Literature DB >> 11522960

Expression of the kallikrein gene family in normal and Alzheimer's disease brain.

C Shimizu-Okabe1, G M Yousef, E P Diamandis, S Yoshida, S Shiosaka, M Fahnestock.   

Abstract

The human kallikrein gene family consists of 15 serine proteases. We examined the expression of the kallikrein genes in human cerebral cortex and hippocampus by RT-PCR and compared their expression between Alzheimer's disease (AD) and control tissue. KLK1, 4, 5, 6, 7, 8, 10, 11, 13 and 14 are expressed in both cerebral cortex and hippocampus. KLK9 is expressed in cortex but not hippocampus, whereas KLK2, 3, 12 and 15 are not expressed in either tissue. We demonstrate an 11.5-fold increase in KLK8 mRNA levels in AD hippocampus compared to controls. The KLK8 gene product, neuropsin, processes extracellular matrix and is important for neuronal plasticity. Therefore, the increase in KLK8 could have detrimental effects on hippocampal function in AD.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11522960     DOI: 10.1097/00001756-200108280-00031

Source DB:  PubMed          Journal:  Neuroreport        ISSN: 0959-4965            Impact factor:   1.837


  14 in total

1.  Differential expression of multiple kallikreins in a viral model of multiple sclerosis points to unique roles in the innate and adaptive immune response.

Authors:  Michael Panos; George P Christophi; Moses Rodriguez; Isobel A Scarisbrick
Journal:  Biol Chem       Date:  2014-09       Impact factor: 3.915

2.  Kallikrein cascades in traumatic spinal cord injury: in vitro evidence for roles in axonopathy and neuron degeneration.

Authors:  Maja Radulovic; Hyesook Yoon; Nadya Larson; Jianmin Wu; Rachel Linbo; Joshua E Burda; Eleftherios P Diamandis; Sachiko I Blaber; Michael Blaber; Michael G Fehlings; Isobel A Scarisbrick
Journal:  J Neuropathol Exp Neurol       Date:  2013-11       Impact factor: 3.685

3.  A cardinal sin when researching neuropsin/KLK8: Thou shalt validate antibodies.

Authors:  Debomoy K Lahiri; Arpita Konar; Mahendra K Thakur; Bryan Maloney
Journal:  Alzheimers Dement       Date:  2017-07-18       Impact factor: 21.566

4.  Targeted disruption of SPI3/Serpinb6 does not result in developmental or growth defects, leukocyte dysfunction, or susceptibility to stroke.

Authors:  Katrina L Scarff; Kheng S Ung; Harshal Nandurkar; Peter J Crack; Catherina H Bird; Phillip I Bird
Journal:  Mol Cell Biol       Date:  2004-05       Impact factor: 4.272

Review 5.  Heparin oligosaccharides as potential therapeutic agents in senile dementia.

Authors:  Qing Ma; Umberto Cornelli; Israel Hanin; Walter P Jeske; Robert J Linhardt; Jeanine M Walenga; Jawed Fareed; John M Lee
Journal:  Curr Pharm Des       Date:  2007       Impact factor: 3.116

6.  Clinical relevance of kallikrein-related peptidase 6 (KLK6) and 8 (KLK8) mRNA expression in advanced serous ovarian cancer.

Authors:  Nancy Ahmed; Julia Dorn; Rudolf Napieralski; Enken Drecoll; Matthias Kotzsch; Peter Goettig; Eman Zein; Stefanie Avril; Marion Kiechle; Eleftherios P Diamandis; Manfred Schmitt; Viktor Magdolen
Journal:  Biol Chem       Date:  2016-12-01       Impact factor: 3.915

Review 7.  Natural and synthetic inhibitors of kallikrein-related peptidases (KLKs).

Authors:  Peter Goettig; Viktor Magdolen; Hans Brandstetter
Journal:  Biochimie       Date:  2010-07-06       Impact factor: 4.079

8.  Kallikrein-related peptidases 6 and 10 are elevated in cerebrospinal fluid of patients with Alzheimer's disease and associated with CSF-TAU and FDG-PET.

Authors:  Oliver Goldhardt; Inanna Warnhoff; Igor Yakushev; Ilijana Begcevic; Hans Förstl; Viktor Magdolen; Antoninus Soosaipillai; Eleftherios Diamandis; Panagiotis Alexopoulos; Timo Grimmer
Journal:  Transl Neurodegener       Date:  2019-08-27       Impact factor: 8.014

9.  Early and sustained altered expression of aging-related genes in young 3xTg-AD mice.

Authors:  V Gatta; M D'Aurora; A Granzotto; L Stuppia; S L Sensi
Journal:  Cell Death Dis       Date:  2014-02-13       Impact factor: 8.469

10.  Integrated analysis of human genetic association study and mouse transcriptome suggests LBH and SHF genes as novel susceptible genes for amyloid-β accumulation in Alzheimer's disease.

Authors:  Yumi Yamaguchi-Kabata; Takashi Morihara; Tomoyuki Ohara; Toshiharu Ninomiya; Atsushi Takahashi; Hiroyasu Akatsu; Yoshio Hashizume; Noriyuki Hayashi; Daichi Shigemizu; Keith A Boroevich; Manabu Ikeda; Michiaki Kubo; Masatoshi Takeda; Tatsuhiko Tsunoda
Journal:  Hum Genet       Date:  2018-07-13       Impact factor: 4.132

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.