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Updated: May 25, 2026

Evaluation of Hepatic Glucose Production in a Polycystic Ovary Syndrome Mouse Model
Published on: March 5, 2022
Glucose-induced increase in circulating progenitor cells is blunted in polycystic amenorrhoeic subjects
Soumi Bairagi1, Jayashree Gopal, Abel A Nathan
1Laboratory of Vascular Biology, Department of Biotechnology, Indian Institute of Technology Madras, BT 415, Chennai 600036, India.
Insights
Glucose challenge increases bone marrow stem cells in healthy women, but this response is blunted in amenorrheic women. Endothelial progenitor cell function is also impaired in amenorrheic subjects.
Area of Science:
- Reproductive Endocrinology
- Stem Cell Biology
- Metabolic Health
Background:
- The glucose-induced kinetics of bone marrow-derived stem cells in healthy females is not well understood.
- Previous research has not fully elucidated the impact of amenorrhea on these stem cell responses.
- Endothelial progenitor cell (EPC) differentiation potential in amenorrheic women requires further investigation.
Purpose of the Study:
- To determine if circulating CD133(+), CD34(+), and CD133(+)CD34(+) cells increase following a glucose load in healthy females.
- To investigate whether this stem cell response is altered in women with amenorrhea.
- To compare the endothelial differentiation capacity of peripheral blood-derived EPCs between healthy and amenorrheic women.
Main Methods:
- A case-control study involving 44 amenorrheic subjects and 36 healthy females.
- Measurement of circulating bone marrow-derived stem cells using two-color direct flow cytometry.
- Characterization of cultured progenitor cells for endothelial markers and nitric oxide (NO) production.
Main Results:
- Amenorrheic subjects exhibited insulin resistance and reduced fasting levels of CD133(+), CD34(+), and CD133(+)CD34(+) cells.
- Controls showed a 1.5 to 2-fold increase in these cells post-glucose load, a response significantly blunted in amenorrheic subjects.
- Cultured cells from amenorrheic subjects displayed reduced adherence and lower endothelial nitric-oxide synthase and NO production.
Conclusions:
- The oral glucose-induced increase in circulating CD133(+) and CD133(+)CD34(+) cells is attenuated in insulin-resistant amenorrheic subjects.
- Endothelial differentiation potential of peripheral blood-derived EPCs is also diminished in this population.
- These findings highlight altered stem cell kinetics and function in amenorrheic women, potentially linked to insulin resistance.
Background:
Glucose-induced kinetics of bone marrow-derived stem cells in healthy females is presently unknown. The objectives of this study were to determine whether circulating levels of CD133(+), CD34(+) and CD133(+)CD34(+) cells increase in response to glucose load in healthy females and whether the kinetics is altered in amenorrhoeic women. The other objective of the work was to compare the endothelial differentiation potential of peripheral blood-derived endothelial progenitor cells (EPCs) from healthy versus amenorrhoeic women.
Methods:
In this case-control study, 44 amenorrhoeic subjects and 36 age-matched females with no menstrual disturbance were recruited at Apollo Hospitals, a Tertiary health care center in Chennai, India. Circulating bone marrow-derived stem cells were measured by two color direct flow cytometry. Cultured progenitor cells were characterized at Day 7 and 14 for expression of endothelial markers and production of nitric oxide (NO) via immunofluoroscence.
Results:
The amenorrhoeic subjects were insulin resistant with homeostatic model of assessment of insulin resistance values of 3.33 ± 0.3 versus 1.75 ± 0.148 observed for controls (P< 0.0001). Among the amenorrhoeic subjects, 38 subjects had polycystic ovaries with no signs of hyperandrogenism. Fasting levels of CD133(+), CD34(+) and CD133(+)CD34(+) cells were reduced in amenorrhoeic subjects (P< 0.001). There was a 1.5 to 2-fold increase in the circulating levels of these cells in response to 75 g oral glucose challenge at 1 and 2 h post-load conditions in controls, which was significantly blunted for CD133(+) (P< 0.001) and CD133(+)CD34(+) (P< 0.001) cells in amenorrhoeic subjects. A positive correlation was observed between estrogen and fasting CD133(+) (r= 0.205, P= 0.070), CD34(+) (r= 0.249, P= 0.027) and CD133(+)CD34(+) (r= 0.217, P= 0.055) cell counts. Additionally, fasting counts for CD34(+) and CD133(+)CD34(+) cells positively correlated with FSH and inversely correlated with LH and C-peptide in the polycystic group. Cultured cells from polycystic subjects exhibited reduced adherence to fibronectin and expressed lower levels of endothelial nitric-oxide synthase and NO.
Conclusions:
Oral glucose-induced increase in circulating numbers of CD133(+) and CD133(+)CD34(+) cells and endothelial differentiation potential of peripheral blood-derived EPCs is attenuated in insulin resistant amenorrhoeic subjects.
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