Collagen-binding growth factors: Production and characterization of functional fusion proteins having a collagen-binding domain

被引:93
作者
Nishi, N [1 ]
Matsushita, O
Yuube, K
Miyanaka, H
Okabe, A
Wada, F
机构
[1] Kagawa Med Univ, Fac Med, Dept Endocrinol, Miki, Kagawa 7610793, Japan
[2] Kagawa Med Univ, Fac Med, Dept Microbiol, Miki, Kagawa 7610793, Japan
[3] Kagawa Med Univ, Fac Med, Res Equipment Ctr, Miki, Kagawa 7610793, Japan
关键词
D O I
10.1073/pnas.95.12.7018
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
0 The autocrine/paracrine peptide signaling molecules such as growth factors have many promising biologic activities for clinical applications. However, one cannot expect specific therapeutic effects of the factors administered by ordinary drug delivery systems as they have limited target specificity and short half-lives in vivo. To overcome the difficulties in using growth factors as therapeutic agents, we have produced fusion proteins consisting of growth factor moieties and a collagen-binding domain (CBD) derived from Clostridium histolyticum collagenase. The fusion proteins carrying the epidermal growth factor (EGF) or basic fibroblast growth factor (bFGF) at the N terminal of CBD (CBEGF/CBFGF) tightly bound to insoluble collagen and stimulated the growth of BALB/c 3T3 fibroblasts as much as the unfused counterparts; CBEGF, when injected subcutaneously into nude mice, remained at the sites of injection for up to 10 days, whereas EGF was not detectable 24 h after injection. Although CBEGF did not exert a growth-promoting effect in vivo, CBFGF, but not bFGF, strongly stimulated the DNA synthesis in stromal cells at 5 days and 7 days after injection. These results indicate that CBD may be used as an anchoring unit to produce fusion proteins nondiffusible and long-lasting in vivo.
引用
收藏
页码:7018 / 7023
页数:6
相关论文
共 17 条
[1]   TRANSMEMBRANE TGF-ALPHA PRECURSORS ACTIVATE EGF TGF-ALPHA RECEPTORS [J].
BRACHMANN, R ;
LINDQUIST, PB ;
NAGASHIMA, M ;
KOHR, W ;
LIPARI, T ;
NAPIER, M ;
DERYNCK, R .
CELL, 1989, 56 (04) :691-700
[2]  
Field SL, 1996, J CELL PHYSIOL, V168, P322, DOI 10.1002/(SICI)1097-4652(199608)168:2<322::AID-JCP11>3.0.CO
[3]  
2-5
[4]   THE MEMBRANE-PROTEIN CDB/DRAP-27 POTENTIATES THE JUXTACRINE GROWTH-FACTOR ACTIVITY OF THE MEMBRANE-ANCHORED HEPARIN-BINDING EGF-LIKE GROWTH-FACTOR [J].
HIGASHIYAMA, S ;
IWAMOTO, R ;
GOISHI, K ;
RAAB, G ;
TANIGUCHI, N ;
KLAGSBRUN, M ;
MEKADA, E .
JOURNAL OF CELL BIOLOGY, 1995, 128 (05) :929-938
[5]   CONSTRUCTION AND CHARACTERIZATION OF A FUSION PROTEIN WITH EPIDERMAL GROWTH-FACTOR AND THE CELL-BINDING DOMAIN OF FIBRONECTIN [J].
KAWASE, Y ;
OHDATE, Y ;
SHIMOJO, T ;
TAGUCHI, Y ;
KIMIZUKA, F ;
KATO, I .
FEBS LETTERS, 1992, 298 (2-3) :126-128
[6]  
KROCZKOWSKI B, 1989, MOL CELL BIOL, V9, P2771
[7]   Tethered epidermal growth factor as a paradigm for growth factor-induced stimulation from the solid phase [J].
Kuhl, PR ;
GriffithCima, LG .
NATURE MEDICINE, 1996, 2 (09) :1022-1027
[8]   Polypeptide growth factors in the nucleus: A review of function and translocation [J].
Levine, JE ;
Prystowsky, MB .
NEUROIMMUNOMODULATION, 1995, 2 (05) :290-298
[9]   A study of the collagen-binding domain of a 116-kDa Clostridium histolyticum collagenase [J].
Matsushita, O ;
Jung, CM ;
Minami, J ;
Katayama, S ;
Nishi, N ;
Okabe, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (06) :3643-3648
[10]   PARTIAL-PURIFICATION OF A MAJOR TYPE OF RAT PROSTATIC GROWTH-FACTOR - CHARACTERIZATION AS AN EPIDERMAL GROWTH FACTOR-RELATED MITOGEN [J].
NISHI, N ;
MATUO, Y ;
WADA, F .
PROSTATE, 1988, 13 (03) :209-220