mol Med 5:467–474

    Article  PubMed  CAS  Google Scholar 

  • Rodriguez-Iturbe B, Pons H, Herrera-Acosta J, Johnson RJ (2001) Role of immunocompetent cells in nonimmune renal diseases. Kidney Int 59:1626–1640

    Article  PubMed  CAS  Google Scholar 

  • Sean Eardley K, Cockwell P (2005) Macrophages and progressive tubulointerstitial disease. Kidney Int 68:437–455

    Article  PubMed  Google Scholar 

  • Segerer S, Nelson PJ, Schlondorff D (2000) Chemokines, chemokine receptors, and renal disease: from basic science to pathophysiologic and therapeutic studies. J Am Soc Nephrol 11:152–176

    PubMed  CAS  Google Scholar 

  • Stockelman MG, Lorenz JN, Smith FN, Boivin GP, Sahota A, Tischfield JA, Stambrook PJ (1998) Chronic renal failure in a mouse model of human adenine phosphoribosyltransferase deficiency. Am J Physiol 275:F154–F163

    PubMed  CAS  Google Scholar 

  • Vielhauer V, Anders HJ, Mack M, Cihak J, Strutz F, Stangassinger M, Luckow B, Grone HJ, Schlondorff D (2001) Obstructive nephropathy in the mouse: progressive fibrosis correlates with tubulointerstitial chemokine expression and accumulation of CC chemokine receptor 2- and 5-positive leukocytes. J Am Soc Nephrol 12:1173–1187

    PubMed  CAS  Google Scholar 

  • Wada T, Yokoyama H, Furuichi K, Kobayashi KI, Harada K, Naruto M, Su SB, Akiyama M, Mukaida N, Matsushima K (1996) Intervention of crescentic glomerulonephritis by antibodies to monocyte chemotactic and activating factor (MCAF/MCP-1). FASEB J 10:1418–1425

    PubMed  CAS  Google Scholar 

  • Wada T, Furuichi K, Sakai N, Iwata Y, Yoshimoto K, Shimizu M, Takeda SI, Takasawa K, Yoshimura M, Kida H, Kobayashi KI, Mukaida N, Naito T, Matsushima K, Yokoyama H (2000) Up-regulation of monocyte chemoattractant protein-1 in tubulointerstitial lesions of human diabetic nephropathy. Kidney Int 58:1492–1499

    Article  PubMed  CAS  Google Scholar 

  • Wada T, Furuichi K, Sakai N, Iwata Y, Kitagawa K, Ishida Y, Kondo T, Hashimoto H, Ishiwata Y, Mukaida N, Tomosugi N, Matsushima K, Egashira K, Yokoyama H (2004) Gene therapy via blockade of monocyte chemoattractant protein-1 for renal fibrosis. J Am Soc Nephrol 15:940–948

    Article  PubMed  CAS  Google Scholar 

  • Yamagami S, Tanaka H, Endo N (1997) Monocyte chemoattractant protein-2 can exert its effects through the MCP-1 receptor (CC CKR2B). FEBS Lett 400:329–332

    Article  PubMed  CAS  Google Scholar 

  • Yokoyama H, Wada T, Furuichi K, Segawa C, Shimizu M, Kobayashi K, Su S, Mukaida N, Matsushima K (1998) Urinary levels of chemokines (MCAF/MCP-1, IL-8) reflect distinct disease activities and phases of human IgA nephropathy. J Leukoc Biol 63:493–499

    PubMed  CAS  Google Scholar 

  • Yokozawa T, Oura H, Koizumi F (1985) 2, 8-Dihydroxyadenine urolithiasis induced by dietary adenine in rats. Nippon Jinzo Gakkai Shi 27:371–378

    PubMed  CAS  Google Scholar 

  • Yokozawa T, Zheng PD, Oura H, Koizumi F (1986) Animal model of adenine-induced chronic renal failure in rats. Nephron 44:230–234

    Article  PubMed  CAS  Google Scholar 

Download references

Acknowledgments

We thank Mr. Y. Nakayama (Teijin Pharma Limited) for his excellent technical assistance and Prof. A.M. Bari (Department of Pathology, Bangladesh Agricultural University) for critical reading of this manuscript. This work was supported in part by a Grant-in-Aid for Scientific Research from the Japanese Ministry of Education, Culture, Sports, Science and Technology.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Hiroshi Ozaki.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Tamura, M., Aizawa, R., Hori, M. et al. Progressive renal dysfunction and macrophage infiltration in interstitial fibrosis in an adenine-induced tubulointerstitial nephritis mouse model. Histochem Cell Biol 131, 483–490 (2009). https://doi.org/10.1007/s00418-009-0557-5

Download citation

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00418-009-0557-5

Keywords

Navigation