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Updated: May 25, 2026

A Murine Pancreatic Islet Cell-based Screening for Diabetogenic Environmental Chemicals
Published on: June 25, 2018
Bone marrow microenvironment: a newly recognized target for diabetes-induced cellular damage.
Giuseppe Mangialardi1, Atsuhiko Oikawa, Carlotta Reni
1Chair of Experimental Cardiovascular Medicine, Bristol Heart Institute, School of Clinical Sciences, University of Bristol, Bristol, UK.
Diabetes impairs bone marrow progenitor cells crucial for tissue repair, leading to worse cardiovascular outcomes. This review details diabetes-induced damage to these cells in their niches.
Area of Science:
- Cardiovascular Medicine
- Regenerative Medicine
- Hematology
Background:
- Diabetes mellitus is strongly linked to cardiovascular morbidity and mortality.
- Diabetic patients experience more frequent and severe cardiovascular events.
- Impaired cellular regeneration contributes to poorer tissue healing in diabetes.
Purpose of the Study:
- To review evidence on diabetes-induced damage to bone marrow progenitor cells.
- To explore the impact of diabetes on cell mobilization, recruitment, and function.
- To highlight damage within endosteal and vascular niches of bone marrow.
Main Methods:
- Literature review of current evidence.
- Analysis of studies on progenitor cell function in diabetes.
- Examination of bone marrow niches (endosteal and vascular).
Main Results:
- Diabetes negatively affects the mobilization and recruitment of bone marrow-derived progenitor cells.
- Intrinsic functional properties of these progenitor cells are impaired by diabetes.
- Evidence points to diabetes-induced damage in both endosteal and vascular bone marrow niches.
Conclusions:
- Diabetes compromises the regenerative capacity by damaging bone marrow progenitor cells.
- This damage contributes to the increased cardiovascular complications observed in diabetic patients.
- Understanding these mechanisms is vital for improving therapeutic strategies in diabetes.
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