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Automated detection and quantification of Wilms' Tumor 1-positive cells in murine diabetic kidney disease.
Govind, Darshana; Santo, Briana A; Ginley, Brandon; Yacoub, Rabi; Rosenberg, Avi Z; Jen, Kuang-Yu; Walavalkar, Vignesh; Wilding, Gregory E; Worral, Amber M; Mohammad, Imtiaz; Sarder, Pinaki.
Afiliação
  • Govind D; Department of Pathology and Anatomical Sciences, University at Buffalo, Buffalo, NY.
  • Santo BA; Department of Pathology and Anatomical Sciences, University at Buffalo, Buffalo, NY.
  • Ginley B; Department of Pathology and Anatomical Sciences, University at Buffalo, Buffalo, NY.
  • Yacoub R; Department of Internal Medicine, University at Buffalo, Buffalo, NY.
  • Rosenberg AZ; Department of Pathology, Johns Hopkins University School of Medicine, Baltimore, MD.
  • Jen KY; Department of Pathology and Laboratory Medicine, University of California at Davis, CA.
  • Walavalkar V; Department of Pathology, University of California San Francisco, San Francisco, CA.
  • Wilding GE; Department of Biostatistics, University at Buffalo, Buffalo, NY.
  • Worral AM; Department of Pathology and Anatomical Sciences, University at Buffalo, Buffalo, NY.
  • Mohammad I; Department of Pathology and Anatomical Sciences, University at Buffalo, Buffalo, NY.
  • Sarder P; Department of Pathology and Anatomical Sciences, University at Buffalo, Buffalo, NY.
Article em En | MEDLINE | ID: mdl-34366543
ABSTRACT
In diabetic kidney disease (DKD), podocyte depletion, and the subsequent migration of parietal epithelial cells (PECs) to the tuft, is a precursor to progressive glomerular damage, but the limitations of brightfield microscopy currently preclude direct pathological quantitation of these cells. Here we present an automated approach to podocyte and PEC detection developed using kidney sections from mouse model emulating DKD, stained first for Wilms' Tumor 1 (WT1) (podocyte and PEC marker) by immunofluorescence, then post-stained with periodic acid-Schiff (PAS). A generative adversarial network (GAN)-based pipeline was used to translate these PAS-stained sections into WT1-labeled IF images, enabling in silico label-free podocyte and PEC identification in brightfield images. Our method detected WT1-positive cells with high sensitivity/specificity (0.87/0.92). Additionally, our algorithm performed with a higher Cohen's kappa (0.85) than the average manual identification by three renal pathologists (0.78). We propose that this pipeline will enable accurate detection of WT1-positive cells in research applications.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Proc SPIE Int Soc Opt Eng Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Diagnostic_studies Idioma: En Revista: Proc SPIE Int Soc Opt Eng Ano de publicação: 2021 Tipo de documento: Article