Bone marrow sinusoidal endothelium controls terminal erythroid differentiation and reticulocyte maturation

Joschka Heil(Heidelberg University), Victor Olsavszky(Heidelberg University), Katrin Busch(German Cancer Research Center), Kay Klapproth(German Cancer Research Center), Carolina De La Torre(Heidelberg University), Carsten Sticht(Heidelberg University), Kajetan Sandorski(Heidelberg University), Johannes Hoffmann(Heidelberg University), Hiltrud Schönhaber(Heidelberg University), Johanna Zierow(Heidelberg University), Manuel Winkler(Heidelberg University), Christian David Schmid(Heidelberg University), Theresa Staniczek(Heidelberg University), Deborah E. Daniels(University of Bristol), Jan Frayne(University of Bristol), Georgia Metzgeroth(Heidelberg University), Daniel Nowak(Heidelberg University), Sven Schneider(Heidelberg University), Michael Neumaier(Heidelberg University), Vanessa Weyer(Heidelberg University), Christoph Groden(Heidelberg University), Hermann‐Josef Gröne(Philipps University of Marburg), Karsten Richter(German Cancer Research Center), Carolin Mogler(Technical University of Munich), Makoto M. Taketo(Kyoto University), Kai Schledzewski(Heidelberg University), Cyrill Géraud(Heidelberg University), Sergij Goerdt(Heidelberg University), Philipp‐Sebastian Koch(Heidelberg University)
Nature Communications
November 29, 2021
Cited by 19Open Access
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Abstract

Abstract Within the bone marrow microenvironment, endothelial cells (EC) exert important functions. Arterial EC support hematopoiesis while H-type capillaries induce bone formation. Here, we show that BM sinusoidal EC (BM-SEC) actively control erythropoiesis. Mice with stabilized β-catenin in BM-SEC ( Ctnnb1 OE-SEC ) generated by using a BM-SEC-restricted Cre mouse line ( Stab2-iCreF3 ) develop fatal anemia. While activation of Wnt-signaling in BM-SEC causes an increase in erythroblast subsets (PII–PIV), mature erythroid cells (PV) are reduced indicating impairment of terminal erythroid differentiation/reticulocyte maturation. Transplantation of Ctnnb1 OE-SEC hematopoietic stem cells into wildtype recipients confirms lethal anemia to be caused by cell-extrinsic, endothelial-mediated effects. Ctnnb1 OE-SEC BM-SEC reveal aberrant sinusoidal differentiation with altered EC gene expression and perisinusoidal ECM deposition and angiocrine dysregulation with de novo endothelial expression of FGF23 and DKK2, elevated in anemia and involved in vascular stabilization, respectively. Our study demonstrates that BM-SEC play an important role in the bone marrow microenvironment in health and disease.


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