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Structural basis of the Inv compartment and ciliary abnormalities in Inv/nphp2 mutant mice
Author(s) -
Tsuji Takuma,
Matsuo Kazuhiko,
Nakahari Takashi,
Marunaka Yoshinori,
Yokoyama Takahiko
Publication year - 2016
Publication title -
cytoskeleton
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.95
H-Index - 86
eISSN - 1949-3592
pISSN - 1949-3584
DOI - 10.1002/cm.21264
Subject(s) - cilium , axoneme , basal body , biology , microtubule , compartment (ship) , anatomy , microbiology and biotechnology , centriole , mucociliary clearance , nephronophthisis , motile cilium , intraflagellar transport , mutant , flagellum , lung , gene , genetics , medicine , phenotype , oceanography , geology
The primary cilium is a hair like structure protruding from most mammalian cells. The basic design of the primary cilium consists of a nine microtubule doublet structure (the axoneme). The Inv compartment, a distinct proximal segment of the ciliary body, is defined as the region in which the Inv protein is localized. Inv gene is a responsible gene for human nephronophthisis type2 (NPHP2). Here, we show that renal cilia have a short proximal microtubule doublet region and a long distal microtubule singlet region. The length of the Inv compartment was similar to that of the microtubule doublet region, suggesting a possibility that the doublet region is the structural basis of the Inv compartment. Respiratory cilia of inv mouse mutants had ciliary rootlet malformation and showed reduced ciliary beating frequency and ciliary beating angle, which may explain recurrent bronchitis in NPHP2 patients. In multiciliated tracheal cells, most Inv proteins were retained in the basal body and did not accumulate in the Inv compartment. These results suggest that the machinery to transport and retain Inv in cilia is different between renal and tracheal cilia and that Inv may function in the basal body of tracheal cells. © 2015 Wiley Periodicals, Inc.