Elevated granulocyte-colony stimulating factor and hematopoietic stem cell mobilization in Niemann-Pick type C1 disease.
J Lipid Res
; 63(2): 100167, 2022 02.
Article
en En
| MEDLINE
| ID: mdl-35007562
ABSTRACT
Niemann-Pick type C1 (NPC1) disease is a progressive lysosomal storage disorder caused by mutations of the NPC1 gene. While neurodegeneration is the most severe symptom, a large proportion of NPC1 patients also present with splenomegaly, which has been attributed to cholesterol and glycosphingolipid accumulation in late endosomes and lysosomes. However, recent data also reveal an increase in the inflammatory monocyte subset in the Npc1nih mouse model expressing an Npc1 null allele. We evaluated the contribution of hematopoietic cells to splenomegaly in NPC1 disease under conditions of hypercholesterolemia. We transplanted Npc1nih (Npc1 null mutation) or Npc1wt bone marrow (BM) into Ldlr-/- mice and fed these mice a cholesterol-rich Western-type diet. At 9 weeks after BM transplant, on a chow diet, the Npc1 null mutation increased plasma granulocyte-colony stimulating factor (G-CSF) by 2-fold and caused mild neutrophilia. At 18 weeks after BM transplant, including 9 weeks of Western-type diet feeding, the Npc1 mutation increased G-csf mRNA levels by â¼5-fold in splenic monocytes/macrophages accompanied by a â¼4-fold increase in splenic neutrophils compared with controls. We also observed â¼5-fold increased long-term and short-term hematopoietic stem cells (HSCs) in the spleen, and a â¼30-75% decrease of these populations in BM, reflecting HSC mobilization, presumably downstream of elevated G-CSF. In line with these data, four patients with NPC1 disease showed higher plasma G-CSF compared with age-matched and gender-matched healthy controls. In conclusion, we show elevated G-CSF levels and HSC mobilization in the setting of an Npc1 null mutation and propose that this contributes to splenomegaly in patients with NPC1 disease.
Palabras clave
Texto completo:
1
Banco de datos:
MEDLINE
Asunto principal:
Movilización de Célula Madre Hematopoyética
Tipo de estudio:
Prognostic_studies
Idioma:
En
Revista:
J Lipid Res
Año:
2022
Tipo del documento:
Article
País de afiliación:
Países Bajos