{"title":"通过单细胞综合分析,揭示与成年小鼠年龄相关性骨质疏松症有关的两种不同的骨胶质细胞群。","authors":"Bo Zhou, Hongwen Huang, Zhen Ding, Kaiwen Luo, Yangshan Chen, Yingying Han, Wei Pang, Wanze Tang, Litong Chen, Wenfei Jin, Guixing Ma, Huiling Cao","doi":"10.1007/s00018-025-05597-w","DOIUrl":null,"url":null,"abstract":"<p><p>The bone marrow microenvironment contains heterogeneous stromal cells, which are critical for bone remodeling and provide essential supportive roles for hematopoietic functions. Although the diversity of PDGFRα<sup>+</sup>β<sup>+</sup> mesenchymal stromal/stem cells (MSCs) get consensus, the osteo-lineage cells (OLCs) that constitute the developmental trajectory of osteoblasts are largely remain unclear. Here, we construct a comprehensive atlas of stromal cell via performing integrative single cell analyses for 77 samples from 14 datasets. Besides previously defined Lepr<sup>+</sup> BM-MSCs derived OLC1, we present a novel OLC2 with unique molecular signatures and differentiation pathway. Both OLC1 and OLC2 show significant polygenic association with bone mineral density (BMD), while extracellular matrix (ECM) proteins specifically expressed by OLC2 are particularly decreased in bone tissue of aged mice. Notably, OLC1 and OLC2 are consistently reduced in aged mice, which might be induced by the decreased expression of several lineage drivers. Collectively, our study presents a thorough prospect of OLCs in the bone marrow microenvironment and highlights their important roles in age-related osteoporosis.</p>","PeriodicalId":10007,"journal":{"name":"Cellular and Molecular Life Sciences","volume":"82 1","pages":"106"},"PeriodicalIF":6.2000,"publicationDate":"2025-03-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11896952/pdf/","citationCount":"0","resultStr":"{\"title\":\"Unveiling two distinct osteolineage cell populations linked to age-related osteoporosis in adult mice through integrative single-cell analyses.\",\"authors\":\"Bo Zhou, Hongwen Huang, Zhen Ding, Kaiwen Luo, Yangshan Chen, Yingying Han, Wei Pang, Wanze Tang, Litong Chen, Wenfei Jin, Guixing Ma, Huiling Cao\",\"doi\":\"10.1007/s00018-025-05597-w\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The bone marrow microenvironment contains heterogeneous stromal cells, which are critical for bone remodeling and provide essential supportive roles for hematopoietic functions. Although the diversity of PDGFRα<sup>+</sup>β<sup>+</sup> mesenchymal stromal/stem cells (MSCs) get consensus, the osteo-lineage cells (OLCs) that constitute the developmental trajectory of osteoblasts are largely remain unclear. Here, we construct a comprehensive atlas of stromal cell via performing integrative single cell analyses for 77 samples from 14 datasets. Besides previously defined Lepr<sup>+</sup> BM-MSCs derived OLC1, we present a novel OLC2 with unique molecular signatures and differentiation pathway. Both OLC1 and OLC2 show significant polygenic association with bone mineral density (BMD), while extracellular matrix (ECM) proteins specifically expressed by OLC2 are particularly decreased in bone tissue of aged mice. Notably, OLC1 and OLC2 are consistently reduced in aged mice, which might be induced by the decreased expression of several lineage drivers. Collectively, our study presents a thorough prospect of OLCs in the bone marrow microenvironment and highlights their important roles in age-related osteoporosis.</p>\",\"PeriodicalId\":10007,\"journal\":{\"name\":\"Cellular and Molecular Life Sciences\",\"volume\":\"82 1\",\"pages\":\"106\"},\"PeriodicalIF\":6.2000,\"publicationDate\":\"2025-03-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11896952/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cellular and Molecular Life Sciences\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1007/s00018-025-05597-w\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMISTRY & MOLECULAR BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cellular and Molecular Life Sciences","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1007/s00018-025-05597-w","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
Unveiling two distinct osteolineage cell populations linked to age-related osteoporosis in adult mice through integrative single-cell analyses.
The bone marrow microenvironment contains heterogeneous stromal cells, which are critical for bone remodeling and provide essential supportive roles for hematopoietic functions. Although the diversity of PDGFRα+β+ mesenchymal stromal/stem cells (MSCs) get consensus, the osteo-lineage cells (OLCs) that constitute the developmental trajectory of osteoblasts are largely remain unclear. Here, we construct a comprehensive atlas of stromal cell via performing integrative single cell analyses for 77 samples from 14 datasets. Besides previously defined Lepr+ BM-MSCs derived OLC1, we present a novel OLC2 with unique molecular signatures and differentiation pathway. Both OLC1 and OLC2 show significant polygenic association with bone mineral density (BMD), while extracellular matrix (ECM) proteins specifically expressed by OLC2 are particularly decreased in bone tissue of aged mice. Notably, OLC1 and OLC2 are consistently reduced in aged mice, which might be induced by the decreased expression of several lineage drivers. Collectively, our study presents a thorough prospect of OLCs in the bone marrow microenvironment and highlights their important roles in age-related osteoporosis.
期刊介绍:
Journal Name: Cellular and Molecular Life Sciences (CMLS)
Location: Basel, Switzerland
Focus:
Multidisciplinary journal
Publishes research articles, reviews, multi-author reviews, and visions & reflections articles
Coverage:
Latest aspects of biological and biomedical research
Areas include:
Biochemistry and molecular biology
Cell biology
Molecular and cellular aspects of biomedicine
Neuroscience
Pharmacology
Immunology
Additional Features:
Welcomes comments on any article published in CMLS
Accepts suggestions for topics to be covered