Syndicate content

Archive - Mar 19, 2018


Scientists Discover New Causes of Cellular Decline in Prematurely Aging Children (Progeria); Finding May Shed Light on Normal Aging

In a paper published in the February 20, 2018 issue of Cell Reports, Saint Louis University researchers have uncovered new answers about why cells age in children with a rare and fatal disease, Hutchinson-Gilford Progeria Syndrome (HGPS). The open-access article is titled “A Cell-Intrinsic Interferon-like Response Links Replication Stress to Cellular Aging Caused by Progerin.” The data points to cellular replication stress and a mistaken innate immune response as culprits, and the team found success in the laboratory in blocking these processes with vitamin D. Susana Gonzalo, PhD, Associate Professor of Biochemistry and Molecular Biology at SLU, and her lab examined human and animal cells connected to HGPS. HGPS is caused by the random mutation of a single gene that causes children to age rapidly. Children with the condition develop many of the typical changes and illness associated with aging, including hair loss, aging skin, joint abnormalities, and bone loss. The disease causes atherosclerosis -- fatty deposits that clog arteries -- and patients with the illness die from cardiovascular complications such as stroke or myocardial infarction in their teens. Thanks to genetic mapping, scientists now know that HGPS is caused by a mutation in the LMNA gene, which encodes the lamin A protein. Lamin A serves as a scaffold that keeps the cell's nucleus organized and in shape. The shortened, mutated version of this protein is called progerin, and it causes the nucleus and cell to become unstable, leading to premature aging of the cells. "Those with progeria have a mutation in their DNA that codes for these proteins," Dr. Gonzalo said. "The presence of progerin makes a mess in the nucleus." This is a problem because the nucleus houses our DNA.

Termite Queen, King Recognition Pheromone Identified

Researchers at North Carolina (NC) State University have, for the first time, identified a specific chemical used by the higher termite castes -- the queens and the kings -- to communicate their royal status with worker termites. The findings could advance knowledge of termite evolution, behavior, and control. A study published online on March 19, 2018 in PNAS shows that a wax-like hydrocarbon -- a chemical consisting of only carbon and hydrogen atoms called heneicosane -- on the body surface of subterranean royal termites is used to enable worker termites to recognize and care for them. The open-access article is titled “"Identification of a Queen and King Recognition Pheromone in the Subterranean Termite Reticulitermes flavipes.” Termites live mostly underground or in wood and are generally blind, necessitating the use of chemical signals to communicate. "This is the first report of a queen recognition pheromone in termites and the first report of a king recognition pheromone in insects," said Coby Schal, PhD, the Blanton J. Whitmire Distinguished Professor of Entomology at NC State. Dr. Schal and NC State Ph.D. graduate Colin Funaro, the paper's co-corresponding authors, used gas chromatography to isolate specific chemicals from the exoskeletons of royal and worker Reticulitermes flavipes termites and found heneicosane on the royal termites, but not on workers. When heneicosane was placed on glass dummies serving as royal termite proxies, workers did not bow or curtsy, but instead started shaking -- an action that seemed to reflect the termite version of royal recognition. Workers shook even more when the royal pheromone was blended with other hydrocarbons from the colony's workers that represent the colony's odor.