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Vol. 15, Issue 8, 3863-3875, August 2004
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* Institute of Anatomy and Cell Biology, Göteborg University, SE-405 30 Gothenburg, Sweden;
Jagiellonian University, Faculty of Biotechnology, Biocenter, 30-387 Krakow, Poland; and
|| Department of Molecular Pathology, Graduate School of Medicine, University of Tokyo, Tokyo, Japan
Submitted August 12, 2003;
Revised May 31, 2004;
Accepted June 2, 2004
Monitoring Editor: Carl-Henrik Heldin
Bone morphogenetic proteins (BMPs) act as growth regulators and inducers of differentiation. They transduce their signal via three different type I receptors, termed activin receptor-like kinase 2 (Alk2), Alk3, or bone morphogenetic protein receptor Ia (BMPRIa) and Alk6 or BMPRIb. Little is known about functional differences between the three type I receptors. Here, we have investigated consequences of constitutively active (ca) and dominant negative (dn) type I receptor overexpression in adult-derived hippocampal progenitor cells (AHPs). The dn receptors have a nonfunctional intracellular but functional extracellular domain. They thus trap BMPs that are endogenously produced by AHPs. We found that effects obtained by overexpression of dnAlk2 and dnAlk6 were similar, suggesting similar ligand binding patterns for these receptors. Thus, cell survival was decreased, glial fibrillary acidic protein (GFAP) expression was reduced, whereas the number of oligodendrocytes increased. No effect on neuronal differentiation was seen. Whereas the expression of Alk2 and Alk3 mRNA remained unchanged, the Alk6 mRNA was induced after impaired BMP signaling. After dnAlk3 overexpression, cell survival and astroglial differentiation increased in parallel to augmented Alk6 receptor signaling. We conclude that endogenous BMPs mediate cell survival, astroglial differentiation and the suppression of oligodendrocytic cell fate mainly via the Alk6 receptor in AHP culture.
These authors were equally contributing second authors.
Corresponding author. E-mail address: anke.brederlau{at}anatcell.gu.se.
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