by Magdalena Kegel
In News
November 29, 2016
Researchers
have found a way to harness inflammation with the help of ultraviolet (UV)
light, making it possible to design an anti-inflammatory treatment that is more
specific and causes fewer side effects.
If this
approach can be developed for clinical treatment, it likely will
have a large impact on the lives of people with multiple sclerosis and other
inflammatory conditions.
The
study, “Chemical optogenetic modulation of inflammation and immunity,” was
published in the journal Chemical
Science.
HDACs
(histone deacetylases) are molecules driving inflammation and controlling a
range of other processes. Drugs that block HDACs are being investigated in
conditions that include neurodegeneration and cancer, but their role in
inflammation is only beginning to be explored.
Since
HDACs exist in tissues throughout the body, a blocker often interrupts other
enzyme actions than the one intended, resulting in unwanted side effects.
To get around the problem, researchers at Cornell University designed a
molecule that can activate a HDAC blocker using UV light.
“Currently,
there aren’t a lot of tools that are able to manipulate the immune system in a
spatio-temporal fashion,” Pamela Chang, an assistant professor of microbiology
and immunology, and the study’s senior author, said in a news release.
The
team used an existing blocker and covered the part of the drug that interacts
with HDAC with an additional molecule. This addition is set lose when the
compound is exposed to UV light, allowing the drug to block HDAC.
“If you
turned off all the HDACs in the body, you would probably be hitting a lot of
pathways that you didn’t want to turn off,” said Chang. “We can control
when and where we turn off the HDACs using light. The idea is that you can
actually target the tissue that has chronic inflammation and regulate it by
selectively inhibiting HDACs in the tissue that’s affected.”
In this
way, the side effects of a treatment can be minimized.
So far,
researchers tested the new compound in lab-grown cells, where UV-triggered drug
actions reduced the levels of inflammatory molecules. The team also showed that
the compound did not harm the cells.
“We are
pushing the forefront of developing new technologies to control inflammation
and the immune system, with the ultimate goal of being able to study these
biological pathways and perhaps develop therapies for inflammatory diseases,”
Chang concluded.
In
support of Multiple Sclerosis (MS) research:
Never
give up!