So did you ever wonder what happens to the tadpole’s tail? Does it just fall off? No actually. Lysosomes eat it. (autophagy: the cell’s ability to eat itself…) And the webbing in our fingers and toes as fetus’s. Eaten by lysosomes.
This is a great, short and extremely informative piece on these tiny little organelles that are so important to our well-being.
Is the lysosome the first place we should look when we have issues in the body? Not the last? Hmmmm…
The following article was released today by Dr. John Hopwood, who also sits on the International Scientific Advisory Board of the Hide & Seek Foundation. I find it to be the first article that I have read, that I haven’t written, to accurately address the issue of Lysosomal Disease today, as it affects us all. Each and every one of us has lysosomes, and if there is any problem at all within this ultra important organelle, the result can be any number of the most common human (and animal) conditions known to us. It is absolutely time to pay attention.
- Stephanie
Cell malfunction linked to many diseases
Danny Rose
May 21, 2009 – 1:04AM
The tiny “recycling unit” at the core of every human cell can fail, and research is increasingly placing this malfunction at the root of a host of common deadly illnesses.
Alzheimer’s disease, stroke, heart disease and certain cancers can all be linked to a dysfunction of the lysosome, says South Australian biochemical geneticist Professor John Hopwood.
“You might think these lysosomal diseases are uncommon but in fact we’ve been studying the tip of an iceberg,” Prof Hopwood says.
“The more we study these disorders … it turns out the lysosome has a big role to play in many illnesses that the community has.”
Lysosomal disease is a process which sees affected human cells lose their ability to create new versions of themselves, instead becoming clogged as genetic “material gets into the recycler but can’t get out”, Prof Hopwood explains.
His team at Adelaide’s Women’s and Children’s Hospital led the development of world-first treatments for two rare lysosomal diseases – Maroteaux-Lamy and Hunter syndromes.
These and other Lysosomal disease occur in one in every thousand children and it results in developmental delays, bone deformities, heart and breathing difficulties, behavioural problems and a shortened life span.
Prof Hopwood has also developed a test able to highlight these genetic conditions in newborns, allowing treatment to get underway before irreversible features develop.
While his work has focused on treating children with these rare conditions, Prof Hopwood says the field’s future would also go to unearthing the links between lysosomal disorders and common diseases.
In the brain, the disorder was known to lead to the loss of brain matter which, over time, could manifest as Alzheimer’s or dementia.
“Where you have heart failure because a valve doesn’t function properly, it may be due to poor signalling by control systems that are influenced by these lysosomal storage disease problems,” Prof Hopwood says.
“So these rare diseases give us an insight into the ‘berg’ part of the ‘iceberg’, which is affecting the majority of us.
“And if we can understand how it contributes then we can reduce the impact of all of these disorders in the community.”
The Australian Academy of Technological Sciences and Engineering (ATSE) paid tribute to Prof Hopwood for his 25 years work in the field at a gala event in Sydney on Wednesday night.
He was announced as one of the recipients of a 2009 ATSE Clunies Ross Award, which recognises the nation’s pre-eminent scientists who have bridged the gap between research and the marketplace.