Hyaluronic acid–GPRC5C signalling promotes dormancy in haematopoietic stem cells

Author:

Zhang Yu Wei,Mess Julian,Aizarani Nadim,Mishra Pankaj,Johnson Carys,Romero-Mulero Mari Carmen,Rettkowski Jasmin,Schönberger Katharina,Obier Nadine,Jäcklein Karin,Woessner Nadine M.,Lalioti Maria-Eleni,Velasco-Hernandez Talia,Sikora Katarzyna,Wäsch Ralph,Lehnertz Bernhard,Sauvageau Guy,Manke Thomas,Menendez Pablo,Walter Sebastian Gottfried,Minguet Susana,Laurenti Elisa,Günther Stefan,Grün Dominic,Cabezas-Wallscheid NinaORCID

Abstract

AbstractBone marrow haematopoietic stem cells (HSCs) are vital for lifelong maintenance of healthy haematopoiesis. In inbred mice housed in gnotobiotic facilities, the top of the haematopoietic hierarchy is occupied by dormant HSCs, which reversibly exit quiescence during stress. Whether HSC dormancy exists in humans remains debatable. Here, using single-cell RNA sequencing, we show a continuous landscape of highly purified human bone marrow HSCs displaying varying degrees of dormancy. We identify the orphan receptor GPRC5C, which enriches for dormant human HSCs. GPRC5C is also essential for HSC function, as demonstrated by genetic loss- and gain-of-function analyses. Through structural modelling and biochemical assays, we show that hyaluronic acid, a bone marrow extracellular matrix component, preserves dormancy through GPRC5C. We identify the hyaluronic acid–GPRC5C signalling axis controlling the state of dormancy in mouse and human HSCs.

Funder

Max-Planck-Gesellschaft

Publisher

Springer Science and Business Media LLC

Subject

Cell Biology

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