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Characteristic distribution and molecular properties of normal cellular prion protein in human endocrine and exocrine tissues.


ABSTRACT: Prion disease is an infectious and fatal neurodegenerative disease. Human prion disease autopsy studies have revealed abnormal prion protein (PrPSc) deposits in the central nervous system and systemic organs. In deer, chronic wasting disease has also become a global problem, with PrPSc in saliva and feces. Therefore, understanding normal cellular prion proteins (PrPc) characteristics in human systemic organs is important since they could be a PrPSc source. This study used western blotting and immunohistochemistry to investigate endocrine and exocrine tissues, such as the human pituitary, adrenal, submandibular glands and the pancreas. All tissues had 30-40 kDa PrP signals, which is a slightly higher molecular weight than normal brain tissue. Most

SUBMITTER: Koyama S 

PROVIDER: S-EPMC9464206 | biostudies-literature | 2022 Sep

REPOSITORIES: biostudies-literature