{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T10:44:16Z","timestamp":1791283456972,"version":"4.1.0"},"reference-count":37,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"12","funder":[{"DOI":"10.13039\/501100001659","name":"Deutsche Forschungsgemeinschaft","doi-asserted-by":"publisher","award":["HE 7456\/3-1"],"award-info":[{"award-number":["HE 7456\/3-1"]}],"id":[{"id":"10.13039\/501100001659","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["RC2-DK122397"],"award-info":[{"award-number":["RC2-DK122397"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100004543","name":"China Scholarship Council","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100004543","id-type":"DOI","asserted-by":"publisher"}]},{"name":"Deutsche Gesellschaft f\u00fcr Innere Medizin"},{"DOI":"10.13039\/501100002714","name":"University of Freiburg","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100002714","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":["JASN"],"published-print":{"date-parts":[[2022,12]]},"abstract":"<jats:sec>\n                    <jats:title>Background<\/jats:title>\n                    <jats:p>\n                      Variants in\n                      <jats:italic toggle=\"yes\">TBC1D8B<\/jats:italic>\n                      cause nephrotic syndrome. TBC1D8B is a GTPase-activating protein for Rab11 (RAB11-GAP) that interacts with nephrin, but how it controls nephrin trafficking or other podocyte functions remains unclear.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Methods<\/jats:title>\n                    <jats:p>\n                      We generated a stable deletion in\n                      <jats:italic toggle=\"yes\">Tbc1d8b<\/jats:italic>\n                      and used microhomology-mediated end-joining for genome editing.\n                      <jats:italic toggle=\"yes\">Ex vivo<\/jats:italic>\n                      functional assays utilized slit diaphragms in podocyte-like\n                      <jats:italic toggle=\"yes\">Drosophila<\/jats:italic>\n                      nephrocytes. Manipulation of endocytic regulators and transgenesis of murine\n                      <jats:italic toggle=\"yes\">Tbc1d8b<\/jats:italic>\n                      provided a comprehensive functional analysis of Tbc1d8b.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results<\/jats:title>\n                    <jats:p>\n                      A null allele of\n                      <jats:italic toggle=\"yes\">Drosophila TBC1D8B<\/jats:italic>\n                      exhibited a nephrocyte-restricted phenotype of nephrin mislocalization, similar to patients with isolated nephrotic syndrome who have variants in the gene. The protein was required for rapid nephrin turnover in nephrocytes and for endocytosis of nephrin induced by excessive Rab5 activity. The protein expressed from the\n                      <jats:italic toggle=\"yes\">Tbc1d8b<\/jats:italic>\n                      locus bearing the edited tag predominantly localized to mature early and late endosomes. Tbc1d8b was required for endocytic cargo processing and degradation. Silencing\n                      <jats:italic toggle=\"yes\">Hrs<\/jats:italic>\n                      , a regulator of endosomal maturation, phenocopied loss of\n                      <jats:italic toggle=\"yes\">Tbc1d8b<\/jats:italic>\n                      . Low-level expression of murine\n                      <jats:italic toggle=\"yes\">TBC1D8B<\/jats:italic>\n                      rescued loss of the\n                      <jats:italic toggle=\"yes\">Drosophila<\/jats:italic>\n                      gene, indicating evolutionary conservation. Excessive murine TBC1D8B selectively disturbed nephrin dynamics. Finally, we discovered four novel\n                      <jats:italic toggle=\"yes\">TBC1D8B<\/jats:italic>\n                      variants within a cohort of 363 patients with FSGS and validated a functional effect of two variants in\n                      <jats:italic toggle=\"yes\">Drosophila,<\/jats:italic>\n                      suggesting a personalized platform for\n                      <jats:italic toggle=\"yes\">TBC1D8B<\/jats:italic>\n                      -associated FSGS.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusions<\/jats:title>\n                    <jats:p>\n                      Variants in\n                      <jats:italic toggle=\"yes\">TBC1D8B<\/jats:italic>\n                      are not infrequent among patients with FSGS. TBC1D8B, functioning in endosomal maturation and degradation, is essential for nephrin trafficking.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.1681\/asn.2022030275","type":"journal-article","created":{"date-parts":[[2022,9,22]],"date-time":"2022-09-22T15:35:14Z","timestamp":1663860914000},"page":"2174-2193","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":28,"title":["Nephrotic Syndrome Gene TBC1D8B Is Required for Endosomal Maturation and Nephrin Endocytosis in Drosophila"],"prefix":"10.1681","volume":"33","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-7653-0011","authenticated-orcid":false,"given":"Julian","family":"Milosavljevic","sequence":"first","affiliation":[{"name":"Renal Division, Department of Medicine, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, 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Medical Center, University of Freiburg, Freiburg, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Claire","family":"Leroy","sequence":"additional","affiliation":[{"name":"Renal Division, Department of Medicine, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mengmeng","family":"Chen","sequence":"additional","affiliation":[{"name":"Renal Division, Department of Medicine, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-9525-1288","authenticated-orcid":false,"given":"Lea","family":"Gerstner","sequence":"additional","affiliation":[{"name":"Renal Division, Department of Medicine, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dominik","family":"Spitz","sequence":"additional","affiliation":[{"name":"Renal Division, Department of Medicine, Faculty of Medicine and Medical Center, University of Freiburg, Freiburg, Germany"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Minxian","family":"Wang","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Beth Israel Deaconess Medical Center, Boston, Massachusetts"},{"name":"Department of Medicine, Harvard Medical School, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Andrea U.","family":"Knob","sequence":"additional","affiliation":[{"name":"Division of Nephrology, Beth Israel Deaconess Medical Center, Boston, Massachusetts"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"S\u00e9verine","family":"Kayser","sequence":"additional","affiliation":[{"name":"Renal Division, Department of Medicine, Faculty of 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