Since 2012, the number of humanities majors has plunged as students chased degrees with what looked like guaranteed career payoffs. But the job market has changed.
An unexpected and potentially big finding:
A single mitochondrial protein has an outsized role, acting as a central node, coordinating our circadian clock, temperature, dietary cues, sleep/wake cycle to control brown fat metabolism.
Brown/beige fat burns energy to keep the body warm and is linked to metabolic health. Its activity follows a daily rhythm (high when you’re awake, low during sleep), but it can also ramp up *suddenly* in response to cold weather or a fatty meal. How one system handles both scheduled and surprise demands was a mystery — until now.
The answer: one mitochondrial protein, SLC25A34.
The researchers found that three different signals — the circadian clock, diet, and temperature — all funnel through a single orphan mitochondrial transporter called SLC25A34.
How it works:
- During sleep: The circadian clock proteins REV-ERBα/β shut off SLC25A34 production.
“A lot of the previous work in this area has been epidemiological in nature, without much focus on the molecular mechanisms that actually underpin the connection between infections and ALS,” says Ahmed, who co-first authored the new paper with Miller Lab alumni Art Marzok and Jonathan Mapletoft. “What makes our study unique is that we did take a mechanistic approach — we explored why this connection might exist.”
What the researchers found was that even common respiratory viruses that do not infect neurons can leave lasting changes to the nervous system.
In their animal models, Miller’s team observed that COVID-19 and flu infections triggered an inflammatory response from immune cells in the nervous system — a process called gliosis — that remained elevated in the spinal cord even after the virus had been cleared from the body. Gliosis, Ahmed notes, is already known to play an important role in ALS, but the findings suggest that an infection may amplify this process, helping to accelerate the disease.
A research consortium has generated the broadest look yet at the proteins that make up mitochondria, capturing the organelle’s diversity across multiple branches on the tree of complex life. With major contributions from Broad Institute scientists and its Proteomics Platform, the consortium generated and analyzed the mitochondrial proteomes of one plant and five single-celled pathogens that affect millions of people globally every year.
Their results reveal unexpected functions of the organelle, clues to its origin and role in the evolution of complex-celled organisms known as eukaryotes, and potential new drug targets for neglected tropical diseases.
The MitoCarta Tree of Life project was led by scientists at the Broad Institute, Mass General Brigham, Harvard Medical School (HMS), Harvard T.H. Chan School of Public Health, and Boston University Henry M. Goldman School of Dental Medicine. Their findings appear in nine scientific papers and a commentary article in Cell and related journals.
Canada is moving to expand its role in supplying nuclear isotopes that could power spacecraft on long-duration missions.
The Nuclear Innovation Institute launched the Canadian Centre for Space Isotopes this week in Toronto. The organization will focus on research, policy, and partnerships across the nuclear and space industries.
Radioisotope power systems convert heat from radioactive decay into electricity. They provide steady power without relying on sunlight, making them useful for missions traveling far from the Sun.
On September 22, the Coronagraph Instrument on NASA’s Nancy Grace Roman Space Telescope opened its eyes to cosmic light for the first time. The ultimate purpose of the instrument—which is commanded from Caltech’s IPAC, a science and data center for astrophysics and planetary sciences—is to demonstrate technology that can block starlight, providing unprecedented views of the planets and dusty disks around nearby stars.
The coronagraph first woke up on September 1 and stretched its digital, electronic, and mechanical “limbs” mid-month. Once the Roman team confirmed that the fine-guidance system was holding the Coronagraph Instrument steady, scientists adjusted the focus so it could take its first bleary-eyed look at space, which will help scientists fine-tune the instrument’s view.
“We’re all extremely pleased with how well things are working,” says Alexandra Greenbaum, coronagraph data management system lead at IPAC. “There’s a lot of collaboration that went into this milestone, so it’s wonderful to see all of us working together and to be a part of the team. I’m really looking forward to supporting the rest of commissioning, both on the operations and the data processing.”
Conventional radiotherapy target delineation for glioblastoma (GBM) includes an isotropic expansion from gross tumor visible on anatomic MRI to an empirically defined clinical target volume (CTV) for coverage of microscopic infiltrative disease. GBM spreads preferentially along white matter tracts, but this information has not previously been systematically incorporated into radiotherapy planning. We investigated using white matter tractography from diffusion-weighted MRI (dwMRI) to inform target delineation.
Thirteen patients with GBM underwent 55-directional dwMRI at the time of post-operative radiation planning MRI. Whole-brain tractography was performed, and streamlines passing within 5 mm of gross disease were used to generate maps representing white matter path length from gross disease. Clinical target volumes were generated using tractography (CTVtract) and conventional isotropic expansion (CTVisotropic). MRI at time of GBM recurrence was registered to the radiation planning MRI, and coverage of the recurrence volume was compared between CTVtract and CTVisotropic.
CTVtract demonstrated non-isotropic expansion of the primary tumor along regional white matter tracts while respecting natural anatomic boundaries. CTVtract volumes using a 2 cm path-length were a median of 67 cc smaller (−19%) than the paired 2 cm CTVisotropic volumes (p = 0.003). 10/13 recurrence volumes were included in CTVisotropic, while 12/13 recurrence volumes were included in CTVtract.