Lack of huntingtin-associated protein-1 causes neuronal death resembling hypothalamic degeneration in Huntington's disease

SH Li, ZX Yu, CL Li, HP Nguyen, YX Zhou… - Journal of …, 2003 - Soc Neuroscience
SH Li, ZX Yu, CL Li, HP Nguyen, YX Zhou, C Deng, XJ Li
Journal of Neuroscience, 2003Soc Neuroscience
Huntington's disease (HD) is caused by a polyglutamine expansion in the disease protein
huntingtin. The polyglutamine expansion causes huntingtin to interact abnormally with a
number of proteins. However, it is unclear whether, and how, huntingtin-associated proteins
are involved in the neurodegeneration in HD. Here, we show that huntingtin-associated
protein-1 (HAP1), which is involved in intracellular trafficking of epidermal growth factor
receptor (EGFR), is highly expressed in the hypothalamus. Mice lacking HAP1 die after birth …
Huntington's disease (HD) is caused by a polyglutamine expansion in the disease protein huntingtin. The polyglutamine expansion causes huntingtin to interact abnormally with a number of proteins. However, it is unclear whether, and how, huntingtin-associated proteins are involved in the neurodegeneration in HD. Here, we show that huntingtin-associated protein-1 (HAP1), which is involved in intracellular trafficking of epidermal growth factor receptor (EGFR), is highly expressed in the hypothalamus. Mice lacking HAP1 die after birth because of depressed feeding activity. Terminal deoxynucleotidyl transferase-mediated biotinylated UTP nick end labeling staining and electron microscopic examination revealed the degeneration in hypothalamic regions that control feeding behavior. Hypothalamic degeneration was also observed in HD transgenic mice that have a significant loss of body weight. Inhibition of HAP1 expression decreases EGFR signaling and cell viability, whereas overexpression of HAP1 enhances this signaling activity and inhibits mutant huntingtin-mediated cytotoxicity. These results suggest that the effect of mutant huntingtin on HAP1 and EGFR signaling may contribute to the hypothalamic neurodegeneration and loss of body weight in HD.
Soc Neuroscience