Cell Biology
The human nephrin Y1139RSL motif is essential for podocyte foot process organization and slit diaphragm formation during glomerular developmentNephrin endocytosis and glomerular development

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Nephrin is an immunoglobulin-type cell-adhesion molecule with a key role in the glomerular interpodocyte slit diaphragm. Mutations in the nephrin gene are associated with defects in the slit diaphragm, leading to early-onset nephrotic syndrome, typically resistant to treatment. Although the endocytic trafficking of nephrin is essential for the assembly of the slit diaphragm, nephrin's specific endocytic motifs remain unknown. To search for endocytic motifs, here we performed a multisequence alignment of nephrin and identified a canonical YXXØ-type motif, Y1139RSL, in the nephrin cytoplasmic tail, expressed only in primates. Using site-directed mutagenesis, various biochemical methods, single-plane illumination microscopy, a human podocyte line, and a human nephrin-expressing zebrafish model, we found that Y1139RSL is a novel endocytic motif and a structural element for clathrin-mediated nephrin endocytosis that functions as a phosphorylation-sensitive signal. We observed that Y1139RSL motif–mediated endocytosis helps to localize nephrin to specialized plasma membrane domains in podocytes and is essential for normal foot process organization into a functional slit diaphragm between neighboring foot processes in zebrafish. The importance of nephrin Y1139RSL for healthy podocyte development was supported by population-level analyses of genetic variations at this motif, revealing that such variations are very rare, suggesting that mutations in this motif have autosomal-recessive negative effects on kidney health. These findings expand our understanding of the mechanism underlying nephrin endocytosis and may lead to improved diagnostic tools or therapeutic strategies for managing early-onset, treatment-resistant nephrotic syndrome.

cell culture
cell adhesion
cell surface protein
cell-cell interaction
zebrafish
podocyte
nephrology
endocytosis
clathrin
clathrin-dependent endocytosis
foot processes
nephrin
nephrotic syndrome
slit diaphragm
kidney
glomerulus

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This work was supported by National Institutes of Health Grants T32DK061296 (to E. B. E.) and P30DK06010 and 1S10RR019003-01 (to N. A. H.), American Heart Association Grant 15GRNT25700019 (to A. S. U.), and NephCure Kidney International Grant 2012-RFE-003 (to A. S. U.). The authors declare that they have no conflicts of interest with the contents of this article. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

This article contains Figs. S1–S4.

1

Present address: Dept. of Nephrology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.

3

The abbreviations used are:

    CAM

    cell adhesion molecule

    NS

    nephrotic syndrome

    AP-2

    assembly polypeptide-2

    CCV

    clathrin-coated vesicle

    CCP

    clathrin-coated pit

    MO

    morpholino

    SPIM

    single-plane illumination microscopy

    TEM

    transmission electron microscopy

    dpf

    days postfertilization

    MUSCLE

    multisequence alignment with high accuracy and high throughput

    CD2AP

    CD2-associated protein

    WES

    whole exome

    WEG

    whole genome

    hs- and dr-

    human and zebrafish, respectively

    WCL

    whole-cell lysate

    BA

    Buffer A

    PM

    plasma membrane.