FGF10 controls the patterning of the tracheal cartilage rings via Shh

被引:72
作者
Sala, Frederic G. [1 ]
Del Moral, Pierre-Marie [1 ]
Tiozzo, Caterina [1 ]
Al Alam, Denise [1 ]
Warburton, David [1 ]
Grikscheit, Tracy [1 ]
Veltmaat, Jacqueline M. [1 ]
Bellusci, Saverio [1 ,2 ]
机构
[1] Childrens Hosp Los Angeles, Saban Res Inst, Dev Biol & Regenerat Med Program, Los Angeles, CA 90027 USA
[2] Univ Giessen, Dept Internal Med 2, Lung Ctr, D-35392 Giessen, Germany
来源
DEVELOPMENT | 2011年 / 138卷 / 02期
关键词
Fgf10; Shh; Trachea; Cartilage formation; Mouse; MORPHOGENESIS; EXPRESSION; INDUCTION; ROLES; CELLS; MODEL; BMP4;
D O I
10.1242/dev.051680
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
During embryonic development, appropriate dorsoventral patterning of the trachea leads to the formation of periodic cartilage rings from the ventral mesenchyme and continuous smooth muscle from the dorsal mesenchyme. In this work, we have investigated the role of two crucial morphogens, fibroblast growth factor 10 and sonic hedgehog, in the formation of periodically alternating cartilaginous and non-cartilaginous domains in the ventral mesenchyme. Using a combination of gain- and loss-of-function approaches for FGF10 and SHH, we demonstrate that precise spatio-temporal patterns and appropriate levels of expression of these two signaling molecules in the ventral area are crucial between embryonic day 11.5 and 13.5 for the proper patterning of the cartilage rings. We conclude that the expression level of FGF10 in the mesenchyme has to be within a critical range to allow for periodic expression of Shh in the ventral epithelium, and consequently for the correct patterning of the cartilage rings. We propose that disturbed balances of Fgf10 and Shh may explain a subset of human tracheomalacia without tracheo-esophageal fistula or tracheal atresia.
引用
收藏
页码:273 / 282
页数:10
相关论文
共 30 条
  • [1] AKIYAMA H, 2004, DEVELOPMENT, V18, P1072
  • [2] AUSTIN J, 2003, DEV DEV, V13, P3
  • [3] Bellusci S, 1997, DEVELOPMENT, V124, P4867
  • [4] Conditional and inducible transgene expression in mice through the combinatorial use of Cre-mediated recombination and tetracycline induction
    Belteki, G
    Haigh, J
    Kabacs, N
    Haigh, K
    Sison, K
    Costantini, F
    Whitsett, J
    Quaggin, SE
    Nagy, A
    [J]. NUCLEIC ACIDS RESEARCH, 2005, 33 (05) : 1 - 10
  • [5] BERG T, 2007, DEV DEV, V46, P1187
  • [6] FGF-10 disrupts lung morphogenesis and causes pulmonary adenomas in vivo
    Clark, JC
    Tichelaar, JW
    Wert, SE
    Itoh, N
    Perl, AKT
    Stahlman, MT
    Whitsett, JA
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2001, 280 (04) : L705 - L715
  • [7] CLOCK AND WAVEFRONT MODEL FOR CONTROL OF NUMBER OF REPEATED STRUCTURES DURING ANIMAL MORPHOGENESIS
    COOKE, J
    ZEEMAN, EC
    [J]. JOURNAL OF THEORETICAL BIOLOGY, 1976, 58 (02) : 455 - 476
  • [8] DasGupta R, 1999, DEVELOPMENT, V126, P4557
  • [9] De Moerlooze L, 2000, DEVELOPMENT, V127, P483
  • [10] THEORY OF BIOLOGICAL PATTERN FORMATION
    GIERER, A
    MEINHARDT, H
    [J]. KYBERNETIK, 1972, 12 (01): : 30 - 39