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Single-cell RNA-seq of rheumatoid arthritis synovial tissue using low-cost microfluidic instrumentation.
Stephenson, William; Donlin, Laura T; Butler, Andrew; Rozo, Cristina; Bracken, Bernadette; Rashidfarrokhi, Ali; Goodman, Susan M; Ivashkiv, Lionel B; Bykerk, Vivian P; Orange, Dana E; Darnell, Robert B; Swerdlow, Harold P; Satija, Rahul.
Afiliación
  • Stephenson W; Technology Innovation Lab, New York Genome Center, New York, NY, 10013, USA. wstephenson@nygenome.org.
  • Donlin LT; Hospital for Special Surgery, New York, NY, 10021, USA.
  • Butler A; Weill Cornell Medical College, New York, NY, 10065, USA.
  • Rozo C; New York Genome Center, New York, NY, 10013, USA.
  • Bracken B; New York University, Center for Genomics and Systems Biology, New York, NY, 10003, USA.
  • Rashidfarrokhi A; Hospital for Special Surgery, New York, NY, 10021, USA.
  • Goodman SM; New York Genome Center, New York, NY, 10013, USA.
  • Ivashkiv LB; New York University, Center for Genomics and Systems Biology, New York, NY, 10003, USA.
  • Bykerk VP; New York Genome Center, New York, NY, 10013, USA.
  • Orange DE; New York University School of Medicine, New York, NY, 10016, USA.
  • Darnell RB; Hospital for Special Surgery, New York, NY, 10021, USA.
  • Swerdlow HP; Weill Cornell Medical College, New York, NY, 10065, USA.
  • Satija R; Hospital for Special Surgery, New York, NY, 10021, USA.
Nat Commun ; 9(1): 791, 2018 02 23.
Article en En | MEDLINE | ID: mdl-29476078
ABSTRACT
Droplet-based single-cell RNA-seq has emerged as a powerful technique for massively parallel cellular profiling. While this approach offers the exciting promise to deconvolute cellular heterogeneity in diseased tissues, the lack of cost-effective and user-friendly instrumentation has hindered widespread adoption of droplet microfluidic techniques. To address this, we developed a 3D-printed, low-cost droplet microfluidic control instrument and deploy it in a clinical environment to perform single-cell transcriptome profiling of disaggregated synovial tissue from five rheumatoid arthritis patients. We sequence 20,387 single cells revealing 13 transcriptomically distinct clusters. These encompass an unsupervised draft atlas of the autoimmune infiltrate that contribute to disease biology. Additionally, we identify previously uncharacterized fibroblast subpopulations and discern their spatial location within the synovium. We envision that this instrument will have broad utility in both research and clinical settings, enabling low-cost and routine application of microfluidic techniques.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Artritis Reumatoide / ARN / Microfluídica / Análisis de la Célula Individual Tipo de estudio: Evaluation_studies / Health_economic_evaluation Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Artritis Reumatoide / ARN / Microfluídica / Análisis de la Célula Individual Tipo de estudio: Evaluation_studies / Health_economic_evaluation Límite: Humans Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2018 Tipo del documento: Article País de afiliación: Estados Unidos