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This Article Full Text Full Text (PDF) All Versions of this Article: 292/2/F749    most recent 00034.2006v1 Alert me when this article is cited Alert me if a correction is posted Citation Map Services Email this article to a friend Similar articles in this journal Similar articles in ISI Web of Science Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Kishore, B. K. Articles by Westenfelder, C. Search for Related Content PubMed PubMed Citation Articles by Kishore, B. K. Articles by Westenfelder, C.

Administration of poly-D-glutamic acid induces proliferation of erythropoietin-producing peritubular cells in rat kidney

Departments of ¹Internal Medicine, ²Physiology, and ⁴Pathology, University of Utah Health Sciences Center, ⁵Associated Regional University Pathologists Laboratories, and ³Nephrology Research, Veterans Affairs Salt Lake City Health Care System, Salt Lake City, Utah

Submitted 30 January 2006 ; accepted in final form 28 September 2006

Erythropoietin (EPO), a 34-kDa glycoprotein, is produced predominantly by peritubular interstitial cells (PIC) in the renal cortex and is physiologically released when ambient oxygen pressure falls. However, the exact nature of EPO-producing cells in the kidney is not well understood. We discovered that brief administration of a low-molecular-weight synthetic peptide, poly-D-glutamic acid (PDG), induced prompt and robust expansion of EPO-producing PIC in rat kidney, without evidence of tubular cell necrosis/apoptosis or fibrotic reaction. Proliferating PIC in PDG-treated rats were noninflammatory, -smooth muscle actin negative, and specifically expressed CD73 (ecto-5'-nucleotidase), EPO mRNA, and protein. Increased numbers of EPO-positive PIC persisted even after the cessation of PDG treatment. No erythropoietic effects of EPO were detected, potentially suggesting maintained physiological control of EPO secretion in this normoxic model. We showed previously that PDG is readily filtered and is rapidly taken up and stored in lysosomes of proximal tubular cells (PTC), resulting in an apparently nonnoxious lysosomal storage condition by virtue of its nonhydrolyzable nature (Kishore BK, Maldague P, Tulkens PM, Courtoy PJ. Lab Invest 74: 1013–1023, 1996). Based on these findings, we suggest that unknown signaling molecules, produced by PTC in response to lysosomal PDG storage, appear to specifically stimulate the proliferation of EPO-producing PIC. We conclude that this model is uniquely suited to investigate the biology of EPO production by PIC and may thus facilitate the development of novel and more economical therapies of anemias and other EPO-responsive conditions.

anemia; proximal tubular cell; fibroblasts; immunohistochemistry; in situ hybridization