A Phenotypic Screening Assay Identifies Modulators of Diamond Blackfan Anemia.


Journal

SLAS discovery : advancing life sciences R & D
ISSN: 2472-5560
Titre abrégé: SLAS Discov
Pays: United States
ID NLM: 101697563

Informations de publication

Date de publication:
03 2019
Historique:
entrez: 21 2 2019
pubmed: 21 2 2019
medline: 6 5 2020
Statut: ppublish

Résumé

Diamond-Blackfan anemia (DBA) is a bone marrow failure syndrome caused by mutations in ribosomal protein genes. Pathogenic mechanisms are poorly understood but involve severely reduced proliferation of erythroid precursors. Because current DBA therapies are ineffective and associated with severe side effects, disease-specific therapies are urgently needed. We hypothesized that druggable molecular pathways underlying the defect can be revealed through phenotypic small-molecule screens. Accordingly, a screening assay was developed using c-kit+ fetal liver erythroid progenitors from a doxycycline-inducible DBA mouse model. The addition of doxycycline to the culture medium induces the phenotype and reduces proliferation to <10% of normal, such that rescue of proliferation can be used as a simple readout for screening. Here, we describe the assay rationale and efforts toward validation of a microtiter plate-compatible assay and its application in a pilot screen of 3871 annotated compounds. Ten hits demonstrated concentration-dependent activity, and we report a brief follow-up of one of these compounds. In conclusion, we established a robust scalable assay for screening molecules that rescue erythropoiesis in DBA.

Identifiants

pubmed: 30784369
doi: 10.1177/2472555218823531
pii: S2472-5552(22)12619-5
doi:

Substances chimiques

Doxycycline N12000U13O

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

304-313

Auteurs

Kavitha Siva (K)

1 Department of Molecular Medicine and Gene Therapy, Lund Strategic Center for Stem Cell Biology, Lund University, Lund, Sweden.

Fredrik Ek (F)

2 Chemical Biology and Therapeutics group, Department of Experimental Medical Science, Lund University, Lund, Sweden.

Jun Chen (J)

1 Department of Molecular Medicine and Gene Therapy, Lund Strategic Center for Stem Cell Biology, Lund University, Lund, Sweden.

Abdul Ghani Alattar (A)

1 Department of Molecular Medicine and Gene Therapy, Lund Strategic Center for Stem Cell Biology, Lund University, Lund, Sweden.

Kristmundur Sigmundsson (K)

3 Chemical Biology Consortium Sweden (CBCS), Science for Life Laboratory, Department for Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Solna, Sweden.

Roger Olsson (R)

2 Chemical Biology and Therapeutics group, Department of Experimental Medical Science, Lund University, Lund, Sweden.

Marcin Wlodarski (M)

4 Division of Pediatric Hematology and Oncology, Faculty of Medicine University Hospital Freiburg, Germany.

Thomas Lundbäck (T)

3 Chemical Biology Consortium Sweden (CBCS), Science for Life Laboratory, Department for Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Solna, Sweden.
5 Mechanistic Biology & Profiling, Discovery Sciences, IMED Biotech Unit, AstraZeneca, Gothenburg, Sweden.

Johan Flygare (J)

1 Department of Molecular Medicine and Gene Therapy, Lund Strategic Center for Stem Cell Biology, Lund University, Lund, Sweden.

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Classifications MeSH