Nephrocan, a novel member of the small leucine-rich repeat protein family, is an inhibitor of transforming growth factor-β signaling

被引:26
作者
Mochida, Yoshiyuki
Parisuthiman, Duenpim
Kaku, Masaru
Hanai, Jun-ichi
Sukhatme, Vikas P.
Yamauchi, Mitsuo
机构
[1] Univ N Carolina, Dent Res Ctr, Chapel Hill, NC 27599 USA
[2] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Ctr Study Tumor Microenvironm,Div Nephrol, Boston, MA 02215 USA
[3] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Ctr Study Tumor Microenvironm,Div Hematol Oncol, Boston, MA 02215 USA
[4] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Ctr Study Tumor Microenvironm,Dept Med, Boston, MA 02215 USA
[5] Harvard Univ, Sch Med, Beth Israel Deaconess Med Ctr, Ctr Study Tumor Microenvironm,Dept Pathol, Boston, MA 02215 USA
关键词
D O I
10.1074/jbc.M604787200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In a search of new, small leucine-rich repeat proteoglycan/protein (SLRP) family members, a novel gene, nephrocan (NPN), has been identified. The gene consists of three exons, and based on the deduced amino acid sequence, NPN has 17 leucine-rich repeat motifs and unique cysteine-rich clusters both in the N and C termini, indicating that this gene belongs to a new class of SLRP family. NPN mRNA was predominantly expressed in kidney in adult mice, and during mouse embryogenesis, the expression was markedly increased in 11-day-old embryos at a time when early kidney development takes place. In the adult mouse kidney, NPN protein was located in distal tubules and collecting ducts. When NPN was overexpressed in cell culture, the protein was detected in the cultured medium, and upon treatment with N-glycosidase F, the molecular mass was lowered by similar to 14 kDa, indicating that NPN is a secreted N-glycosylated protein. Furthermore, transforming growth factor-beta(TGF-beta)-responsive 3TP promoter luciferase activity was down-regulated, and TGF-beta-induced Smad3 phosphorylation was also inhibited by NPN, suggesting that NPN suppresses TGF-beta/Smad signaling. Taken together, NPN is a novel member of the SLRP family that may play important roles in kidney development and pathophysiology by functioning as an endogenous inhibitor of TGF-beta signaling.
引用
收藏
页码:36044 / 36051
页数:8
相关论文
共 51 条
[1]   Expression of lysyl oxidase isoforms in MC3T3-El osteoblastic cells [J].
Atsawasuwan, P ;
Mochida, Y ;
Parisuthiman, D ;
Yamauchi, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 327 (04) :1042-1046
[2]   A ureteric bud cell line induces nephrogenesis in two steps by two distinct signals [J].
Barasch, J ;
Pressler, L ;
Connor, J ;
Malik, A .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL FLUID AND ELECTROLYTE PHYSIOLOGY, 1996, 271 (01) :F50-F61
[3]   Genes and proteins involved in mesenchymal to epithelial transition [J].
Barasch, J .
CURRENT OPINION IN NEPHROLOGY AND HYPERTENSION, 2001, 10 (03) :429-436
[4]   Mesenchymal to epithelial conversion in rat metanephros is induced by LIF [J].
Barasch, J ;
Yang, J ;
Ware, CB ;
Taga, T ;
Yoshida, K ;
Erdjument-Bromage, H ;
Tempst, P ;
Parravicini, E ;
Malach, S ;
Aranoff, T ;
Oliver, JA .
CELL, 1999, 99 (04) :377-386
[5]   Leucine-rich repeats and pathogen recognition in Toll-like receptors [J].
Bell, JK ;
Mullen, GED ;
Leifer, CA ;
Mazzoni, A ;
Davies, DR ;
Segal, DM .
TRENDS IN IMMUNOLOGY, 2003, 24 (10) :528-533
[6]   NATURAL INHIBITOR OF TRANSFORMING GROWTH-FACTOR-BETA PROTECTS AGAINST SCARRING IN EXPERIMENTAL KIDNEY-DISEASE [J].
BORDER, WA ;
NOBLE, NA ;
YAMAMOTO, T ;
HARPER, JR ;
YAMAGUCHI, Y ;
PIERSCHBACHER, MD ;
RUOSLAHTI, E .
NATURE, 1992, 360 (6402) :361-364
[7]  
BORDER WA, 1994, NEW ENGL J MED, V331, P1286
[8]   The small leucine-rich proteoglycan biglycan modulates BMP-4-induced osteoblast differentiation [J].
Chen, XD ;
Fisher, LW ;
Robey, PG ;
Young, MF .
FASEB JOURNAL, 2004, 18 (09) :948-958
[9]   Unusual molecular architecture of the Yersinia pestis cytotoxin YopM:: A leucine-rich repeat protein with the shortest repeating unit [J].
Evdokimov, AG ;
Anderson, DE ;
Routzahn, KM ;
Waugh, DS .
JOURNAL OF MOLECULAR BIOLOGY, 2001, 312 (04) :807-821
[10]   INTERACTION OF THE SMALL INTERSTITIAL PROTEOGLYCANS BIGLYCAN, DECORIN AND FIBROMODULIN WITH TRANSFORMING GROWTH-FACTOR-BETA [J].
HILDEBRAND, A ;
ROMARIS, M ;
RASMUSSEN, LM ;
HEINEGARD, D ;
TWARDZIK, DR ;
BORDER, WA ;
RUOSLAHTI, E .
BIOCHEMICAL JOURNAL, 1994, 302 :527-534