Autosomal-dominant Alzheimer's disease mutations at the same codon of amyloid precursor protein differentially alter A beta production

作者：Suarez Calvet Marc; Belbin Olivia; Pera Marta; Badiola Nahuai; Magrane Jordi; Guardia Laguarta Cristina; Munoz Laila; Colom Cadena Marti; Clarimon Jordi; Lleo Alberto^*

来源：Journal of Neurochemistry, 2014, 128(2): 330-339.

DOI：10.1111/jnc.12466

• Alzheimer's disease
• amyloid-beta peptide
• APP mutations
• presenilin
• gamma-secretase

Autosomal-dominant Alzheimer's disease (ADAD) is a genetic disorder caused by mutations in Amyloid Precursor Protein (APP) or Presenilin (PSEN) genes. Studying the mechanisms underlying these mutations can provide insight into the pathways that lead to AD pathology. The majority of biochemical studies on APP mutations to-date have focused on comparing mechanisms between mutations at different codons. It has been assumed that amino acid position is a major determinant of protein dysfunction and clinical phenotype. However, the differential effect of mutations at the same codon has not been sufficiently addressed. In the present study we compared the effects of the aggressive ADAD-associated APP I716F mutation with I716V and I716T on APP processing in human neuroglioma and CHO-K1 cells. All APP I716 mutations increased the ratio of A beta 42/40 and changed the product line preference of gamma-secretase towards A beta 38 production. In addition, the APP I716F mutation impaired the epsilon-cleavage and the fourth cleavage of gamma-secretase and led to abnormal APP beta-CTF accumulation at the plasma membrane. Taken together, these data indicate that APP mutations at the same codon can induce diverse abnormalities in APP processing, some resembling PSEN1 mutations. These differential effects could explain the clinical differences observed among ADAD patients bearing different APP mutations at the same position.

• 出版日期2014-1