A Protein Associated with Toll-Like Receptor 4 (PRAT4A) Regulates Cell Surface Expression of TLR4

Yasutaka Wakabayashi(University of Tokyo Hospital), Makiko Kobayashi(University of Tokyo Hospital), Sachiko Akashi‐Takamura(University of Tokyo Hospital), Natsuko Tanimura(University of Tokyo Hospital), Kazunori Konno(University of Tokyo Hospital), Koichiro Takahashi(University of Tokyo Hospital), Takashi Ishii(University of Tokyo Hospital), Taketoshi Mizutani(Interaction Design (United Kingdom)), Hideo Iba(Interaction Design (United Kingdom)), Taku Kouro(Tokyo Medical University), Satoshi Takaki(Tokyo Medical University), Kiyoshi Takatsu(Tokyo Medical University), Yoshiya Oda(Eisai (Japan)), Yasushi Ishihama(Eisai (Japan)), Shin-ichiroh Saitoh(University of Tokyo Hospital), Kensuke Miyake(Japan Science and Technology Agency)
The Journal of Immunology
August 1, 2006
Cited by 108Open Access
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Abstract

TLRs recognize microbial products. Their subcellular distribution is optimized for microbial recognition. Little is known, however, about mechanisms regulating the subcellular distribution of TLRs. LPS is recognized by the receptor complex consisting of TLR4 and MD-2. Although MD-2, a coreceptor for TLR4, enhances cell surface expression of TLR4, an additional mechanism regulating TLR4 distribution has been suggested. We show here that PRAT4A, a novel protein associated with TLR4, regulates cell surface expression of TLR4. PRAT4A is associated with the immature form of TLR4 but not with MD-2 or TLR2. PRAT4A knockdown abolished LPS responsiveness in a cell line expressing TLR4/MD-2, probably due to the lack of cell surface TLR4. PRAT4A knockdown down-regulated cell surface TLR4/MD-2 on dendritic cells. These results demonstrate a novel mechanism regulating TLR4/MD-2 expression on the cell surface.


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