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Updated: May 8, 2026

Expansion and Adipogenesis Induction of Adipocyte Progenitors from Perivascular Adipose Tissue Isolated by Magnetic Activated Cell Sorting
Published on: June 30, 2017
Osteoblast-adipocyte lineage plasticity in tissue development, maintenance and pathology
Agnes D Berendsen1, Bjorn R Olsen
1Department of Developmental Biology, REB 413, Harvard School of Dental Medicine, 188 Longwood Ave, Boston, MA, 02115, USA, Agnes_Berendsen@hsdm.harvard.edu.
Osteoblasts and adipocytes originate from a common precursor cell, with plasticity between these cell types impacting bone health and disease. Understanding their differentiation is key to identifying disease-related factors.
Area of Science:
- Bone biology
- Cell biology
- Stem cell research
Background:
- Osteoblasts (bone-forming cells) and adipocytes (fat cells) arise from a shared progenitor in bone marrow.
- Plasticity exists between osteoblast and adipocyte lineages, influencing bone homeostasis and disease.
- Imbalances in these cell populations are implicated in osteoporosis and other conditions.
Purpose of the Study:
- To review the complex microenvironment controlling osteoblast and adipocyte differentiation.
- To highlight the importance of understanding precursor cell plasticity for disease pathophysiology.
- To identify key regulatory mechanisms in osteogenesis and adipogenesis.
Main Methods:
- Literature review of transcriptional regulators.
- Analysis of signaling pathways and epigenetic mechanisms (DNA methylation, chromatin remodeling, microRNAs).
- Examination of precursor cell microenvironment in development, maintenance, and pathology.
Main Results:
- Transcriptional regulators play a critical role in controlling cell differentiation.
- Complex signaling crosstalk and epigenetic factors govern cell commitment.
- The precursor cell microenvironment is a crucial determinant of cell fate.
Conclusions:
- Understanding osteoblast and adipocyte differentiation and trans-differentiation is vital for disease research.
- Epigenetic mechanisms and signaling pathways are key regulators of cell lineage commitment.
- Targeting these pathways may offer therapeutic strategies for bone-related diseases.
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