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Updated: Jul 7, 2026

Immunohistochemical Visualization of Hippocampal Neuron Activity After Spatial Learning in a Mouse Model of Neurodevelopmental Disorders
Published on: May 12, 2015
Exploring huntington's disease from a neurodevelopmental perspective
Chunhui Huang1, Xiao Zheng1, Wei Li1
1The Sixth Affiliated Hospital of Jinan University, Dongguan, 523710, China; State Key Laboratory of Bioactive Molecules and Druggability Assessment, Guangdong Basic Research Center of Excellence for Natural Bioactive Molecules and Discovery of Innovative Drugs, Guangdong Provincial Key Laboratory of Non-human Primate Research, Guangdong-Hong Kong-Macau Institute of CNS Regeneration, Jinan University, Guangzhou, 510632, China; Stomatological Hospital, School of Stomatology, Southern Medical University, Guangzhou, 510280, China.
Huntington's disease (HD) may stem from developmental issues, not just neuron death. Targeting mutant huntingtin (HTT) during neurodevelopment offers new therapeutic avenues for this inherited neurodegenerative disorder.
Area of Science:
- Neuroscience
- Genetics
- Developmental Biology
Background:
- Huntington's disease (HD) is an inherited neurodegenerative disorder caused by mutations in the huntingtin (HTT) gene.
- The traditional view of HD focuses on mutant huntingtin (mHTT) causing neuron death in the striatum.
- Emerging evidence suggests mHTT's impact on neurodevelopment offers an alternative perspective on HD pathogenesis.
Purpose of the Study:
- To review the role of HTT in neurodevelopment.
- To summarize the effects of mHTT on neurodevelopment across various models.
- To propose novel therapeutic strategies targeting early developmental interventions in HD.
Main Methods:
- Literature review synthesizing current knowledge on HD development and pathogenesis.
- Analysis of findings from diverse models investigating mHTT's impact on neurodevelopment.
- Exploration of connections between neurodevelopmental abnormalities and neurodegenerative processes in HD.
Main Results:
- The huntingtin protein (HTT) is crucial for normal neurodevelopment.
- Mutant HTT (mHTT) significantly disrupts neurodevelopmental processes.
- Different models reveal varied effects of mHTT on developing neural systems.
Conclusions:
- Rethinking HD as a neurodevelopmental disorder opens new therapeutic possibilities.
- Early intervention during development may alter HD progression.
- Understanding neurodevelopmental deficits is key to addressing HD pathogenesis.
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