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2015 ; 130
(4
): 487-99
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Physiological amyloid-beta clearance in the periphery and its therapeutic
potential for Alzheimer s disease
#MMPMID26363791
Xiang Y
; Bu XL
; Liu YH
; Zhu C
; Shen LL
; Jiao SS
; Zhu XY
; Giunta B
; Tan J
; Song WH
; Zhou HD
; Zhou XF
; Wang YJ
Acta Neuropathol
2015[Oct]; 130
(4
): 487-99
PMID26363791
show ga
Amyloid-beta (A?) plays a pivotal role in the pathogenesis of Alzheimer's disease
(AD). The physiological capacity of peripheral tissues and organs in clearing
brain-derived A? and its therapeutic potential for AD remains largely unknown.
Here, we measured blood A? levels in different locations of the circulation in
humans and mice, and used a parabiosis model to investigate the effect of
peripheral A? catabolism on AD pathogenesis. We found that blood A? levels in the
inferior/posterior vena cava were lower than that in the superior vena cava in
both humans and mice. In addition, injected (125)I labeled A?40 was located
mostly in the liver, kidney, gastrointestinal tract, and skin but very little in
the brain; suggesting that A? derived from the brain can be cleared in the
periphery. Parabiosis before and after A? deposition in the brain significantly
reduced brain A? burden without alterations in the expression of amyloid
precursor protein, A? generating and degrading enzymes, A? transport receptors,
and AD-type pathologies including hyperphosphorylated tau, neuroinflammation, as
well as neuronal degeneration and loss in the brains of parabiotic AD mice. Our
study revealed that the peripheral system is potent in clearing brain A? and
preventing AD pathogenesis. The present work suggests that peripheral A?
clearance is a valid therapeutic approach for AD, and implies that deficits in
the A? clearance in the periphery might also contribute to AD pathogenesis.