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Loss of kallikrein-related peptidase 7 exacerbates amyloid pathology in Alzheimer's disease model mice.

Kiwami Kidana | Takuya Tatebe | Kaori Ito | Norikazu Hara | Akiyoshi Kakita | Takashi Saito | Sho Takatori | Yasuyoshi Ouchi | Takeshi Ikeuchi | Mitsuhiro Makino | Takaomi C Saido | Masahiro Akishita | Takeshi Iwatsubo | Yukiko Hori | Taisuke Tomita
EMBO molecular medicine | 2018

Deposition of amyloid-β (Aβ) as senile plaques is one of the pathological hallmarks in the brains of Alzheimer's disease (AD) patients. In addition, glial activation has been found in AD brains, although the precise pathological role of astrocytes remains unclear. Here, we identified kallikrein-related peptidase 7 (KLK7) as an astrocyte-derived Aβ degrading enzyme. Expression of KLK7 mRNA was significantly decreased in the brains of AD patients. Ablation of Klk7 exacerbated the thioflavin S-positive Aβ pathology in AD model mice. The expression of Klk7 was upregulated by Aβ treatment in the primary astrocyte, suggesting that Klk7 is homeostatically modulated by Aβ-induced responses. Finally, we found that the Food and Drug Administration-approved anti-dementia drug memantine can increase the expression of Klk7 and Aβ degradation activity specifically in the astrocytes. These data suggest that KLK7 is an important enzyme in the degradation and clearance of deposited Aβ species by astrocytes involved in the pathogenesis of AD.

Pubmed ID: 29311134

Associated grants

  • Agency: NIA NIH HHS, United States
    Id: P50 AG016574
  • Agency: NIH HHS, United States
    Id: UM1 OD023221
  • Agency: NIA NIH HHS, United States
    Id: R01 AG032990
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS080820
  • Agency: NIA NIH HHS, United States
    Id: U01 AG046139
  • Agency: NIA NIH HHS, United States
    Id: P01 AG003949
  • Agency: NINDS NIH HHS, United States
    Id: U24 NS072026
  • Agency: NIA NIH HHS, United States
    Id: P30 AG019610
  • Agency: NIA NIH HHS, United States
    Id: P50 AG025711
  • Agency: NIA NIH HHS, United States
    Id: P01 AG017216
  • Agency: NIA NIH HHS, United States
    Id: R01 AG018023
  • Agency: NIA NIH HHS, United States
    Id: U01 AG006786

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