Your browser doesn't support javascript.
loading
Ultrabright plasmonic fluor nanolabel-enabled detection of a urinary ER stress biomarker in autosomal dominant tubulointerstitial kidney disease.
Kim, Yeawon; Wang, Zheyu; Li, Chuang; Kidd, Kendrah; Wang, Yixuan; Johnson, Bryce G; Kmoch, Stanislav; Morrissey, Jeremiah J; Bleyer, Anthony J; Duffield, Jeremy S; Singamaneni, Srikanth; Chen, Ying Maggie.
Afiliación
  • Kim Y; Division of Nephrology, Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri.
  • Wang Z; Department of Mechanical Engineering and Materials Science, Institute of Materials Science and Engineering, Washington University in St. Louis, St. Louis, Missouri.
  • Li C; Division of Nephrology, Department of Internal Medicine, Washington University School of Medicine, St. Louis, Missouri.
  • Kidd K; Section of Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Wang Y; Research Unit of Rare Diseases, Department of Pediatric and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Johnson BG; Department of Mechanical Engineering and Materials Science, Institute of Materials Science and Engineering, Washington University in St. Louis, St. Louis, Missouri.
  • Kmoch S; Pfizer Worldwide Research and Development, Inflammation & Immunology, Cambridge, Massachusetts.
  • Morrissey JJ; Section of Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Bleyer AJ; Research Unit of Rare Diseases, Department of Pediatric and Adolescent Medicine, First Faculty of Medicine, Charles University, Prague, Czech Republic.
  • Duffield JS; Division of Clinical and Translational Research, Department of Anesthesiology, Washington University in St. Louis, St. Louis, Missouri.
  • Singamaneni S; Siteman Cancer Center, Washington University in St. Louis, St. Louis, Missouri.
  • Chen YM; Section of Nephrology, Wake Forest School of Medicine, Winston-Salem, North Carolina.
Am J Physiol Renal Physiol ; 321(2): F236-F244, 2021 08 01.
Article en En | MEDLINE | ID: mdl-34251273
ABSTRACT
Autosomal dominant tubulointerstitial kidney disease (ADTKD)-uromodulin (UMOD) is the most common nonpolycystic genetic kidney disease, but it remains unrecognized due to its clinical heterogeneity and lack of screening test. Moreover, the fact that the clinical feature is a poor predictor of disease outcome further highlights the need for the development of mechanistic biomarkers in ADTKD. However, low abundant urinary proteins secreted by thick ascending limb cells, where UMOD is synthesized, have posed a challenge for the detection of biomarkers in ADTKD-UMOD. In the CRISPR/Cas9-generated murine model and patients with ADTKD-UMOD, we found that immunoglobulin heavy chain-binding protein (BiP), an endoplasmic reticulum chaperone, was exclusively upregulated by mutant UMOD in the thick ascending limb and easily detected by Western blot analysis in the urine at an early stage of disease. However, even the most sensitive ELISA failed to detect urinary BiP in affected individuals. We therefore developed an ultrasensitive, plasmon-enhanced fluorescence-linked immunosorbent assay (p-FLISA) to quantify urinary BiP concentration by harnessing the newly invented ultrabright fluorescent nanoconstruct, termed "plasmonic Fluor." p-FLISA demonstrated that urinary BiP excretion was significantly elevated in patients with ADTKD-UMOD compared with unaffected controls, which may have potential utility in risk stratification, disease activity monitoring, disease progression prediction, and guidance of endoplasmic reticulum-targeted therapies in ADTKD.NEW & NOTEWORTHY Autosomal dominant tubulointerstitial kidney disease (ADTKD)-uromodulin (UMOD) is an underdiagnosed cause of chronic kidney disease (CKD). Lack of ultrasensitive bioanalytical tools has hindered the discovery of low abundant urinary biomarkers in ADTKD. Here, we developed an ultrasensitive plasmon-enhanced fluorescence-linked immunosorbent assay (p-FLISA). p-FLISA demonstrated that secreted immunoglobulin heavy chain-binding protein is an early urinary endoplasmic reticulum stress biomarker in ADTKD-UMOD, which will be valuable in monitoring disease progression and the treatment response in ADTKD.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biomarcadores / Técnicas de Inmunoadsorción / Estrés del Retículo Endoplásmico / Proteínas de Choque Térmico / Nefritis Intersticial Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Am J Physiol Renal Physiol Asunto de la revista: FISIOLOGIA / NEFROLOGIA Año: 2021 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Biomarcadores / Técnicas de Inmunoadsorción / Estrés del Retículo Endoplásmico / Proteínas de Choque Térmico / Nefritis Intersticial Tipo de estudio: Diagnostic_studies / Guideline / Prognostic_studies Límite: Animals / Humans Idioma: En Revista: Am J Physiol Renal Physiol Asunto de la revista: FISIOLOGIA / NEFROLOGIA Año: 2021 Tipo del documento: Article