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Functional domains of the FgfrL1 receptor.

Authors :
Gerber, Simon D.
Beauchamp, Philippe
Zhuang, Lei
Villiger, Peter M.
Trueb, Beat
Source :
Developmental Biology. May2020, Vol. 461 Issue 1, p43-54. 12p.
Publication Year :
2020

Abstract

FgfrL1 is a novel growth factor receptor that is primarily expressed in musculoskeletal tissues and the kidney. FgfrL1-deficient mice have a malformed diaphragm and no kidneys. Such animals die immediately after birth because they are not able to inflate their lungs. The FgfrL1 molecule is composed of three extracellular Ig domains, a transmembrane helix and a short intracellular domain. To investigate the contribution of each of these domains to the function of the novel receptor, we generated mice with deletions of the individual domains. Mice lacking the intracellular domain are viable and phenotypically normal. Mice lacking the first (N-terminal) Ig domain are also viable and normal, but have a reduced life span. Mice lacking the Ig2 or the Ig3 domain are born alive, but die within 24 ​h after birth. Ig2-deficient animals exhibit substantially smaller kidneys than wild-type littermates and contain a lower number of glomeruli. Ig3-deficient mice completely lack metanephric kidneys. Interestingly, both the Ig2 and the Ig3-deficient animals show only minor alterations in the diaphragm, which still enables them to inflate their lungs after birth. Our results demonstrate that the principal function of the FgfrL1 receptor is to control the growth of the metanephric kidneys by regulating nephrogenesis. It appears that this function is primarily accomplished by the Ig3 domain with some contribution of the Ig2 domain. It is conceivable that the two domains interact with an Fgf ligand and another molecule from the surface of neighboring cells to induce condensation of the metanephric mesenchyme to renal epithelia and glomeruli. • Receptor FgfrL1 contains 3 extracellular Ig domains and an intracellular tail. • Ig1-deficient mice are normal but have a reduced life span. • Ig2-deficient mice have smaller kidneys and die within 24 ​h after birth. • Ig3-deficient animals have no kidneys and die within 24 ​h after birth. • Thus, FgfrL1 primarily controls nephrogenesis and the Ig3 domain is most important. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00121606
Volume :
461
Issue :
1
Database :
Academic Search Index
Journal :
Developmental Biology
Publication Type :
Academic Journal
Accession number :
142734978
Full Text :
https://doi.org/10.1016/j.ydbio.2020.01.003