Identification of a receptor for Reg (Regenerating gene) protein, a pancreatic β-cell regeneration factor

被引:140
作者
Kobayashi, S
Akiyama, T
Nata, K
Abe, M
Tajima, M
Shervani, NJ
Unno, M
Matsuno, S
Sasaki, H
Takasawa, S
Okamoto, H
机构
[1] Tohoku Univ, Grad Sch Med, Dept Biochem, Aoba Ku, Sendai, Miyagi 9808575, Japan
[2] Tohoku Univ, Grad Sch Med, Dept Surg, Aoba Ku, Sendai, Miyagi 9808575, Japan
[3] Tohoku Univ, Grad Sch Med, Dept Geriatr Med, Aoba Ku, Sendai, Miyagi 9808575, Japan
关键词
D O I
10.1074/jbc.275.15.10723
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
Reg (regenerating gene) was isolated as a gene specifically expressed in regenerating islets (Terazono, K., Yamamoto, H., Takasawa, S., Shiga, K., Yonemura, Y., Tochino, Y., and Okamoto, H. (1988) J. Biol. Chem, 263, 2111-2114), Rat and human Reg gene products, Reg/REG proteins, have been demonstrated to stimulate islet beta-cell growth in vitro and in vivo and to ameliorate experimental diabetes. In the present study, we isolated a cDNA for the Reg protein receptor from a rat islet cDNA library. The cDNA encoded a cell surface 919-amino acid protein, and the cells into which the cDNA had been introduced bound Reg protein with high affinity. When the cDNA was introduced into RINm5F cells, a pancreatic beta-cell line that shows Reg-dependent growth, the transformants exhibited significant increases in the incorporation of 5'-bromo-2'-deoxyuridine as well as in the cell numbers in response to Reg protein. A homology search revealed that the cDNA is a homologue to a human multiple exostoses-like gene, the function of which has hitherto been unknown. These results strongly suggest that the receptor is encoded by the exostoses-like gene and mediates a growth signal of Reg protein for beta-cell regeneration.
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页码:10723 / 10726
页数:4
相关论文
共 44 条
[1]   CLONING OF THE PUTATIVE TUMOR-SUPPRESSOR GENE FOR HEREDITARY MULTIPLE EXOSTOSES (EXT1) [J].
AHN, J ;
JOSEFLUDECKE, H ;
LINDOW, S ;
HORTON, WA ;
LEE, B ;
WAGNER, MJ ;
HORSTHEMKE, B ;
WELLS, DE .
NATURE GENETICS, 1995, 11 (02) :137-143
[2]   Expression of Reg and cytokeratin 20 during ductal cell differentiation and proliferation in a mouse model of autoimmune diabetes [J].
Anastasi, E ;
Ponte, E ;
Gradini, R ;
Bulotta, A ;
Sale, P ;
Tiberti, C ;
Okamoto, H ;
Dotta, F ;
Di Mario, U .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 1999, 141 (06) :644-652
[3]   Reg gene expression is increased in rat gastric enterochromaffin-like cells following water immersion stress [J].
Asahara, M ;
Mushiake, S ;
Shimada, S ;
Fukui, H ;
Kinoshita, YA ;
Kawanami, C ;
Watanabe, T ;
Tanaka, S ;
Ichikawa, A ;
Uchiyama, Y ;
Narushima, Y ;
Takasawa, S ;
Okamoto, H ;
Tohyama, M ;
Chiba, T .
GASTROENTEROLOGY, 1996, 111 (01) :45-55
[4]  
Baeza N, 1996, DIABETES METAB, V22, P229
[5]   Pancreatic regenerating gene overexpression in the nonobese diabetic mouse during active diabetogenesis [J].
Baeza, NJ ;
Moriscot, CI ;
Renaud, WP ;
Okamoto, H ;
Figarella, CG ;
Vialettes, BH .
DIABETES, 1996, 45 (01) :67-70
[6]   Expression of REG protein during cell growth and differentiation of two human colon carcinoma cell lines [J].
Bernard-Perrone, FR ;
Renaud, WP ;
Guy-Crotte, OM ;
Bernard, P ;
Figarella, CG ;
Okamoto, H ;
Balas, DC ;
Senegas-Balas, FO .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1999, 47 (07) :863-870
[7]   HIP/PAP is an adhesive protein expressed in hepatocarcinoma, normal Paneth, and pancreatic cells [J].
Christa, L ;
Carnot, F ;
Simon, MT ;
Levavasseur, F ;
Stinnakre, MG ;
Lasserre, C ;
Thepot, D ;
Clement, B ;
Devinoy, E ;
Brechot, C .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 1996, 271 (06) :G993-G1002
[8]   Regenerating gene protein may mediate gastric mucosal proliferation induced by hypergastrinemia in rats [J].
Fukui, H ;
Kinoshita, Y ;
Maekawa, T ;
Okada, A ;
Waki, S ;
Hassan, S ;
Okamoto, H ;
Chiba, T .
GASTROENTEROLOGY, 1998, 115 (06) :1483-1493
[9]   CLONING OF A CDNA-ENCODING RAT BONE-MARROW STROMAL CELL ANTIGEN-1 (BST-1) FROM THE ISLETS OF LANGERHANS [J].
FURUYA, Y ;
TAKASAWA, S ;
YONEKURA, H ;
TANAKA, T ;
TAKAHARA, J ;
OKAMOTO, H .
GENE, 1995, 165 (02) :329-330
[10]   IDENTIFICATION OF PROGRAMMED CELL-DEATH INSITU VIA SPECIFIC LABELING OF NUCLEAR-DNA FRAGMENTATION [J].
GAVRIELI, Y ;
SHERMAN, Y ;
BENSASSON, SA .
JOURNAL OF CELL BIOLOGY, 1992, 119 (03) :493-501