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Updated: May 27, 2026

Enumeration of Neural Stem Cells Using Clonal Assays
Published on: October 4, 2016
JAM-C is an apical surface marker for neural stem cells
Sandra Stelzer1, Maik M A Worlitzer, Lamia'a Bahnassawy
1Institute of Cell Biology, Stem Cell Biology and Regeneration Group, Westfälische Wilhelms-Universität Münster, ZMBE, Münster, Germany.
Insights
Junctional adhesion molecule-C (JAM-C) is expressed in neural stem cells (NSCs) and progenitor cells. This protein is asymmetrically distributed during cell division, identifying it as a novel marker for neural stem cells.
Area of Science:
- Neuroscience
- Cell Biology
- Developmental Biology
Background:
- Junctional adhesion molecule-C (JAM-C) is a cell surface protein involved in cell-cell adhesion.
- Neural stem cells (NSCs) are highly polarized and their self-renewal relies on controlled cell divisions.
- The distribution of apical membrane components influences NSC division asymmetry.
Purpose of the Study:
- To investigate the expression and localization of JAM-C in neural stem cells.
- To determine if JAM-C plays a role in the asymmetric cell divisions of NSCs.
Main Methods:
- Immunohistochemistry on embryonic and adult mouse brain tissue.
- Analysis of JAM-C expression and localization in neural progenitor and stem cells.
- In vivo studies to observe JAM-C distribution during cell division.
Main Results:
- JAM-C is expressed in neural progenitor cells and neural stem cells in both embryonic and adult mouse brains.
- JAM-C is enriched at the apical surface of these cells.
- JAM-C exhibits asymmetric distribution during neural stem cell division.
Conclusions:
- JAM-C is identified as a novel surface marker for neural stem cells.
- The asymmetric distribution of JAM-C suggests a role in regulating NSC division.
- JAM-C may be important for maintaining neural stem cell populations.
Abstract:
Junctional adhesion molecule-C (JAM-C) is an adhesive cell surface protein expressed in various cell types. JAM-C localizes to the apically localized tight junctions (TJs) between contacting endothelial and epithelial cells, where it contributes to cell-cell adhesions. Just as those epithelial cells, also neural stem cells are highly polarized along their apical-basal axis. The defining feature of all stem cells, including neural stem cells (NSCs) is their ability to self renew. This self-renewal depends on the tight control of symmetric and asymmetric cell divisions. In NSCs, the decision whether a division is symmetric or asymmetric largely depends on the distribution of the apical membrane and cell fate determinants on the basal pole of the cell. In this study we demonstrate that JAM-C is expressed on neural progenitor cells and neural stem cells in the embryonic as well as the adult mouse brain. Furthermore, we demonstrate that in vivo JAM-C shows enrichment at the apical surface and therefore is asymmetrically distributed during cell divisions. These results define JAM-C as a novel surface marker for neural stem cells.
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