Summary: Microglia do not only remove damaged materials following a seizure, they also appear to heal damaged neurons.
Source: University of Virginia
University of Virginia School of Medicine researchers have discovered a previously unknown repair process in the brain that they hope could be harnessed and enhanced to treat seizure-related brain injuries.
Common seizure-preventing drugs do not work for approximately a third of epilepsy patients, so new and better treatments for such brain injuries are much needed. UVA’s discovery identifies a potential avenue, one inspired by the brain’s natural immune response.
Using high-powered imaging, the researchers were able to see, for the first time, that immune cells called microglia were not just removing damaged material after experimental seizures but actually appeared to be healing damaged neurons.
“There has been mounting generic support for the idea that microglia could be used to ameliorate seizures, but direct, visualized evidence for how they could do this has been lacking,” said researcher Ukpong B. Eyo, PhD, of UVA’s Department of Neuroscience, the UVA Brain Institute and UVA’s Center for Brain Immunology and Glia (BIG). “Our results indicate that microglia may not be simply clearing debris but providing structural support for neuronal integrity that may have implications even beyond the scope of seizures and epilepsy.”
A Surprising Response to Seizures
The new findings come from a collaboration of scientists at UVA, Mayo Clinic and Rutgers University. They used an advanced imaging technique called two-photon microscopy to examine what happened in the brains of lab mice after severe seizures. What they saw was strange and unexpected.
Rather than simply cleaning up debris, the microglia began forming pouches. These pouches didn’t swallow up damaged material, as many immune cells do. Instead, they began tending to swollen dendrites – the branches of nerve cells that transmit nerve impulses. They weren’t removing, the scientists realized; they appeared to be healing.
These odd little pouches – the scientists named them “microglial process pouches” – stuck around for hours. They often shrank, but they were clearly doing something beneficial because the dendrites they targeted ended up looking better and healthier than those they didn’t.
“We did not find microglia to be ‘eating’ the neuronal elements in this context,” Eyo said. “Rather, we saw a strong correlation between these interactions and a structural resolution of injured neurons suggestive of a ‘healing’ process.”
The new insights into the brain’s immune response points scientists in promising new directions. “Although these findings are exciting, there is yet a lot to follow-up on them. For example, the precise mechanisms that regulate the interactions remain to be identified. Moreover, at present, the ‘healing’ feature is suggested from correlational results and more definitive studies are required to certify the nature of the ‘healing,'” Eyo said. “If these questions can be answered, they will provide a rationale for developing approaches to enhance this process … in seizure contexts.”
Eyo has already received two grants totaling almost $5 million from the National Institutes of Health to continue his study of microglia. The funding will allow him to study how the immune cells help regulate vascular function, which could be important in diseases such as Alzheimer’s, and their role in brain-hyperactivity disorders such as febrile seizures that can trigger epilepsy.
“With this new funding, we are eager to clarify roles for microglia in seizure disorders and vascular function,” he said. “UVA’s continued investment is neuroscience research provides a suitable home for our lab’s research.”
The researchers have published their findings in the scientific journal Cell Reports. The research team consisted of Eyo, Koichiro Haruwaka, Mingshu Mo, Antony Brayan Campos-Salazar, Lingxiao Wang, Xenophon S. Speros IV, Sruchika Sabu, Pingyi Xu and Long-Jun Wu.
Funding: The research was supported by National Institutes of Health grants R01NS088627, R01NS112144 and K22N84392. Eyo’s new NIH grants are R01NS119243 and R01NS122782
About this epilepsy research news
Source: University of Virginia
Contact: Josh Barney – University of Virginia
Image: The image is in the public domain
Original Research: Open access.
“Microglia provide structural resolution to injured dendrites after severe seizures” by Ukpong B. Eyo et al. Current Biology
Microglia provide structural resolution to injured dendrites after severe seizures
- •Cortical microglia form process pouches following severe experimental seizures
- •Microglial process pouches target beaded dendrites following severe seizures
- •Microglial process pouches are long lived with little evidence for phagocytosis
- •Microglial process pouches correlate with the structural resolution of dendrites
Although an imbalance between neuronal excitation and inhibition underlies seizures, clinical approaches that target these mechanisms are insufficient in containing seizures in patients with epilepsy, raising the need for alternative approaches. Brain-resident microglia contribute to the development and stability of neuronal structure and functional networks that are perturbed during seizures.
However, the extent of microglial contributions in response to seizures in vivo remain to be elucidated. Using two-photon in vivo imaging to visualize microglial dynamics, we show that severe seizures induce formation of microglial process pouches that target but rarely engulf beaded neuronal dendrites.
Microglial process pouches are stable for hours, although they often shrink in size. We further find that microglial process pouches are associated with a better structural resolution of beaded dendrites.
These findings provide evidence for the structural resolution of injured dendrites by microglia as a form of neuroprotection.