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Published on: July 25, 2017
Mechanisms for removal of developmentally abnormal cells: cell competition and morphogenetic apoptosis
Takashi Adachi-Yamada1, Michael B O'Connor
1Department of Earth and Planetary System Sciences, Graduate School of Science and Technology, Kobe University, Kobe 657-8501. yamadach@kobe-u.ac.jp
Abstract:
Various cell differentiation signals are tightly linked with apoptotic signals. For example, as a result of somatic mutations, cells within a developing field occasionally receive an altered level of morphogenetic signaling that gives rise to an abnormal cell type. However, these developmentally abnormal cells are frequently removed by activating apoptotic signals. Although such phenomena are crucial for assuring normal development and maintaining a healthy state of various organs, the molecular mechanisms that sense aberrant signals and activate the apoptotic pathway(s) have not fully been investigated. In this review, we discuss recent progress in this area. Cell competition and morphogenetic apoptosis are two kinds of cell death, both of which are mediated by abnormal signaling of Dpp, a member of the TGF-beta superfamily that functions in Drosophila as a morphogen, mitogen and survival factor. Cell competition results in autonomous apoptosis induced by reduced reception of the extracellular survival factor Dpp, while morphogenetic apoptosis is nonautonomous, and is induced by contact of cells receiving different levels of Dpp signaling.
Insights
Cell differentiation and apoptosis are linked. Aberrant morphogenetic signaling triggers cell death, ensuring normal development. This review explores molecular mechanisms sensing abnormal signals and activating apoptosis, focusing on Dpp signaling in Drosophila.
Area of Science:
- Developmental Biology
- Cell Death Mechanisms
- Signal Transduction
Background:
- Cell differentiation and apoptosis are interconnected processes crucial for development and homeostasis.
- Aberrant morphogenetic signaling can lead to abnormal cell types, necessitating removal via apoptosis.
- Molecular mechanisms sensing aberrant signals and initiating apoptosis remain incompletely understood.
Purpose of the Study:
- To review recent advancements in understanding how aberrant signals trigger apoptosis during development.
- To discuss the roles of cell competition and morphogenetic apoptosis in development.
- To highlight the involvement of Decapentaplegic (Dpp) signaling in these processes.
Main Methods:
- Review of existing literature on cell competition, morphogenetic apoptosis, and Dpp signaling.
- Analysis of molecular mechanisms linking signal sensing to apoptotic pathways.
- Focus on studies utilizing Drosophila melanogaster as a model system.
Main Results:
- Cell competition involves autonomous apoptosis due to reduced Dpp signaling reception.
- Morphogenetic apoptosis is nonautonomous, induced by differential Dpp signaling levels between adjacent cells.
- Dpp, a transforming growth factor-beta superfamily member, acts as a morphogen, mitogen, and survival factor in Drosophila.
Conclusions:
- Understanding the interplay between differentiation and apoptotic signals is vital for developmental biology.
- Dpp signaling plays a critical role in mediating both cell competition and morphogenetic apoptosis.
- Further investigation into these molecular mechanisms can provide insights into maintaining tissue health and preventing developmental abnormalities.
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