Shh/Gli Signalling during Murine Lung Development

Author(s):  
Martin Rutter ◽  
Martin Post
Keyword(s):  
Author(s):  
Erik Melén ◽  
Alvin Kho ◽  
Sunita Sharma ◽  
Roger Gaedigk ◽  
Steven J. Leeder ◽  
...  

Development ◽  
1991 ◽  
Vol 112 (2) ◽  
pp. 551-558 ◽  
Author(s):  
J. Roman ◽  
C.W. Little ◽  
J.A. McDonald

Cell-matrix interactions are generally considered critical for normal lung development. This is particularly likely to be true during the glandular stage, when the primitive airways are formed through a process termed branching morphogenesis. Integrins, transmembrane receptors that bind to extracellular matrices, are likely to mediate important interactions between embryonic cells and their matrices during branching morphogenesis. In this report, we examine the role of integrin receptors in this process. Immunohistochemical studies revealed that the integrins VLA 3, VLA 5 and integrin receptors to vitronectin are expressed in the epithelium and/or mesenchyme during the glandular stage of murine lung development. To correlate expression with function, an in vitro model of murine lung branching morphogenesis was utilized to examine branching in the presence of inhibitors of ligand binding to integrin receptors. One such reagent, a hexapeptide containing the RGD (Arg-Gly-Asp) sequence, diminished branching and resulted in an abnormal morphology, whereas a control peptide RGESP (Arg-Gly-Glu-Ser-Pro) had no effect. These findings suggest a critical role for cell-matrix interactions mediated via integrin receptors in early stages of mammalian lung development.


Development ◽  
1998 ◽  
Vol 125 (18) ◽  
pp. 3615-3623 ◽  
Author(s):  
M. Weinstein ◽  
X. Xu ◽  
K. Ohyama ◽  
C.X. Deng

Mammalian lungs begin as an outpocket of the foregut, and depend on multiple stages of branching morphogenesis and alveogenesis to reach their final form. An examination of fgf receptor gene expression indicated that all four receptors (fgfr-1 to fgfr-4) are expressed in postnatal lungs at varying levels. We show that mice homozygous for a targeted mutation of fgfr-4 exhibited no overt abnormalities in the lungs or any other organ. However, mice doubly homozygous for disruptions of the fgfr-3 and fgfr-4 genes display novel phenotypes not present in either single mutant, which include pronounced dwarfism and lung abnormalities. Lungs of fgfr-3(−/−)fgfr-4(−/−)animals, which are normal at birth, are completely blocked in alveogenesis and do not form secondary septae to delimit alveoli. Consequently, air spaces in the lung are expanded and no alveoli can be seen. The mutant lungs failed to downregulate postnatal elastin deposition despite their normal levels of surfactant expression and cell proliferation. These data revealed a cooperative function of FGFR-3 and FGFR-4 to promote the formation of alveoli during postnatal lung development.


2011 ◽  
Vol 12 (1) ◽  
Author(s):  
Erik Melén ◽  
Alvin T Kho ◽  
Sunita Sharma ◽  
Roger Gaedigk ◽  
J Steven Leeder ◽  
...  

2003 ◽  
Vol 51 (10) ◽  
pp. 1307-1315 ◽  
Author(s):  
Teresa E. Wagner ◽  
Charles W. Frevert ◽  
Erica L. Herzog ◽  
Lynn M. Schnapp

2013 ◽  
Vol 13 (1) ◽  
pp. 13 ◽  
Author(s):  
Sana Mujahid ◽  
Tanya Logvinenko ◽  
MaryAnn V Volpe ◽  
Heber C Nielsen

Blood ◽  
2018 ◽  
Vol 132 (11) ◽  
pp. 1167-1179 ◽  
Author(s):  
Nagaharu Tsukiji ◽  
Osamu Inoue ◽  
Mitsuru Morimoto ◽  
Norifumi Tatsumi ◽  
Hiroaki Nagatomo ◽  
...  

Key Points Association of platelet Clec-2 with lymphatic podoplanin regulates lung development by facilitating alveolar duct myofibroblast differentiation. Alveolar duct myofibroblast differentiation is regulated in part by transforming growth factor-β released from platelets activated by Clec-2/podoplanin interaction.


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