Notch Signaling in Nestin-Expressing Cells in the Bone Marrow Maintains Erythropoiesis via Macrophage Integrity.
Animals
Bone Marrow
/ metabolism
Bone Marrow Cells
/ metabolism
Cell Lineage
/ genetics
Erythropoiesis
/ genetics
Gene Expression Regulation
Genes, Reporter
Green Fluorescent Proteins
/ genetics
Interleukin-6
/ genetics
Macrophages
/ metabolism
Mice
Mice, Inbred C57BL
Mice, Transgenic
Nestin
/ genetics
Receptors, Notch
/ deficiency
Signal Transduction
Splenomegaly
/ genetics
Stem Cell Niche
/ genetics
Bone marrow stromal cells
Erythroid differentiation
Erythropoiesis
Nestin
Notch
Journal
Stem cells (Dayton, Ohio)
ISSN: 1549-4918
Titre abrégé: Stem Cells
Pays: England
ID NLM: 9304532
Informations de publication
Date de publication:
07 2019
07 2019
Historique:
received:
27
09
2018
revised:
12
03
2019
accepted:
21
03
2019
pubmed:
2
4
2019
medline:
27
6
2020
entrez:
2
4
2019
Statut:
ppublish
Résumé
Notch signaling plays pivotal roles in both hematopoietic stem/progenitor and their niche cells. Myeloproliferative phenotypes are induced by disruption of Notch signaling in nonhematopoietic bone marrow (BM) cells. Nestin-expressing cells in the BM reportedly represent a component of the hematopoietic stem cell niche. We established mice in which rare Nestin-expressing cells in the BM were marked by green fluorescent protein, and Notch signaling was conditionally disrupted in these cells specifically. We observed impairment of erythropoiesis in the BM accompanying splenomegaly with BM hematopoietic programs in other lineages undisturbed. Transplantation experiments revealed that the microenvironmental rather than the hematopoietic cells were attributable to these phenotypes. We further found that the erythroid-island-forming ability of BM central macrophages was compromised along with the transcriptional upregulation of interleukin-6. Various Inflammatory conditions hamper BM erythropoiesis, which often accompanies extramedullary hematopoiesis. The mouse model demonstrated here may be of relevance to this common pathophysiologic condition. Stem Cells 2019;37:924-936.
Substances chimiques
Interleukin-6
0
Nes protein, mouse
0
Nestin
0
Receptors, Notch
0
interleukin-6, mouse
0
Green Fluorescent Proteins
147336-22-9
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
924-936Informations de copyright
©AlphaMed Press 2019.