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Some motile cilia lack the central pair, and some non-motile cilia have the central pair, hence the four types. [5] [7] Most non-motile cilia, termed primary cilia or sensory cilia, serve solely as sensory organelles. [8] [9] Most vertebrate cell types possess a single non-motile primary cilium, which functions as a cellular antenna.
Cilia occur in all members of the group (although the peculiar Suctoria only have them for part of their life cycle) and are variously used in swimming, crawling, attachment, feeding, and sensation. Ciliates are an important group of protists , common almost anywhere there is water—in lakes, ponds, oceans, rivers, and soils, including anoxic ...
The MTOC reorients itself during signal transduction, primarily during wound repair or immune responses. [5] The MTOC is relocalized to a position between the edge of the cell and the nucleus in cells like macrophages, fibroblasts, and endothelial cells. Organelles like the Golgi apparatus aid in the reorientation of the MTOC which can occur ...
Cilia Structure. Primary cilia are found to be formed when a cell exits the cell cycle. [2] Cilia consist of four main compartments: the basal body at the base, the transition zone, the axenome which is an arrangement of nine doublet microtubules and considered to be the core of the cilium, and the ciliary membrane. [2]
The flagellar axoneme itself is a bundle of nine pairs of microtubule doublets surrounding two central microtubules, termed the 9+2 axoneme, [10] and cross-linking dynein motors, powered by ATP hydrolysis, perform mechanical work by promoting the relative sliding of filaments, resulting in bending deformations.
A ciliopathy is any genetic disorder that affects the cellular cilia or the cilia anchoring structures, the basal bodies, [1] or ciliary function. [2] Primary cilia are important in guiding the process of development, so abnormal ciliary function while an embryo is developing can lead to a set of malformations that can occur regardless of the particular genetic problem. [3]
Primary ciliary dyskinesia (PCD) is a rare, autosomal recessive genetic ciliopathy, that causes defects in the action of cilia lining the upper and lower respiratory tract, sinuses, Eustachian tube, middle ear, fallopian tube, and flagella of sperm cells.
Intraflagellar transport in the cilia of the nematode C. elegans. Intraflagellar transport (IFT) is a bidirectional motility along axoneme microtubules that is essential for the formation (ciliogenesis) and maintenance of most eukaryotic cilia and flagella. [1]