Protein tyrosine kinase inhibitors synergize with nerve growth factor in embryonic chick sensory neuronal cell survival

被引:6
作者
Bartlett, SE
机构
[1] Division of Neuroscience, John Curtin Sch. of Medical Research, Australian National University, Canberra, ACT 2601
关键词
sensory neuronal cell survival; tyrosine kinase inhibitors; nerve growth factor; herbimycin; genistein; tyrphostin;
D O I
10.1016/S0304-3940(97)00318-2
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The survival of developing sensory neurons is dependent upon target-derived growth factors, in their absence neurons undergo programmed cell death. The molecular mechanisms underpinning neuronal cell survival and death are poorly understood. Tyrosine kinases are important signalling proteins that have been implicated in both cell survival and death. The aim of this study was to examine the effects of tyrosine kinase inhibition on embryonic chick sensory neuronal survival using the tyrosine kinase inhibitors, herbimycin, genistein and tyrphostin. In low concentrations of nerve growth factor, NGF (100 fg/ml), the majority of neurons die, however neuronal survival was significantly potentiated in the presence of each of the tyrosine kinase inhibitors, herbimycin (40 ng/ml), genistein (2.5 mu M) and tyrphostin (8 mu M). In the presence of each of these inhibitors, sensory neurons exhibited typical phase bright morphology and fibre outgrowth was increased. These results demonstrate that the tyrosine kinase inhibitors support the survival of neurons in the presence of low concentrations of NGF. Herbimycin was used at lower concentrations than previously reported, and at this concentration it has been shown to be noncytotoxic in animals. Therefore it will be important to determine if herbimycin can be used as a therapeutic agent for enhancing nerve regeneration following injury. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:87 / 90
页数:4
相关论文
共 24 条
[1]   TYRPHOSTINS INHIBIT PDGF-INDUCED DNA-SYNTHESIS AND ASSOCIATED EARLY EVENTS IN SMOOTH-MUSCLE CELLS [J].
BILDER, GE ;
KRAWIEC, JA ;
MCVETY, K ;
GAZIT, A ;
GILON, C ;
LYALL, R ;
ZILBERSTEIN, A ;
LEVITZKI, A ;
PERRONE, MH ;
SCHREIBER, AB .
AMERICAN JOURNAL OF PHYSIOLOGY, 1991, 260 (04) :C721-C730
[2]   AN ANALYSIS OF PERIPHERAL NEURONAL SURVIVAL FACTORS PRESENT IN MUSCLE [J].
BONYHADY, RE ;
HENDRY, IA ;
HILL, CE ;
WATTERS, DJ .
JOURNAL OF NEUROSCIENCE RESEARCH, 1985, 13 (03) :357-367
[3]   SRC GENE-PRODUCT OF TRANSFORMED AND MORPHOLOGICALLY REVERTED ASV-INFECTED MAMMALIAN-CELLS [J].
COLLETT, MS ;
BRUGGE, JS ;
ERIKSON, RL ;
LAU, AF ;
KRZYZEK, RA ;
FARAS, AJ .
NATURE, 1979, 281 (5728) :195-198
[4]   NEURITE EXTENSION AND PROTEIN TYROSINE PHOSPHORYLATION ELICITED BY INDUCIBLE EXPRESSION OF THE V-SRC ONCOGENE IN A PC12-CELL LINE [J].
COX, ME ;
MANESS, PF .
EXPERIMENTAL CELL RESEARCH, 1991, 195 (02) :423-431
[5]  
EISCHEN CM, 1994, J IMMUNOL, V153, P1947
[6]   Cell cycle blockers mimosine, ciclopirox, and deferoxamine prevent the death of PC12 cells and postmitotic sympathetic neurons after removal of trophic support [J].
Farinelli, SE ;
Greene, LA .
JOURNAL OF NEUROSCIENCE, 1996, 16 (03) :1150-1162
[7]   PROLIFERATIVE INHIBITION BY DOMINANT-NEGATIVE RAS RESCUES NAIVE AND NEURONALLY DIFFERENTIATED PC12 CELLS FROM APOPTOTIC DEATH [J].
FERRARI, G ;
GREENE, LA .
EMBO JOURNAL, 1994, 13 (24) :5922-5928
[8]   ERK1 AND ERK2, 2 MICROTUBULE-ASSOCIATED PROTEIN-2 KINASES, MEDIATE THE PHOSPHORYLATION OF TYROSINE-HYDROXYLASE AT SERINE-31 INSITU [J].
HAYCOCK, JW ;
AHN, NG ;
COBB, MH ;
KREBS, EG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (06) :2365-2369
[9]  
HONMA Y, 1992, CANCER RES, V52, P4017
[10]   ALTERED EXPRESSION OF PP60C-SRC INDUCED BY PERIPHERAL-NERVE INJURY [J].
IGNELZI, MA ;
PADILLA, SS ;
WARDER, DE ;
MANESS, PF .
JOURNAL OF COMPARATIVE NEUROLOGY, 1992, 315 (02) :171-177