TY - JOUR
T1 - Amino acid transporter LAT3 is required for podocyte development and function
AU - Sekine, Yuji
AU - Nishibori, Yukino
AU - Akimoto, Yoshihiro
AU - Kudo, Akihiko
AU - Ito, Noriko
AU - Fukuhara, Daisuke
AU - Kurayama, Ryota
AU - Higashihara, Eiji
AU - Babu, Ellappan
AU - Kanai, Yoshikatsu
AU - Asanuma, Katsuhiko
AU - Nagata, Michio
AU - Majumdar, Årindam
AU - Tryggvason, Karl
AU - Yan, Kunimasa
PY - 2009/7
Y1 - 2009/7
N2 - LAT3 is a Na+-independent neutral L-amino acid transporter recently isolated from a human hepatocellular carcinoma cell line. Although liver, skeletal muscle, and pancreas are known to express LAT3, the tissue distribution and physiologic function of this transporter are not completely understood. Here, we observed that glomeruli express LAT3. Immunofluorescence, confocal microscopy, and immunoelectron microscopy revealed that LAT3 localizes to the apical plasma membrane of podocyte foot processes. In mice, starvation upregulated glomerular LAT3, phosphorylated AKT1, reconstituted the actin network, and elongated foot processes. In the fetal kidney, we observed intense LAT3 expression at the capillary loops stage of renal development. Finally, zebrafish morphants lacking lat3 function showed collapsed glomeruli with thickened glomerular basement membranes. Permeability studies of the glomerular filtration barrier in these zebrafish morphants demonstrated a disruption of selective glomerular permeability. Our data suggest that LAT3 may play a crucial role in the development and maintenance of podocyte structure and function by regulating protein synthesis and the actin cytoskeleton.
AB - LAT3 is a Na+-independent neutral L-amino acid transporter recently isolated from a human hepatocellular carcinoma cell line. Although liver, skeletal muscle, and pancreas are known to express LAT3, the tissue distribution and physiologic function of this transporter are not completely understood. Here, we observed that glomeruli express LAT3. Immunofluorescence, confocal microscopy, and immunoelectron microscopy revealed that LAT3 localizes to the apical plasma membrane of podocyte foot processes. In mice, starvation upregulated glomerular LAT3, phosphorylated AKT1, reconstituted the actin network, and elongated foot processes. In the fetal kidney, we observed intense LAT3 expression at the capillary loops stage of renal development. Finally, zebrafish morphants lacking lat3 function showed collapsed glomeruli with thickened glomerular basement membranes. Permeability studies of the glomerular filtration barrier in these zebrafish morphants demonstrated a disruption of selective glomerular permeability. Our data suggest that LAT3 may play a crucial role in the development and maintenance of podocyte structure and function by regulating protein synthesis and the actin cytoskeleton.
UR - https://www.scopus.com/pages/publications/67649687026
UR - https://www.scopus.com/inward/citedby.url?scp=67649687026&partnerID=8YFLogxK
U2 - 10.1681/ASN.2008070809
DO - 10.1681/ASN.2008070809
M3 - Article
C2 - 19443642
AN - SCOPUS:67649687026
SN - 1046-6673
VL - 20
SP - 1586
EP - 1596
JO - Journal of the American Society of Nephrology
JF - Journal of the American Society of Nephrology
IS - 7
ER -