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Updated: May 17, 2026

Analysis of Retinoic Acid-induced Neural Differentiation of Mouse Embryonic Stem Cells in Two and Three-dimensional Embryoid Bodies
Published on: April 22, 2017
Activin and TGF-β effects on brain development and neural stem cells
Griselda Rodríguez-Martínez1, Iván Velasco
1Instituto de Fisiologia Celular- Neurociencias, Universidad Nacional Autonoma de Mexico, Mexico D.F., Mexico.
Abstract:
Transforming Growth Factor-β (TGF-β) family members are ubiquitously expressed, participating in the regulation of many processes in different cell types both in embryonic and adult stages. Several members of this family, including Activins, TGF-β1-3 and Nodal, have been implicated in the development and maintenance of various organs, in which stem cells play important roles. Although TGF-β was initially considered an injury-related cytokine, it became clear that not only TGF-β, but other members of this family, play critical roles in morphogenesis and cell lineage specification. During brain development, Activin and TGF-βs as well as their cognate receptors, are expressed in different patterns. The roles of Activin and TGF-β during CNS development are sometimes contradictory, because these proteins present different actions depending on the cell type and the context. The aim of this review is to summarize current information on the actions of TGF-β members during developing brain, and also on Neural Stem/Progenitor Cells (NSPC). We focus on the TGF-β subgroup, specifically on the effects of TGF-β1 and Activin A. In the first section we describe the main characteristics of the ligands, its receptors as well as the proteins and mechanisms involved in signaling. Next, we discuss the main advances concerning TGF-β1 and Activin actions during brain development and their roles in NSPC fate decision and neuroprotection both in vitro and in vivo. The emerging picture from these studies suggests that these growth factors can be used to manipulate neurogenesis and might help to achieve restoration after brain deterioration.
Insights
Transforming Growth Factor-β (TGF-β) and Activin A are key regulators in brain development and neural stem cell function. These growth factors influence neurogenesis and hold potential for brain repair after injury.
Area of Science:
- Neuroscience
- Developmental Biology
- Cell Biology
Background:
- Transforming Growth Factor-β (TGF-β) family members regulate crucial cellular processes during embryonic and adult development.
- Activins and TGF-βs are implicated in organ development and stem cell maintenance, including roles in brain morphogenesis.
- Initially viewed as injury-related, TGF-β family members are now recognized for critical roles in cell lineage specification and development.
Purpose of the Study:
- To review the actions of TGF-β family members during brain development.
- To summarize the roles of TGF-β1 and Activin A in Neural Stem/Progenitor Cells (NSPC).
- To explore the potential of these growth factors in neuroprotection and brain repair.
Main Methods:
- Literature review of studies on TGF-β members, Activin A, and their signaling pathways.
- Analysis of expression patterns and functions during central nervous system (CNS) development.
- Examination of in vitro and in vivo data on NSPC fate and neuroprotection.
Main Results:
- TGF-β and Activin signaling pathways are complex, with context-dependent and sometimes contradictory effects on CNS development.
- TGF-β1 and Activin A play significant roles in regulating NSPC fate decisions, including proliferation and differentiation.
- These growth factors demonstrate neuroprotective effects and influence neurogenesis in various models.
Conclusions:
- TGF-β1 and Activin A are critical regulators of brain development and NSPC behavior.
- Their distinct actions highlight the complexity of TGF-β signaling in the developing brain.
- Targeting these growth factors offers potential therapeutic strategies for brain injury and neurodegenerative diseases.
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