Lung Disease and Melanoma: a Common Molecular Mechanism?
News Sep 02, 2013
Scientists have identified the first known pathway by which their cellular functions turn abnormal, and a healthy process goes haywire. The study is published in Cell Reports.
The team focused on an ancient gene family known as “18 glycosyl hydrolase (GH 18),” and in particular, one protein known as chitinase 3-like-1 (Chi3l1). This protein plays a critical role in the body’s response to foreign pathogens, augmenting the killing of bacteria while controlling inflammation and cell death to keep the immune response from harming normal tissue.
Although previous studies from this Yale team and colleagues have helped define the roles of Chi3l1 in biology, the mechanism by which it works — and triggers disease when overexpressed — was not known. The Yale team knew that Chi3l1 was not functioning as an enzyme would. They theorized that it acted, instead, by binding to a cellular receptor. Their studies led them to focus on a receptor known as IL-13Rα2, which was thought to be a so-called “decoy receptor” that binds molecules but does not induce cellular signaling or activate a biologic response.
Their experiments in mice proved that IL-13Rα2 was no decoy at all, but an active participant in the signaling pathway. The binding of overexpressed Chi3l1 and the receptor IL-13Rα2 began a cascade of subsequent reactions in the mice that resulted in lung disease, lung melanoma metastasis, and a host of other diseases.
“What we discovered was that when Chi3l1 is produced, IL-13Rα2 binds it and acts as a catalyst, triggering important biologic responses such as the control of cell death and production of inflammatory mediators,” said senior author Dr. Jack A. Elias, chair of internal medicine at Yale School of Medicine and a member of Yale Cancer Center.
Elias hopes that further research will identify more receptors in this family, and he sees a potential for developing therapies based on his team’s findings. “These molecules are expressed abnormally in a number of diseases, so the idea that you can control them is exciting. Perhaps we can develop an antibody or a small molecule that blocks their action and changes cellular function.”
Mechanism Controlling Multiple Sclerosis Risk IdentifiedNews
Researchers at Karolinska Institutet have now discovered a new mechanism of a major risk gene for multiple sclerosis (MS) that triggers disease through so-called epigenetic regulation. They also found a protective genetic variant that reduces the risk for MS through the same mechanism.
Synthetic DNA Shuffling Enzyme Outpaces Natural CounterpartNews
A new synthetic enzyme, crafted from DNA rather than protein, flips lipid molecules within the cell membrane, triggering a signal pathway that could be harnessed to induce cell death in cancer cells. Researchers say their lipid-scrambling DNA enzyme is the first in its class to outperform naturally occurring enzymes – and does so by three orders of magnitudeREAD MORE
Antarctic Worm and Machine Learning Help Identify Cerebral Palsy EarlierNews
A research team has released a study in the peer-reviewed journal BMC Bioinformatics showing that DNA methylation patterns in circulating blood cells can be used to help identify spastic cerebral palsy (CP) patients. The technique which makes use of machine learning, data science and even analysis of Antarctic worms, raises hopes for earlier targeted CP therapies.