Effect of the LSD1 inhibitor RN-1 on γ-globin and global gene expression during erythroid differentiation in baboons (Papio anubis)

• Published in: PloS one Vol. 18; no. 12; p. e0289860
• Main Authors: Ibanez, Vinzon, Vaitkus, Kestis, Ruiz, Maria Armila, Lei, Zhengdeng, Maienschein-Cline, Mark, Arbieva, Zarema, Lavelle, Donald
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 01-12-2023; Public Library of Science (PLoS)
• Subjects: Accreditation; Anemia; Anemia, Sickle Cell - genetics; Animal models; Animal welfare; Animals; Baboons; Bone marrow; Cell differentiation; Clinical trials; Differentiation; Drug dosages; Enzymes; Epigenetics; Erythroid cells; Fetal Hemoglobin - genetics; Fetuses; Food; Fruits; gamma-Globins - genetics; Gene deletion; Gene Expression; Gene silencing; Genes; Hemoglobin; Histone Demethylases - antagonists & inhibitors; Humans; In vivo methods and tests; Inhibitors; Laboratory animals; Lysine; Mice; Monkeys & apes; Papio anubis; Papio anubis - genetics; Primates; Sickle cell disease; Signs and symptoms; Subpopulations; Transcriptomes
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0289860

Elevated levels of Fetal Hemoglobin interfere with polymerization of sickle hemoglobin thereby reducing anemia, lessening the severity of symptoms, and increasing life span of patients with sickle cell disease. An affordable, small molecule drug that stimulates HbF expression in vivo would be ideally suited to treat the large numbers of SCD patients that exist worldwide. Our previous work showed that administration of the LSD1 (KDM1A) inhibitor RN-1 to normal baboons increased Fetal Hemoglobin (HbF) and was tolerated over a prolonged treatment period. HbF elevations were associated with changes in epigenetic modifications that included increased levels of H3K4 di-and tri-methyl lysine at the γ-globin promoter. While dramatic effects of the loss of LSD1 on hematopoietic differentiation have been observed in murine LSD1 gene deletion and silencing models, the effect of pharmacological inhibition of LSD1 in vivo on hematopoietic differentiation is unknown. The goal of these experiments was to investigate the in vivo mechanism of action of the LSD1 inhibitor RN-1 by determining its effect on γ-globin expression in highly purified subpopulations of bone marrow erythroid cells enriched for varying stages of erythroid differentiation isolated directly from baboons treated with RN-1 and also by investigating the effect of RN1 on the global transcriptome in a highly purified population of proerythroblasts. Our results show that RN-1 administered to baboons targets an early event during erythroid differentiation responsible for γ-globin repression and increases the expression of a limited number of genes including genes involved in erythroid differentiation such as GATA2, GFi-1B, and LYN.