Developmental expression of mouse Follistatin-like 1 (Fstl1):: Dynamic regulation during organogenesis of the kidney and lung

被引:67
作者
Adams, Derek [1 ]
Larman, Barry [1 ]
Oxburgh, Leif [1 ]
机构
[1] Maine Med Ctr, Res Inst, Scarborough, ME 04074 USA
关键词
Follistatin; Activin antagonist; BMP antagonist; bone development; gonad development; gut development; heart development; kidney development; limb development; lung development; neural development; skin development; tooth development;
D O I
10.1016/j.modgep.2006.10.009
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Follistatin-like 1 (Fst11) is a distantly related homolog of the Activin and Bone Morphogenetic Protein antagonist Follistatin. Interestingly, this molecule also has homology with the extracellular matrix modifying protein BM-40/SPARC/osteonectin. Previous studies in chick have identified Fst11 as a regulator of early mesoderm patterning, somitogenesis, myogenesis and neural development. In this study, we determine the developmental expression pattern of Fst11 in the mouse. We find that Fst11 is ubiquitously expressed in the early embryo,, and that expression becomes regionalized later during development. In the majority of tissues, Fst11 is strongly expressed in the mesenchymal component and excluded from the epithelium. Notable exceptions include the central nervous system, in which Fst11 expression is entirely absent with the exception of the choroid plexi and floor plate, the lung, in which Fst11 expression can be seen in airway epithelia and the kidney, in which collecting ducts and nascent nephron epithelia express the highest levels of Fst11. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:491 / 500
页数:10
相关论文
共 17 条
[1]   The expression and regulation of follistatin and a follistatin-like gene during avian somite compartmentalization and myogenesis [J].
Amthor, H ;
Connolly, D ;
Patel, K ;
BrandSaberi, B ;
Wilkinson, DG ;
Cooke, J ;
Christ, B .
DEVELOPMENTAL BIOLOGY, 1996, 178 (02) :343-362
[2]   SPARC, a matricellular protein: at the crossroads of cell-matrix [J].
Brekken, RA ;
Sage, EH .
MATRIX BIOLOGY, 2000, 19 (07) :569-580
[3]  
DALLPRA S, 2006, DEV BIOL
[4]   Structural characterization of TSC-36/Flik -: Analysis of two charge isoforms [J].
Hambrock, HO ;
Kaufmann, B ;
Müller, S ;
Hanisch, FG ;
Nose, K ;
Paulsson, M ;
Maurer, P ;
Hartmann, U .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (12) :11727-11735
[5]   Genome scanning with array CGH delineates regional alterations in mouse islet carcinomas [J].
Hodgson G. ;
Hager J.H. ;
Volik S. ;
Hariono S. ;
Wernick M. ;
Moore D. ;
Albertson D.G. ;
Pinkel D. ;
Collins C. ;
Hanahan D. ;
Gray J.W. .
Nature Genetics, 2001, 29 (4) :459-464
[6]   Regulation of a multigenic invasion programme by the transcription factor, AP-1: re-expression of a down-regulated gene, TSC-36, inhibits invasion [J].
Johnston, IMP ;
Spence, HJ ;
Winnie, JN ;
McGarry, L ;
Vass, JK ;
Meagher, L ;
Stapleton, G ;
Ozanne, BW .
ONCOGENE, 2000, 19 (47) :5348-5358
[7]   Granulosa cell-specific inactivation of follistatin causes female fertility defects [J].
Jorgez, CJ ;
Klysik, M ;
Jamin, SP ;
Behringer, RR ;
Matzuk, MM .
MOLECULAR ENDOCRINOLOGY, 2004, 18 (04) :953-967
[8]   Decrease in the expression of a novel TGF beta 1-inducible and ras-recision gene, TSC-36, in human cancer cells [J].
Mashimo, J ;
Maniwa, R ;
Sugino, H ;
Nose, K .
CANCER LETTERS, 1997, 113 (1-2) :213-219
[9]   MULTIPLE DEFECTS AND PERINATAL DEATH IN MICE DEFICIENT IN FOLLISTATIN [J].
MATZUK, MM ;
LU, NF ;
VOGEL, H ;
SELLHEYER, K ;
ROOP, DR ;
BRADLEY, A .
NATURE, 1995, 374 (6520) :360-363
[10]   TSC-36 (follistatin-related polypeptide) gene expression in estrogen receptor positive osteoblastic cell line, CDO7F [J].
Ohashi, T ;
Sato, S ;
Yoshiki, A ;
Kusakabe, M .
CALCIFIED TISSUE INTERNATIONAL, 1997, 61 (05) :400-403