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Fibroblast growth factor 8: Multifaceted role in development and developmental disorder
Huamin Yin1,2, Lian Duan2, Zhendong Wang3
1Institute of Life Sciences, College of Life and Environmental Sciences, Wenzhou University, Wenzhou, Zhejiang 325035, China.
Fibroblast growth factor 8 (FGF8) is vital for embryonic development, regulating cell functions and organogenesis. Aberrant FGF8 signaling causes severe developmental abnormalities, impacting multiple organ systems.
Area of Science:
- Developmental Biology
- Molecular Signaling
- Genetics
Background:
- Fibroblast growth factor 8 (FGF8) is a secreted signaling molecule essential for embryonic development.
- FGF8 regulates critical cellular processes including survival, proliferation, migration, and differentiation.
- Its dynamic expression pattern is crucial for the proper formation of various embryonic structures.
Purpose of the Study:
- To comprehensively review FGF8 expression patterns in humans and mice.
- To summarize FGF8's role in the development of craniofacial structures, limbs, cardiovascular and urogenital systems, nephrogenesis, lungs, and brain.
- To explore developmental abnormalities linked to dysregulated FGF8 signaling.
Main Methods:
- Literature review of studies on FGF8 expression and function.
- Analysis of FGF8's involvement in diverse embryonic tissues.
- Compilation of data on FGF8-related developmental disorders.
Main Results:
- FGF8 exhibits dynamic spatiotemporal expression during embryogenesis.
- FGF8 is indispensable for craniofacial, limb, organ, and brain development.
- Dysregulation of FGF8 leads to multiorgan abnormalities, including skeletal defects, ciliopathies, and holoprosencephaly.
Conclusions:
- FGF8 is a key regulator of embryonic organogenesis and tissue development.
- Precise control of FGF8 localization and dosage is critical for normal development.
- Aberrant FGF8 signaling underlies a spectrum of congenital abnormalities.
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