Related Experiment Video
Updated: Dec 25, 2025

07:39
Mouse In Vivo Placental Targeted CRISPR Manipulation
Published on: April 14, 2023
3.4K
Placental Galectin-2 Expression in Gestational Diabetes: A Systematic, Histological Analysis
Paula Hepp1, Laura Unverdorben1,2, Stefan Hutter1
1Department of Gynecology and Obstetrics, University Hospital, LMU Munich, Maistraße 11, 80337 Munich, Germany.
International Journal of Molecular Sciences
|April 5, 2020
Summary
Gestational diabetes mellitus (GDM) involves chronic inflammation. This study found increased galectin-2 in GDM placentas, suggesting its role in pregnancy complications and potentially long-term offspring health.
Area of Science:
- Immunology
- Endocrinology
- Reproductive Biology
Background:
- Gestational diabetes mellitus (GDM) is a common pregnancy disorder linked to inflammation.
- The underlying molecular mechanisms of GDM, particularly immune system involvement, require further elucidation.
- Galectin-2 is known to modulate immune cell activity.
Purpose of the Study:
- To investigate galectin-2 expression in placentas from GDM patients and controls.
- To analyze expression in a sex-specific manner.
- To characterize the cell types expressing galectin-2 in GDM placentas.
Main Methods:
- Placental tissue samples from 40 GDM patients and 40 controls were analyzed.
- Immunohistochemistry was employed for semi-quantitative expression analysis.
- Double immunofluorescence was used to identify galectin-2 expressing cell phenotypes.
Main Results:
- Galectin-2 was significantly upregulated in the syncytiotrophoblast and decidua of GDM placentas.
- Strong galectin-2 expression was observed in extra-villous trophoblast cells and fetal endothelial cells in GDM.
- This represents the first systematic investigation of galectin-2 in GDM.
Conclusions:
- Galectin-2 is upregulated in the placenta during gestational diabetes mellitus.
- These findings contribute to understanding GDM's inflammatory pathways and galectin-2's role.
- The results may have implications for the long-term cardiovascular health of offspring affected by GDM.
Related Concept Videos
Pathophysiology of Diabetes
2.9K
Diabetes mellitus is a chronic metabolic disorder characterized by hyperglycemia. The four categories of diabetes are type 1 diabetes, type 2 diabetes, other specific types of diabetes, and gestational diabetes.
Type 1 diabetes is characterized by autoimmune-mediated destruction of pancreatic β cells, with environmental factors potentially triggering this process in genetically susceptible individuals. Despite many not having a family history, certain genes increase susceptibility,...
Type 1 diabetes is characterized by autoimmune-mediated destruction of pancreatic β cells, with environmental factors potentially triggering this process in genetically susceptible individuals. Despite many not having a family history, certain genes increase susceptibility,...
2.9K
Diabetes Mellitus: Type 2 and Gestational
4.2K
Type 2 diabetes, characterized by insulin resistance, arises when the insulin receptors on cells lose responsiveness to insulin, diminishing the cell's capacity to take up glucose, resulting in elevated blood glucose levels. To receive a diagnosis of Type 2 diabetes, a series of blood glucose tests are necessary to assess whether the blood glucose falls within normal parameters. If the result is out of the normal range, a patient may be diagnosed as prediabetic or diabetic, depending on the...
4.2K
Glucose Transporters
27.0K
Glucose transporters facilitate the transport of glucose across the cell membrane. In addition to glucose, some glucose transporters can also aid the movement of other hexoses such as fructose, mannose, and galactose.
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
Facilitated diffusion-glucose transporters (GLUTs) are encoded by the solute-linked carrier (SLC) family 2, subfamily A gene family, or SLC2A. The 14 GLUT protein members are distributed into three classes:
27.0K

