Universal fibroblasts across tissues can differentiate into niche cells for hematopoietic stem cells

Hematopoietic stem cells (HSCs) generating all blood cells are maintained by their niche cells, termed CXCL12-abundant reticular (CAR) cells, which strongly overlap with leptin-receptor-expressing (LepR<sup>+</sup>) cells in the bone marrow. A meta-analysis of single-cell RNA sequencing datasets across tissues hypothesized that universal fibroblasts present in all organs give rise to distinct tissue-specific fibroblast subsets designated as specialized fibroblasts, including CAR/LepR<sup>+</sup> cells. However, there is no direct evidence that universal fibroblasts can differentiate into specialized fibroblasts at a distant location. Here, we demonstrated that CD248<sup>+</sup> universal fibroblasts from the lung and colon outside the skeletal system, as well as from muscle, generated CAR/LepR<sup>+</sup> cells characterized by HSC niche functions and expression of cytokines and transcription factors essential for HSC maintenance during ectopic bone formation or after intra-bone marrow transplantation. These results demonstrate that universal fibroblasts with the potential to differentiate into bone marrow-specific HSC niche cells are scattered throughout the entire body.

Authors

Institutions

Publication Details

Journal
Cell Reports
Published
2025-05-01
DOI
https://doi.org/10.1016/j.celrep.2025.115620
Citations
4
Primary Topic
Hematopoietic Stem Cell Transplantation
Type
article
Field-Weighted Citation Impact
7.08
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Universal fibroblasts across tissues can differentiate into niche cells for hematopoietic stem cells

Yoshiki Omatsu, Shota Aiba, Kei Higaki, Takashi Nagasawa et al.
4 citations
Cell Reports
Hematopoietic Stem Cell Transplantation
7.08
article

Universal fibroblasts across tissues can differentiate into niche cells for hematopoietic stem cells

Yoshiki Omatsu, Shota Aiba, Kei Higaki, Takashi Nagasawa, Takashi Shimoyama
article en
4 citations

Abstract

Hematopoietic stem cells (HSCs) generating all blood cells are maintained by their niche cells, termed CXCL12-abundant reticular (CAR) cells, which strongly overlap with leptin-receptor-expressing (LepR<sup>+</sup>) cells in the bone marrow. A meta-analysis of single-cell RNA sequencing datasets across tissues hypothesized that universal fibroblasts present in all organs give rise to distinct tissue-specific fibroblast subsets designated as specialized fibroblasts, including CAR/LepR<sup>+</sup> cells. However, there is no direct evidence that universal fibroblasts can differentiate into specialized fibroblasts at a distant location. Here, we demonstrated that CD248<sup>+</sup> universal fibroblasts from the lung and colon outside the skeletal system, as well as from muscle, generated CAR/LepR<sup>+</sup> cells characterized by HSC niche functions and expression of cytokines and transcription factors essential for HSC maintenance during ectopic bone formation or after intra-bone marrow transplantation. These results demonstrate that universal fibroblasts with the potential to differentiate into bone marrow-specific HSC niche cells are scattered throughout the entire body.

Cell ReportsVol. 44(5)
Ube Frontier University (JP), The University of Osaka (JP)
Zero hunger
Openalex Percentile: Top 3%
Hematopoietic Stem Cell Transplantation
7.08
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.

Universal fibroblasts across tissues can differentiate into niche cells for hematopoietic stem cells — Yoshiki Omatsu, Shota Aiba, et al. · Cell Reports (2025) | TGRS Research Map | TGRS