Sugaya Makoto, Nakamura Koichiro, Watanabe Takahiro, Asahina Akihiko, Yasaka Nami, Koyama Yoh ichi, Kusubata Masashi, Ushiki Yuko, Kimura Kumiko, Morooka Akira, Irie Shinkichi, Yokoyama Takashi, Inoue Keiichi, Itohara Shigeyosi, Tamaki Kunihiko
Faculty of Medicine, Department of Dermatology, University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, 113-8655, Tokyo, Japan.
J Dermatol Sci. 2002 Feb;28(2):126-34. doi: 10.1016/s0923-1811(01)00160-8.
Transmissible spongiform encephalopathies are characterized by the accumulation of a proteinase-resistant isoform of the cellular prion-related protein (PrP(c)) within the central nervous system (CNS). The accumulation of scrapie-associated PrP (PrP(Sc)) within cells of the lymphoreticular system prior to its accumulation in the CNS is regarded as important for the development of neurological diseases after peripheral inoculation. Little, however, is known as to which cells are the targets for peripheral inoculation. Here, the presence of PrP(c) on murine Langerhans cells (LC), dendritic cells in the skin and mucosa, and keratinocytes (KC) is demonstrated by immunohistochemical staining, Western-blotting and FACS analysis. The expression of PrP(c) mRNA in freshly purified LC and KC was also detected by reverse transcriptase-polymerase chain reaction. The expression of PrP(c) on LC was slightly increased during culture. These data suggest that LC and KC may be the targets for peripheral infection with prions.