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Human Body & Health

Why does mutant huntingtin protein clearance via autophagy decline in Huntington's disease?

A)Microglia cease phagocytic activity
B)Lysosomal enzyme production halts entirely
C)mTOR activation inhibits autophagosome formation
D)Proteasome degradation rate sharply increases

💡 Explanation

mTOR activation suppresses autophagy by inhibiting the ULK1 complex, which is essential for autophagosome formation; because mTOR is hyperactive in Huntington's disease, it impairs mutant huntingtin clearance. Therefore, autophagy is less effective, rather than phagocytosis or proteasome activity being the primary issue.

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