Xiaohua Li
Current Organizations / Institutes
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Previous Organizations / Institutes
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Xiaohua Li has a total of 22 co-authors. Here are the top co-authors by number of shared publications:
Jianbo Li
Hunan University of Arts and Sciences
2 shared publicationsCui Zhou
Laboratory of Molecular and Statistical Genetics, College of Life Sciences, Hunan Normal University, Changsha, Hunan 410081, China
1 shared publication- Hong-Mei Xiao
Center for System Biology, Data Sciences, and Reproductive Health, School of Basic Medical Science, Central South University , 172 Tongzipo Road, Yuelu District, Changsha 410013, Hunan Province
1 shared publication - Hong-Wen Deng
School of Medicine, Tulane University, New Orleans, LA, USA
1 shared publication - Hui Shen
School of Medicine, Tulane University, New Orleans, LA, USA
1 shared publication Huixi Zhang
Laboratory of Molecular and Statistical Genetics, College of Life Sciences, Hunan Normal University, Changsha, Hunan 410081, China
1 shared publication
Latest Publications
- Open Access
A systematic dissection of human primary osteoblasts in vivo at single-cell resolution
Osteoblasts are multifunctional bone cells, which play essential roles in bone formation, angiogenesis regulation, as well as maintenance of hematopoiesis. Although both in vivo and in vitro studies on mice have identified several potential osteoblast subtypes based on their different transition stages or biological responses to external stimuli, the categorization of primary osteoblast subtypes in vivo in humans has not yet been achieved. Here, we used single-cell RNA sequencing (scRNA-seq) to perform a systematic cellular taxonomy dissection of freshly isolated human osteoblasts. Based on the gene expression patterns and cell lineage reconstruction, we identified three distinct cell clusters including preosteoblasts, mature osteoblasts, and an undetermined rare osteoblast subpopulation. This novel subtype was mainly characterized by the nuclear receptor subfamily 4 group A member 1 and 2 (NR4A1 and NR4A2), and its existence was confirmed by immunofluorescence staining. Trajectory inference analysis suggested that the undetermined cluster, together with the preosteoblasts, are involved in the regulation of osteoblastogenesis and also give rise to mature osteoblasts. Investigation of the biological processes and signaling pathways enriched in each subpopulation revealed that in addition to bone formation, preosteoblasts and undetermined osteoblasts may also regulate both angiogenesis and hemopoiesis. Finally, we demonstrated that there are systematic differences between the transcriptional profiles of human osteoblasts in vivo and mouse osteoblasts both in vivo and in vitro , highlighting the necessity for studying bone physiological processes in humans rather than solely relying on mouse models. Our findings provide novel insights into the cellular heterogeneity and potential biological functions of human primary osteoblasts at the single-cell level, which is an important and necessary step to further dissect the biological roles of osteoblasts in bone metabolism under various (patho-) physiological conditions.
Open AccessA systematic dissection of human primary osteoblasts in vivo at single-cell resolution
Osteoblasts are multifunctional bone cells, which play essential roles in bone formation, angiogenesis regulation, as well as maintenance of hematopoiesis. Although both in vivo and in vitro studies on mice have identified several potential osteoblast subtypes based on their different transition stages or biological responses to external stimuli, the categorization of primary osteoblast subtypes in vivo in humans has not yet been achieved. Here, we used single-cell RNA sequencing (scRNA-seq) to perform a systematic cellular taxonomy dissection of freshly isolated human osteoblasts. Based on the gene expression patterns and cell lineage reconstruction, we identified three distinct cell clusters including preosteoblasts, mature osteoblasts, and an undetermined rare osteoblast subpopulation. This novel subtype was mainly characterized by the nuclear receptor subfamily 4 group A member 1 and 2 (NR4A1 and NR4A2), and its existence was confirmed by immunofluorescence staining. Trajectory inference analysis suggested that the undetermined cluster, together with the preosteoblasts, are involved in the regulation of osteoblastogenesis and also give rise to mature osteoblasts. Investigation of the biological processes and signaling pathways enriched in each subpopulation revealed that in addition to bone formation, preosteoblasts and undetermined osteoblasts may also regulate both angiogenesis and hemopoiesis. Finally, we demonstrated that there are systematic differences between the transcriptional profiles of human osteoblasts in vivo and mouse osteoblasts both in vivo and in vitro , highlighting the necessity for studying bone physiological processes in humans rather than solely relying on mouse models. Our findings provide novel insights into the cellular heterogeneity and potential biological functions of human primary osteoblasts at the single-cell level, which is an important and necessary step to further dissect the biological roles of osteoblasts in bone metabolism under various (patho-) physiological conditions.
- 4 February 2020
- Published by Springer Nature
- p. 1015-1021
Platform of Examination Information Resources in Colleges and Universities Based on Big Data Deep Mining Technology
- 4 February 2020
- Published by Springer Nature
- p. 1015-1021
Platform of Examination Information Resources in Colleges and Universities Based on Big Data Deep Mining Technology
- 4 February 2020
- Published by Springer Nature
- p. 291-296
Regional Cooperative Strategy of Social Public Service Under the Background of Cloud Computing and Big Data Environment
- 4 February 2020
- Published by Springer Nature
- p. 291-296
Regional Cooperative Strategy of Social Public Service Under the Background of Cloud Computing and Big Data Environment