An adipo-osteoprogenitor population in the endosteal niche contributes to bone and fat formation in adult mouse bone marrow

X Xueyang Liao (Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia) J Jasmin Koehnken Sawall (Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia) R Rebecca Seeley (Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia) F Fangfang Song (Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia) X Xing Ji (Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia) X Xiaobin Liu (Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia) C Chao Song F Fanxin Long (Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia)

Abstract

The adult bone marrow houses progenitors for both osteoblasts and adipocytes, but their precise molecular identity remains to be fully elucidated. Previous studies indicate that Lepr + Cxcl12 + bone marrow stromal cells collectively give rise to both osteoblasts and marrow adipocytes, but the high degree of heterogeneity among those cells calls for further delineation of common or lineage-specific progenitors in vivo. Here, by single-cell RNA-sequencing we identify a small subset of bone marrow stromal cells coexpressing Adipoq and Osx, along with other osteogenic or adipogenic genes. The Adipoq + Osx + cells predominantly reside in the endosteal niche. Intersectional genetic fate mapping with Dre and Cre recombinases demonstrates dual differentiation of osteoblasts and adipocytes from the Adipoq + Osx + cells in vivo. The data support the Adipoq + Osx + cells as adipo-osteoprogenitors contributing to bone and fat formation in the adult mouse bone marrow.

Article Details

Volume / Issue Vol. 122, Issue 47
Published November 25, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (8)

X

Xueyang Liao

Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia

J

Jasmin Koehnken Sawall

Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia

R

Rebecca Seeley

Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia

F

Fangfang Song

Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia

X

Xing Ji

Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia

X

Xiaobin Liu

Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia

C

Chao Song

F

Fanxin Long

Department of Surgery, Translational Research Program in Pediatric Orthopedics, The Children’s Hospital of Philadelphia