TY - JOUR
T1 - Molecular dissection of laminin α5 in vivo reveals separable domain-specific roles in embryonic development and kidney function
AU - Kikkawa, Yamato
AU - Miner, Jeffrey H.
N1 - Funding Information:
We thank Gloriosa Go, Cong Li, and Jennifer Richardson for technical assistance; the Mouse Genetics Core at Washington University School of Medicine for generating and caring for transgenic mice; and Marilyn Levy and Jeanette Cunningham for electron microscopy support. We also thank Ismo Virtanen, Peter Yurchenco, Albert Chung, Peter Marinkovich, Joshua Sanes, Rupert Timpl, Takako Sasaki, and Corinne Antignac forproviding antibodies and plasmids. This work was supportedbygrants to JHM from the NIH (R01DK064687 and R01GM060432) and the March of Dimes (#FY02-192) and in part by research grants to YK from The Akiyama Foundation. JHM is an Established Investigator of the American Heart Association.
PY - 2006/8/1
Y1 - 2006/8/1
N2 - Laminins are a family of basement membrane proteins with diverse roles in fundamental developmental processes such as epiblast polarization and gastrulation, as well as in organ development and function. We have focused on the laminin α1 and α5 chains, the ancestral laminin α chains required for development. To elucidate the unique functions of laminin α1 and α5 and their COOH-terminal LG domains, we have produced a collection of laminin knockout and transgenic mice expressing full length and chimeric laminin α5/α1 chains. Crossing the transgenes onto the Lama5-/- background generates "pseudo-knockins", so called because endogenous laminin α5 is replaced by transgene-encoded proteins. Expression of a chimera with the entire α5LG domain replaced by α1LG had minimal ameliorative effects on the defects observed in Lama5-/- embryos. In contrast, high level expression of a chimera with only the α5LG3-5 tandem replaced by α1LG3-5 completely rescued defects in digit septation, neural tube closure, placental labyrinth morphology, lung lobe septation, hair growth, and vascularization of kidney glomeruli. These mice were viable for several months, but they developed a lethal nephrotic syndrome. Our results show that: (1) the laminin α5LG1-2 tandem plays an essential role during development and harbors the great majority of the functionality of the α5LG domain; and (2) the α5LG3-5 tandem serves as a novel determinant required for the kidney's glomerular filtration barrier to plasma protein.
AB - Laminins are a family of basement membrane proteins with diverse roles in fundamental developmental processes such as epiblast polarization and gastrulation, as well as in organ development and function. We have focused on the laminin α1 and α5 chains, the ancestral laminin α chains required for development. To elucidate the unique functions of laminin α1 and α5 and their COOH-terminal LG domains, we have produced a collection of laminin knockout and transgenic mice expressing full length and chimeric laminin α5/α1 chains. Crossing the transgenes onto the Lama5-/- background generates "pseudo-knockins", so called because endogenous laminin α5 is replaced by transgene-encoded proteins. Expression of a chimera with the entire α5LG domain replaced by α1LG had minimal ameliorative effects on the defects observed in Lama5-/- embryos. In contrast, high level expression of a chimera with only the α5LG3-5 tandem replaced by α1LG3-5 completely rescued defects in digit septation, neural tube closure, placental labyrinth morphology, lung lobe septation, hair growth, and vascularization of kidney glomeruli. These mice were viable for several months, but they developed a lethal nephrotic syndrome. Our results show that: (1) the laminin α5LG1-2 tandem plays an essential role during development and harbors the great majority of the functionality of the α5LG domain; and (2) the α5LG3-5 tandem serves as a novel determinant required for the kidney's glomerular filtration barrier to plasma protein.
KW - Basement membrane
KW - Kidney
KW - Laminin
KW - Placenta
KW - Syndactyly
UR - http://www.scopus.com/inward/record.url?scp=33745969114&partnerID=8YFLogxK
U2 - 10.1016/j.ydbio.2006.04.463
DO - 10.1016/j.ydbio.2006.04.463
M3 - Article
C2 - 16750824
AN - SCOPUS:33745969114
SN - 0012-1606
VL - 296
SP - 265
EP - 277
JO - Developmental Biology
JF - Developmental Biology
IS - 1
ER -