Production of the Alzheimer Amyloid β Protein by Normal Proteolytic Processing

Mikio Shoji(Gunma University), Todd E. Golde(Case Western Reserve University), Jorge Ghiso(Columbia University Irving Medical Center), Tobun T. Cheung(Case Western Reserve University), Steven Estus(Washington University in St. Louis), Lillian M. Shaffer(Case Western Reserve University), Xiao-Dan Cai(Case Western Reserve University), Deborah M. McKay(Case Western Reserve University), Ron Tintner(The University of Texas Southwestern Medical Center), B Frangione(Columbia University Irving Medical Center), Steven G. Younkin(Case Western Reserve University)
Science
October 2, 1992
Cited by 1,445

Abstract

The 4-kilodalton (39 to 43 amino acids) amyloid beta protein (beta AP), which is deposited as amyloid in the brains of patients with Alzheimer's diseases, is derived from a large protein, the amyloid beta protein precursor (beta APP). Human mononuclear leukemic (K562) cells expressing a beta AP-bearing, carboxyl-terminal beta APP derivative released significant amounts of a soluble 4-kilodalton beta APP derivative essentially identical to the beta AP deposited in Alzheimer's disease. Human neuroblastoma (M17) cells transfected with constructs expressing full-length beta APP and M17 cells expressing only endogenous beta APP also released soluble 4-kilodalton beta AP, and a similar, if not identical, fragment was readily detected in cerebrospinal fluid from individuals with Alzheimer's disease and normal individuals. Thus cells normally produce and release soluble 4-kilodalton beta AP that is essentially identical to the 4-kilodalton beta AP deposited as insoluble amyloid fibrils in Alzheimer's disease.


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