ERK and MMPs sequentially regulate distinct stages of epithelial tubule development

被引:133
作者
O'Brien, LE
Tang, K
Kats, ES
Schutz-Geschwender, A
Lipschutz, JH
Mostov, KE
机构
[1] Univ Calif San Francisco, Dept Biochem & Biophys, Dept Anat, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Cardiovasc Res Inst, San Francisco, CA 94143 USA
[3] LI COR Inc, Lincoln, NE 68504 USA
[4] Univ Penn, Dept Med, Philadelphia, PA 19104 USA
[5] Univ Penn, Cell & Mol Biol Grad Grp, Philadelphia, PA 19104 USA
[6] Vet Adm Med Ctr, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/j.devcel.2004.06.001
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epithelial cells undergo tubulogenesis in response to morphogens such as hepatocyte growth factor (HGF). To organize into tubules, cells must execute a complex series of morphogenetic events; however, the mechanisms that underlie the timing and sequence of these events are poorly understood. Here, we show that downstream effectors of HGF coordinately regulate successive stages of tubulogenesis. Activation of extracellular-regulated kinase [ERK) is necessary and sufficient for the initial stage, during which cells depolarize and migrate. ERK becomes dispensable for the latter stage, during which cells repolarize and differentiate. Conversely, the activity of matrix metalloproteases (MMPs) is essential for the late stage but not the initial stage. Thus, ERK and MMPs define two regulatory subprograms that act in sequence. By inducing these reciprocal signals, HGF directs the morphogenetic progression of tubule development.
引用
收藏
页码:21 / 32
页数:12
相关论文
共 38 条
[1]   Metalloproteinase inhibitors: biological actions and therapeutic opportunities [J].
Baker, AH ;
Edwards, DR ;
Murphy, G .
JOURNAL OF CELL SCIENCE, 2002, 115 (19) :3719-3727
[2]   Gene expression alterations during HGF-induced dedifferentiation of a renal tubular epithelial cell line (MDCK) using a novel canine DNA microarray [J].
Balkovetz, DF ;
Gerrard, ER ;
Li, SX ;
Johnson, D ;
Lee, J ;
Tobias, JW ;
Rogers, KK ;
Snyder, RW ;
Lipschutz, JH .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2004, 286 (04) :F702-F710
[3]  
Fisher CE, 2001, DEVELOPMENT, V128, P4329
[4]   Hepatocyte growth factor modulates matrix metalloproteinases and plasminogen activator/plasmin proteolytic pathways in progressive renal interstitial fibrosis [J].
Gong, R ;
Rifai, A ;
Tolbert, EM ;
Centracchio, JN ;
Dworkin, LD .
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY, 2003, 14 (12) :3047-3060
[5]   Induced expression of Rnd3 is associated with transformation of polarized epithelial cells by the Raf-MEK-extracellular signal-regulated kinase pathway [J].
Hansen, SH ;
Zegers, MMP ;
Woodrow, M ;
Rodriguez-Viciana, P ;
Chardin, P ;
Mostov, KE ;
McMahon, M .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (24) :9364-9375
[6]   TRANSFORMATIONS BETWEEN EPITHELIUM AND MESENCHYME - NORMAL, PATHOLOGICAL, AND EXPERIMENTALLY-INDUCED [J].
HAY, ED ;
ZUK, A .
AMERICAN JOURNAL OF KIDNEY DISEASES, 1995, 26 (04) :678-690
[7]   Matrix metalloproteinases regulate neovascularization by acting as pericellular fibrinolysins [J].
Hiraoka, N ;
Allen, E ;
Apel, IJ ;
Gyetko, MR ;
Weiss, SJ .
CELL, 1998, 95 (03) :365-377
[8]   Molecular mechanisms of tubulogenesis [J].
Hogan, BLM ;
Kolodziej, PA .
NATURE REVIEWS GENETICS, 2002, 3 (07) :513-523
[9]   Regulation of cell invasion and morphogenesis in a three-dimensional type I collagen matrix by membrane-type matrix metalloproteinases 1, 2, and 3 [J].
Hotary, K ;
Allen, E ;
Punturieri, A ;
Yana, I ;
Weiss, SJ .
JOURNAL OF CELL BIOLOGY, 2000, 149 (06) :1309-1323
[10]   Membrane type I matrix metalloproteinase usurps tumor growth control imposed by the three-dimensional extracellular matrix [J].
Hotary, KB ;
Allen, ED ;
Brooks, PC ;
Datta, NS ;
Long, MW ;
Weiss, SJ .
CELL, 2003, 114 (01) :33-45