PUBLICATION
Mapping of the amniotic fluid proteome of fetuses with congenital anomalies of the kidney and urinary tract identifies Plastin 3 as a protein involved in glomerular integrity
- Authors
- Fédou, C., Camus, M., Lescat, O., Feuillet, G., Mueller, I., Ross, B., Buléon, M., Neau, E., Alves, M., Goudounéche, D., Breuil, B., Boizard, F., Bardou, Q., Casemayou, A., Tack, I., Dreux, S., Batut, J., Blader, P., Burlet-Schiltz, O., Decramer, S., Wirth, B., Klein, J., Saulnier-Blache, J.S., Buffin-Meyer, B., Schanstra, J.P.
- ID
- ZDB-PUB-210515-12
- Date
- 2021
- Source
- The Journal of pathology 254(5): 575-588 (Journal)
- Registered Authors
- Keywords
- CAKUT, amniotic fluid, chronic kidney disease, fetus, nephrogenesis, plastin-3, podocyte, proteomics
- MeSH Terms
-
- Amniotic Fluid/metabolism*
- Animals
- Female
- Fetus
- Humans
- Male
- Membrane Glycoproteins/metabolism*
- Mice
- Microfilament Proteins/metabolism*
- Proteome
- Proteomics
- Urogenital Abnormalities/metabolism*
- Vesico-Ureteral Reflux/metabolism*
- Zebrafish
- PubMed
- 33987838 Full text @ J. Pathol.
Citation
Fédou, C., Camus, M., Lescat, O., Feuillet, G., Mueller, I., Ross, B., Buléon, M., Neau, E., Alves, M., Goudounéche, D., Breuil, B., Boizard, F., Bardou, Q., Casemayou, A., Tack, I., Dreux, S., Batut, J., Blader, P., Burlet-Schiltz, O., Decramer, S., Wirth, B., Klein, J., Saulnier-Blache, J.S., Buffin-Meyer, B., Schanstra, J.P. (2021) Mapping of the amniotic fluid proteome of fetuses with congenital anomalies of the kidney and urinary tract identifies Plastin 3 as a protein involved in glomerular integrity. The Journal of pathology. 254(5):575-588.
Abstract
Congenital anomalies of the kidney and the urinary tract (CAKUT) are the first cause of chronic kidney disease in childhood. Several genetic and environmental origins are associated with CAKUT, but most pathogenic pathways remain elusive. Considering the amniotic fluid (AF) composition as a proxy for fetal kidney development, we analyzed the AF proteome from non-severe CAKUT (n=19), severe CAKUT (n=14), and healthy control (n=22) fetuses using LC-MS/MS. We identified 471 significant proteins that discriminated the 3 AF groups with 81% precision. Among them, 8 proteins independent of gestational age (CSPG4, LMAN2, ENDOD1, ANGPTL2, PRSS8, NGFR, ROBO4, PLS3) were associated to both the presence and the severity of CAKUT. Among those, 5 were part of a protein-protein interaction network involving proteins previously identified as being potentially associated to CAKUT. The actin-bundling protein PLS3 (plastin 3) was the only protein displaying a gradually increased AF abundance from control via non-severe, to severe CAKUT. Immunohistochemistry experiments showed that PLS3 was expressed in the human fetal as well as in both the fetal and post-natal mouse kidney. In zebrafish embryos, depletion of PLS3 led to a general disruption of embryonic growth including reduced pronephros development. In postnatal Pls3 knockout mice, kidneys were macroscopically normal, but the glomerular ultrastructure showed thickening of the basement membrane and fusion of podocyte foot processes. These structural changes were associated with albuminuria and decreased expression of podocyte markers including Wilms' tumor 1 protein, nephrin and podocalyxin. In conclusion, we provide the first map of the CAKUT AF proteome that will serve as a reference for future studies. Among the proteins strongly associated with CAKUT, PLS3 did surprisingly not specifically affect nephrogenesis but was found as a new contributor in the maintenance of normal kidney function, at least in part through the control of glomerular integrity. This article is protected by copyright. All rights reserved.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping