Related Experiment Video
Updated: May 27, 2026

07:39
Mouse In Vivo Placental Targeted CRISPR Manipulation
Published on: April 14, 2023
Dystroglycan expression in human placenta: basement membrane localization and subunit distribution change between the
Reagan M Street1, Sara J Mucowski, Rheann Urrabaz-Garza
1Department of Obstetrics and Gynecology, University of Texas Medical Branch, Galveston, TX 77555, USA. rmstreet@utmb.edu
Reproductive Sciences (Thousand Oaks, Calif.)
|December 6, 2011
Summary
Dystroglycan (DG) is highly expressed in human trophoblasts, with its subunit localization varying by gestational age. This suggests DG may inhibit placental invasion, similar to its role in other cancers.
Area of Science:
- Reproductive biology
- Cellular and molecular biology
- Biochemistry
Background:
- Dystroglycan (DG) is a key component of the dystrophin-glycoprotein complex.
- Its role in placental development and function is not fully understood.
- Aberrant DG expression is implicated in various disease states.
Purpose of the Study:
- To investigate the distribution and expression patterns of dystroglycan (DG) subunits (α-DG and β-DG) in human placenta, membranes, and decidua.
- To correlate DG expression with trophoblast differentiation and gestational age.
Main Methods:
- Western blotting was used to assess DG protein levels.
- Immunohistochemistry and immunofluorescence microscopy were employed to determine the cellular and subcellular localization of α-DG and β-DG.
- Human placental tissues, fetal membranes, decidua, and cultured cells (including choriocarcinoma and HTR cells) were analyzed.
Main Results:
- Both α-DG and β-DG were detected in the syncytiotrophoblast of term placenta, with α-DG localized to the basement membrane.
- In first-trimester chorionic villi, α-DG and β-DG were found at the periphery of the cytotrophoblast.
- DG expression patterns varied in term fetal membranes; α-DG was undetectable in choriocarcinoma and HTR cells, while β-DG was present.
Conclusions:
- Dystroglycan is expressed at high levels in human trophoblasts.
- The localization of α-DG and β-DG subunits changes with gestational age and trophoblast differentiation.
- The observed expression pattern suggests a potential role for DG in inhibiting placental invasion, analogous to its function in cancer.
Related Concept Videos
Transcytosis of IgG
Transcytosis is the process in which molecules are internalized by endocytosis, transported across the cell, and released through exocytosis from the opposite end of the cell. Molecules such as insulin, immunoglobulins, and certain nutrients are transferred through the recycling endosomes by recycling and transcytosis.
IgG molecules from a mother undergo transcytosis starting around 13 weeks of gestation. The amount of IgG transferred and entering the fetal blood circulation increases with...
IgG molecules from a mother undergo transcytosis starting around 13 weeks of gestation. The amount of IgG transferred and entering the fetal blood circulation increases with...
Embryonic Connective Tissues
During early development, the embryo forms two types of connective tissues— the mesenchyme and mucoid connective tissue.
The mesenchyme is the first connective tissue that emerges in the developing embryo. It consists of loosely arranged multipotent mesenchymal cells and reticular fibers in the extracellular matrix. This loose arrangement allows easy migration of cells, which is essential for germ layer positioning, patterning, and organ morphogenesis during embryonic development. Mesenchyme is...
The mesenchyme is the first connective tissue that emerges in the developing embryo. It consists of loosely arranged multipotent mesenchymal cells and reticular fibers in the extracellular matrix. This loose arrangement allows easy migration of cells, which is essential for germ layer positioning, patterning, and organ morphogenesis during embryonic development. Mesenchyme is...
Cleavage and Blastulation
After a large-single-celled zygote is produced via fertilization, the process of cleavage occurs while zygotes travel through the uterine tube. Cleavage is a mitotic cell division that does not result in growth. With each round of successive cell division, daughter cells get increasingly smaller.
