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Recessive missense LAMP3 variant associated with defect in lamellar body biogenesis and fatal neonatal interstitial lung disease in dogs.
Dillard, Kati J; Ochs, Matthias; Niskanen, Julia E; Arumilli, Meharji; Donner, Jonas; Kyöstilä, Kaisa; Hytönen, Marjo K; Anttila, Marjukka; Lohi, Hannes.
Afiliación
  • Dillard KJ; Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland.
  • Ochs M; Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.
  • Niskanen JE; Folkhälsan Research Center, Helsinki, Finland.
  • Arumilli M; Veterinary Bacteriology and Pathology Research Unit, Finnish Food Authority, Helsinki, Finland.
  • Donner J; Institute of Functional and Applied Anatomy, Hannover Medical School, Hannover, Germany.
  • Kyöstilä K; Institute of Functional Anatomy, Charité - Universitaetsmedizin Berlin, Berlin, Germany.
  • Hytönen MK; German Center for Lung Research (DZL), Berlin, Germany.
  • Anttila M; Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland.
  • Lohi H; Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.
PLoS Genet ; 16(3): e1008651, 2020 03.
Article en En | MEDLINE | ID: mdl-32150563
Neonatal interstitial lung diseases due to abnormal surfactant biogenesis are rare in humans and have never been reported as a spontaneous disorder in animals. We describe here a novel lung disorder in Airedale Terrier (AT) dogs with clinical symptoms and pathology similar to the most severe neonatal forms of human surfactant deficiency. Lethal hypoxic respiratory distress and failure occurred within the first days or weeks of life in the affected puppies. Transmission electron microscopy of the affected lungs revealed maturation arrest in the formation of lamellar bodies (LBs) in the alveolar epithelial type II (AECII) cells. The secretory organelles were small and contained fewer lamellae, often in combination with small vesicles surrounded by an occasionally disrupted common limiting membrane. A combined approach of genome-wide association study and whole exome sequencing identified a recessive variant, c.1159G>A, p.(E387K), in LAMP3, a limiting membrane protein of the cytoplasmic surfactant organelles in AECII cells. The substitution resides in the LAMP domain adjacent to a conserved disulfide bond. In summary, this study describes a novel interstitial lung disease in dogs, identifies a new candidate gene for human surfactant dysfunction and brings important insights into the essential role of LAMP3 in the process of the LB formation.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Pulmonares Intersticiales / Proteína 3 de la Membrana Asociada a Lisosoma Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2020 Tipo del documento: Article País de afiliación: Finlandia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Enfermedades Pulmonares Intersticiales / Proteína 3 de la Membrana Asociada a Lisosoma Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: En Revista: PLoS Genet Asunto de la revista: GENETICA Año: 2020 Tipo del documento: Article País de afiliación: Finlandia