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General interest items edited by Janice Flahiff

[Press release] Why Scientists Are Blaming Cilia for Human Disease – Scientific American

Why Scientists Are Blaming Cilia for Human Disease – Scientific American.

Hairlike structures on cells may play a role in a host of genetic disorders, including kidney degeneration, vision impairment and even some cancers

Hairlike cilia may be at the roots of of several genetic disorders.
Image Courtesy of StudyBlue.com

Scientists now believe that a number of genetic disorders, from polycystic kidney disease to some forms of retinal degeneration, can ultimately be traced back to cilia—bristly, hairlike structures that dot cell surfaces.

In a review article published in the December 1 BioScience, George B. Witman, a cellular biologist at the University of Massachusetts Medical School, highlighted the growing body of evidence that abnormal or absent cilia can cause a wide range of human disorders, dubbed “ciliopathies.”

“Kidney disease and blindness, multiple digits, shortened bones or extremities, obesity—all of these things, it turns out, are due to defects in cilia,” he says. Experts add that the discovery of a common thread between these disparate disorders may eventually help researchers develop gene-based therapies to combat those conditions.

At first blush, cilia seem relatively innocuous. As they beat back and forth outside the cell, coordinated brushes of so-called motile cilia regulate fluid flow nearby. But almost all human cells also have one primary, or nonmotile, cilium that functions more like a molecular antenna. The primary cilium is an internally dynamic structure, packed with proteins that detect and convey important messages to its cell about the local environment. “The signaling machinery is concentrated in the cilia,” Witman says. “All in this very tightly controlled, constrained space.”

December 12, 2014 Posted by | Medical and Health Research News | , , , , , , , , , , , | Leave a comment

[News article] Ciliopathies lie behind many human diseases — ScienceDaily

Ciliopathies lie behind many human diseases — ScienceDaily.

Excerpt

Date:December 1, 2014
Source: American Institute of Biological Sciences
Summary: Growing interest in cilia, which are finger-like organelles that extend from the bodies of individual cells, has revealed their role in a number of human ailments. As a result of cilia’s presence in a wide variety of cells, defects in them cause diverse human diseases that warrant further study.

Cilia perform a broad range of functions, including a starring role in cell signalling. Motile ones wiggle and so move fluids within the body, including cerebrospinal fluid in the brain. In humans, cilia are found on almost every cell in the body. Because of this, ciliopathies often make themselves known as syndromes with widely varying effects on a number of tissue types. For instance, the ciliopathy Jeune asphyxiating thoracic dystrophy involves the development of abnormally short ribs, accompanied by short limbs and, occasionally, the development of extra digits.

In primary ciliary dyskinesia, motile cilia are dysfunctional and fail to beat. This can lead to bronchitis resulting from the failure to clear mucus from the sufferer’s airways. Male patients with primary ciliary dyskinesia are infertile because of impaired motility of the sperm’s flagellum (flagella and cilia are structurally similar).

The article’s authors point to a number of other human diseases in which cilia may play a role; for example, some cancers and neurological diseases may be related to ciliopathies. Because of the limitations placed on research involving humans, the authors propose the use of model species ranging from the green alga Chlamydomonas to the house mouse to further study the role of cilia. They write, “We can anticipate that new and improved techniques will open new avenues for gaining further insight into these immensely important and ever more fascinating cell organelles.”

December 5, 2014 Posted by | Medical and Health Research News | , , , , , , , , | Leave a comment

Human Lungs Brush out Intruders

 

From the 23 August 2012 article at ScienceNewsDaily

 A runny nose and a wet cough caused by a cold or an allergy may not feel very good. But human airways rely on sticky mucus to expel foreign matter, including toxic and infectious agents, from the body.Now, a study by Brian Button and colleagues from the University of North Carolina at Chapel Hill, NC, helps to explain how human airways clear such mucus out of the lungs. The findings may give researchers a better understanding of what goes wrong in many human lung diseases, such as cystic fibrosis (CF), chronic obstructive pulmonary disease (COPD) and asthma.

The researchers’ report appears in the 24 August issue of the journalScience.

“The air we breathe isn’t exactly clean, and we take in many dangerous elements with every breath,” explains Michael Rubinstein, a co-author of the Science report. “We need a mechanism to remove all the junk we breathe in, and the way it’s done is with a very sticky gel called mucus that catches these particles and removes them with the help of tiny cilia.”

“The cilia are constantly beating, even while we sleep,” he says. “In a coordinated fashion, they push mucus containing foreign objects out of the lungs, and we either swallow it or spit it out. These cilia even beat for a few hours after we die. If they stopped, we’d be flooded with mucus that provides a fertile breeding ground for bacteria.”

Until now, most researchers have subscribed to a “gel-on-liquid” model of mucus clearance, in which a watery “periciliary” layer acts as a lubricant and separates mucus from epithelial cells that line human airways. But this old explanation fails to explain how mucus remains in its own distinct layer.

“We can’t have a watery layer separating sticky mucus from our cells because there is an osmotic pressure in the mucus that causes it to expand in water,” Rubinstein says. “So what is really keeping the mucus from sticking to our cells?”

The researchers used a combination of imaging techniques to observe a dense meshwork in the periciliary layer of human bronchial epithelial cell cultures. The brush-like layer consists of protective molecules that keep sticky mucus from reaching the cilia and epithelial cells, thus ensuring the normal flow of mucus.

Based on their findings, Button and the other researchers propose a “gel-on-brush” form of mucus clearance in which mucus moves atop a brush-like periciliary layer instead of a watery one. They suggest that this mechanism captures the physics of human mucus clearance more accurately.

“This layer — this brush — seems to be very important for the healthy functioning of human airways,” according to Rubinstein. “It protects cells from sticky mucus, and it creates a second barrier of defense in case viruses or bacteria penetrate through the mucus. They would not penetrate through the brush layer because the brush is denser.”

“We found that there is a specific condition, below which the brush is healthy and cells are happy,” Rubinstein explains. “But above this ideal condition, in diseases like CF or COPD, the brush becomes compressed and actually prevents the normal cilia beating and healthy flow of mucus.”

The researchers explain that, whenever the mucus layer gets too dense, it can crash through the periciliary brush, collapse the cilia and stick to the cell surface.

“The collapse of this brush is what can lead to immobile mucus and result in infection, inflammation and eventually the destruction of lung tissue and the loss of lung function,” says Rubinstein. “But our new model should guide researchers to develop novel therapies to treat lung diseases and provide them with biomarkers to track the effectiveness of those therapies.”

 

 

August 27, 2012 Posted by | Uncategorized | , , , , , | Leave a comment

   

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