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Isolation, Culture, and Differentiation of Bone Marrow Stromal Cells and Osteoclast Progenitors from Mice
Published on: January 6, 2018
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Effect of aged bone marrow microenvironment on mesenchymal stem cell migration.
Yan-Mei Yang1, Ping Li, Dian-Chao Cui
1Chinese PLA General Hospital, 28 Fuxing Road, Haidian District, Beijing, 100850, People's Republic of China.
Age (Dordrecht, Netherlands)
|February 20, 2015
Summary
Bone marrow from aged mice impairs mesenchymal stem cell (MSC) migration, not proliferation. This age-related decrease in MSC migration is linked to reduced JNK pathway activation.
Area of Science:
- Stem cell biology
- Aging research
- Immunology
Background:
- Mesenchymal stem cells (MSCs) possess multipotent differentiation and immunoregulatory capabilities.
- The bone marrow (BM) microenvironment influences MSC properties, but its age-related effects remain unclear.
Purpose of the Study:
- To investigate how the aged BM microenvironment affects MSC characteristics, specifically colony formation, proliferation, and migration.
Main Methods:
- Comparative analysis of BM from young and aged mice.
- Flow cytometry to assess immune cell populations.
- Co-culture experiments with murine MSC cell line C3H10T1/2.
- Assessment of MSC proliferation and migration.
- Western blot analysis for JNK pathway phosphorylation.
Main Results:
- Aged BM reduced MSC colony formation.
- Aged BM did not affect MSC proliferation but significantly decreased MSC migration.
- Reduced JNK pathway phosphorylation was observed in MSCs co-cultured with aged BM.
Conclusions:
- The aged BM microenvironment impairs MSC migration, not proliferation.
- Age-related changes in the BM niche affect MSC homing and function.
- The JNK signaling pathway is implicated in the reduced migration of MSCs in aged individuals.
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