Results 11 to 20 of about 18,298 (255)

Ciliogenesis membrane dynamics and organization

open access: hybridSeminars in Cell & Developmental Biology, 2022
Ciliogenesis is a complex multistep process used to describe assembly of cilia and flagella. These organelles play essential roles in motility and signaling on the surface of cells. Cilia are built at the distal ends of centrioles through the formation of an axoneme that is surrounded by the ciliary membrane.
Huijie Zhao   +2 more
openalex   +3 more sources

TRIP6 functions in brain ciliogenesis [PDF]

open access: yesNature Communications, 2021
AbstractTRIP6, a member of the ZYXIN-family of LIM domain proteins, is a focal adhesion component.Trip6deletion in the mouse, reported here, reveals a function in the brain: ependymal and choroid plexus epithelial cells are carrying, unexpectedly, fewer and shorter cilia, are poorly differentiated, and the mice develop hydrocephalus.
Shalmali Shukla   +13 more
openaire   +7 more sources

Autophagy and Ciliogenesis

open access: yesJMA Journal, 2021
Autophagy is a major intracellular degradation system and plays important roles in various physiological processes such as metabolic adaptation and intracellular homeostasis. It degrades intracellular components both randomly and selectively. Autophagic activity is tightly regulated primarily by nutrient availability, but also by other extracellular ...
Yamamoto, Yasuhiro, Mizushima, Noboru
openaire   +2 more sources

Ciliogenesis and the DNA damage response: a stressful relationship [PDF]

open access: hybrid, 2016
Both inherited and sporadic mutations can give rise to a plethora of human diseases. Through myriad diverse cellular processes, sporadic mutations can arise through a failure to accurately replicate the genetic code or by inaccurate separation of ...
Colin A. Johnson, Spencer J. Collis
openalex   +6 more sources

Mechanobiology of Ciliogenesis [PDF]

open access: yesBioScience, 2014
Cilia are force-generating and -sensing organelles that serve as mechanical interfaces between the cell and the extracellular environment. Cilia are present in tissues that adaptively respond to mechanical loading and fluid flow, and defects in ciliary function can lead to diseases affecting these tissues.
Ishikawa, Hiroaki, Marshall, Wallace F
openaire   +4 more sources

CCP5 and CCP6 retain CP110 and negatively regulate ciliogenesis

open access: yesBMC Biology, 2023
Background The axonemal microtubules of primary cilium undergo a conserved protein posttranslational modification (PTM) — polyglutamylation. This reversible procedure is processed by tubulin tyrosine ligase-like polyglutamylases to form secondary ...
Yujuan Wang   +6 more
doaj   +1 more source

Centriolar satellites expedite mother centriole remodeling to promote ciliogenesis

open access: yeseLife, 2023
Centrosomes are orbited by centriolar satellites, dynamic multiprotein assemblies nucleated by Pericentriolar material 1 (PCM1). To study the requirement for centriolar satellites, we generated mice lacking PCM1, a crucial component of satellites. Pcm1−/−
Emma A Hall   +18 more
doaj   +1 more source

Enhanced primary ciliogenesis via mitochondrial oxidative stress activates AKT to prevent neurotoxicity in HSPA9/mortalin-depleted SH-SY5Y cells

open access: yesMolecular Brain, 2023
The primary cilium, an antenna-like structure on the cell surface, acts as a mechanical and chemical sensory organelle. Primary cilia play critical roles in sensing the extracellular environment to coordinate various developmental and homeostatic ...
Ji-Eun Bae   +17 more
doaj   +1 more source

Centrobin controls primary ciliogenesis in vertebrates [PDF]

open access: bronzeJournal of Cell Biology, 2018
The BRCA2 interactor, centrobin, is a centrosomal protein that has been implicated in centriole duplication and microtubule stability. We used genome editing to ablate CNTROB in hTERT-RPE1 cells and observed an increased frequency of monocentriolar and acentriolar cells.
Yetunde Adesanya Ogungbenro   +6 more
openalex   +5 more sources

A meckelin–filamin A interaction mediates ciliogenesis [PDF]

open access: yesHuman Molecular Genetics, 2011
MKS3, encoding the transmembrane receptor meckelin, is mutated in Meckel-Gruber syndrome (MKS), an autosomal-recessive ciliopathy. Meckelin localizes to the primary cilium, basal body and elsewhere within the cell. Here, we found that the cytoplasmic domain of meckelin directly interacts with the actin-binding protein filamin A, potentially at the ...
Adams, M.   +13 more
openaire   +4 more sources

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