Ciliary: Difference between revisions

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Latest revision as of 07:01, 17 March 2025

Ciliary

The term ciliary refers to structures related to or resembling cilia, which are microscopic, hair-like projections on the surface of certain cells. Cilia play crucial roles in various biological processes, including movement, sensory functions, and the maintenance of fluid flow across cell surfaces.

Types of Cilia[edit]

Cilia can be broadly classified into two types:

  • Motile cilia: These cilia are capable of movement and are primarily involved in locomotion and the movement of fluids over cell surfaces. They are found in large numbers on the surface of certain cells, such as those lining the respiratory tract.
  • Non-motile cilia: Also known as primary cilia, these cilia are typically involved in sensory functions and signal transduction. They are usually present as a single cilium per cell and play a role in various signaling pathways.

Ciliary Structure[edit]

Cilia are composed of a core structure known as the axoneme, which consists of microtubules arranged in a characteristic "9+2" pattern in motile cilia and a "9+0" pattern in non-motile cilia. The axoneme is anchored to the cell by the basal body, which is derived from the centriole.

Ciliary Function[edit]

Cilia perform a variety of functions depending on their type and location:

  • In the respiratory system, motile cilia help to clear mucus and debris from the airways.
  • In the reproductive system, cilia in the fallopian tubes assist in the movement of the egg towards the uterus.
  • Primary cilia are involved in sensing environmental signals and regulating cellular responses.

Ciliary Disorders[edit]

Defects in ciliary structure or function can lead to a group of disorders known as ciliopathies. These include:

  • Primary ciliary dyskinesia: A genetic disorder affecting the motility of cilia, leading to respiratory problems, infertility, and other issues.
  • Polycystic kidney disease: A condition characterized by the formation of cysts in the kidneys, often associated with defects in primary cilia.

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