Human metalloprotease-disintegrin Kuzbanian regulates sympathoadrenal cell fate in development and neoplasia

被引:57
作者
Yavari, R
Adida, C
Bray-Ward, P
Brines, M
Xu, T
机构
[1] Yale Univ, Sch Med, Howard Hughes Med Inst, Boyer Ctr Mol Med, New Haven, CT 06536 USA
[2] Yale Univ, Sch Med, Dept Genet, Boyer Ctr Mol Med, New Haven, CT 06536 USA
[3] Yale Univ, Sch Med, Dept Med, Boyer Ctr Mol Med, New Haven, CT 06536 USA
[4] Yale Univ, Sch Med, Dept Pathol, Boyer Ctr Mol Med, New Haven, CT 06536 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1093/hmg/7.7.1161
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
The development of the sympathetic nervous system involves cell-cell interactions that regulate the fate and migration of progenitor neural cells. Recent evidence shows that focal membrane-bound protease activity is critical for such interactions. The Drosophila kuzbanian (kuz) gene is required in neurogenesis and encodes a highly conserved, membrane-bound metalloprotease-disintegrin closley related to the TNF-alpha converting enzyme (TACE). We have characterized the human and mouse kuz homologs and mapped human kuz to chromosome 15q22. During mouse embryonic development Kuz is expressed mainly in the sympathoadrenal and olfactory neural precursors. Once sympathoadrenal cells differentiate into chromaffin cells in the adult adrenal medulla, they no longer express Kuz. However, we found that tumors of sympathoadrenal origin, such as pheochromocytomas and neuroblastomas, overexpress Kuz. Further, transfection of a kuz construct lacking the protease domain, but not the full-length construct, induces neurite formation in PC12 chromaffin tumor cells. Taken together our results suggest a critical role for Kuz in regulation of sympathoadrenal cell fate.
引用
收藏
页码:1161 / 1167
页数:7
相关论文
共 26 条
[1]   MOLECULAR CONTROL OF CELL FATE IN THE NEURAL CREST - THE SYMPATHOADRENAL LINEAGE [J].
ANDERSON, DJ .
ANNUAL REVIEW OF NEUROSCIENCE, 1993, 16 :129-158
[2]   IDENTIFICATION OF A HUMAN ACHAETE-SCUTE HOMOLOG HIGHLY EXPRESSED IN NEUROENDOCRINE TUMORS [J].
BALL, DW ;
AZZOLI, CG ;
BAYLIN, SB ;
CHI, D ;
DOU, SS ;
DONISKELLER, H ;
CUMARASWAMY, A ;
BORGES, M ;
NELKIN, BD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (12) :5648-5652
[3]   Focalized proteolysis: Spatial and temporal regulation of extracellular matrix degradation at the cell surface [J].
Basbaum, CB ;
Werb, Z .
CURRENT OPINION IN CELL BIOLOGY, 1996, 8 (05) :731-738
[4]   A metalloproteinase disintegrin that releases tumour-necrosis factor-alpha from cells [J].
Black, RA ;
Rauch, CT ;
Kozlosky, CJ ;
Peschon, JJ ;
Slack, JL ;
Wolfson, MF ;
Castner, BJ ;
Stocking, KL ;
Reddy, P ;
Srinivasan, S ;
Nelson, N ;
Boiani, N ;
Schooley, KA ;
Gerhart, M ;
Davis, R ;
Fitzner, JN ;
Johnson, RS ;
Paxton, RJ ;
March, CJ ;
Cerretti, DP .
NATURE, 1997, 385 (6618) :729-733
[5]   A POTENTIAL FUSION PEPTIDE AND AN INTEGRIN LIGAND DOMAIN IN A PROTEIN ACTIVE IN SPERM-EGG FUSION [J].
BLOBEL, CP ;
WOLFSBERG, TG ;
TURCK, CW ;
MYLES, DG ;
PRIMAKOFF, P ;
WHITE, JM .
NATURE, 1992, 356 (6366) :248-252
[6]   Integration of the cytogenetic, genetic, and physical maps of the human genome by FISH mapping of CEPH YAC clones [J].
BrayWard, P ;
Menninger, J ;
Lieman, J ;
Desai, T ;
Mokady, N ;
Banks, A ;
Ward, DC .
GENOMICS, 1996, 32 (01) :1-14
[7]   A NOVEL METALLOPROTEINASE ORIGINALLY ISOLATED FROM BRAIN MYELIN MEMBRANES IS PRESENT IN MANY TISSUES [J].
CHANTRY, A ;
GLYNN, P .
BIOCHEMICAL JOURNAL, 1990, 268 (01) :245-248
[8]  
CHANTRY A, 1989, J BIOL CHEM, V264, P21603
[9]  
DOUARIN NML, 1994, CURR OPIN GENE DEV, V4, P685
[10]   The cell surface metalloprotease disintegrin Kuzbanian is required for axonal extension in Drosophila [J].
Fambrough, D ;
Pan, DJ ;
Rubin, GM ;
Goodman, CS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (23) :13233-13238