Novel betacellulin derivatives - Separation of the differentiation activity from the mitogenic activity

被引:5
作者
Itoh, T [1 ]
Kondo, M [1 ]
Tanaka, Y [1 ]
Kobayashi, M [1 ]
Sasada, R [1 ]
Igarashi, K [1 ]
Suenaga, M [1 ]
Koyama, N [1 ]
Nishimura, O [1 ]
Fujino, M [1 ]
机构
[1] Takeda Chem Ind Ltd, Div Pharmaceut Res, Discovery Res Labs 1, Tsukuba, Ibaraki 3004293, Japan
关键词
D O I
10.1074/jbc.M106603200
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
Betacellulin (BTC) is a member of the epidermal growth factor family. It has two biological activities: mitogenic activity in fibroblasts and vascular smooth muscle cells, and differentiation activity for the differentiation of pancreatic acinar AR42J cells into insulin-secreting cells. The previous finding that recombinant BTC promotes the neogenesis of beta -cells in a mouse model supports the possibility that BTC is a therapeutic protein. However, the mitogenic activity of BTC may not be needed for differentiation into beta -cells and may cause a side effect in clinical use. We prepared several derivatives of BTC to segregate the two activities, to decrease the mitogenic activity, and to maintain the differentiation activity. We succeeded in obtaining BTC derivatives segregated by the two biological activities by preparing truncated-type derivatives. A derivative of BTC, BTC24-76, with a truncated N-terminal 23 amino acids and C-terminal 4 amino acids, was 2.5-fold more active in differentiation and had one-tenth of the mitogenic activity. The derivatives described in the present study should be helpful in future applications as therapeutic proteins and in basic research for discovery of a BTC-specific receptor.
引用
收藏
页码:40698 / 40703
页数:6
相关论文
共 46 条
[1]   Epidermal growth factor and betacellulin mediate signal transduction through co-expressed ErbB2 and ErbB3 receptors [J].
Alimandi, M ;
Wang, LM ;
Bottaro, D ;
Lee, CC ;
Kuo, A ;
Frankel, M ;
Fedi, P ;
Tang, C ;
Lippman, M ;
Pierce, JH .
EMBO JOURNAL, 1997, 16 (18) :5608-5617
[2]   HUMAN EPIDERMAL GROWTH-FACTOR PRECURSOR - CDNA SEQUENCE, EXPRESSION INVITRO AND GENE ORGANIZATION [J].
BELL, GI ;
FONG, NM ;
STEMPIEN, MM ;
WORMSTED, MA ;
CAPUT, D ;
KU, L ;
URDEA, MS ;
RALL, LB ;
SANCHEZPESCADOR, R .
NUCLEIC ACIDS RESEARCH, 1986, 14 (21) :8427-8446
[3]   SECRETED PLACENTAL ALKALINE-PHOSPHATASE - A POWERFUL NEW QUANTITATIVE INDICATOR OF GENE-EXPRESSION IN EUKARYOTIC CELLS [J].
BERGER, J ;
HAUBER, J ;
HAUBER, R ;
GEIGER, R ;
CULLEN, BR .
GENE, 1988, 66 (01) :1-10
[4]   MURINE EPIDERMAL GROWTH-FACTOR - STRUCTURE AND FUNCTION [J].
BURGESS, AW ;
LLOYD, CJ ;
SMITH, S ;
STANLEY, E ;
WALKER, F ;
FABRI, L ;
SIMPSON, RJ ;
NICE, EC .
BIOCHEMISTRY, 1988, 27 (14) :4977-4985
[5]   CONSTRUCTION AND SELECTION OF RECOMBINANT PLASMIDS CONTAINING FULL-LENGTH COMPLEMENTARY DNAS CORRESPONDING TO RAT INSULIN-I AND INSULIN-II [J].
CHAN, SJ ;
NOYES, BE ;
AGARWAL, KL ;
STEINER, DF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (10) :5036-5040
[6]   PANCREATIC TUMORAL CELL-LINE AR42J - AN AMPHICRINE MODEL [J].
CHRISTOPHE, J .
AMERICAN JOURNAL OF PHYSIOLOGY, 1994, 266 (06) :G963-G971
[7]   HUMAN TRANSFORMING GROWTH FACTOR-ALPHA - PRECURSOR STRUCTURE AND EXPRESSION IN ESCHERICHIA-COLI [J].
DERYNCK, R ;
ROBERTS, AB ;
WINKLER, ME ;
CHEN, EY ;
GOEDDEL, DV .
CELL, 1984, 38 (01) :287-297
[8]   STRUCTURE-FUNCTION ANALYSIS OF EPIDERMAL GROWTH-FACTOR - SITE DIRECTED MUTAGENESIS AND NUCLEAR-MAGNETIC-RESONANCE [J].
DUDGEON, TJ ;
COOKE, RM ;
BARON, M ;
CAMPBELL, ID ;
EDWARDS, RM ;
FALLON, A .
FEBS LETTERS, 1990, 261 (02) :392-396
[9]   Identification of betacellulin as a major peptide growth factor in milk: purification, characterization and molecular cloning of bovine betacellulin [J].
Dunbar, AJ ;
Priebe, IK ;
Belford, DA ;
Goddard, C .
BIOCHEMICAL JOURNAL, 1999, 344 :713-721
[10]   Structure-function and biological role of betacellulin [J].
Dunbar, AJ ;
Goddard, C .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2000, 32 (08) :805-815