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The Annual Society for Neuroscience (SfN) meeting features the latest discoveries in brain research, from the basic mechanisms to translational and clinical studies. Here are some highlights from the conference.

This year,  the conference celebrated its 50th anniversary in the "Windy City," Chicago, IL, USA. Unsurprisingly, this convention attracted close to 30,000 delegates around the workings of the brain, "the universe between your ears" unassuming but possibly, the most complex structure of the universe.


A zoo of brains

We must humbly acknowledge that much of what we know about the structure and function of the human brain today has been extrapolated from decades of studies on rodent models, lower vertebrates, and indeed, even invertebrate nervous systems. The 50th SfN reported on a "zoo" of Daphnias, inebriated fruit flies, severed zebrafish spinal cords, and RNAi-knocked roundworms, having had specific populations of their limited subset of neurons knocked out by RNAi.

"I think; therefore I am?"

The purpose and function of the brain have kept philosophers busy for hundreds of years. We live in fascinating times where we can finally design and make the tools and skills to embark on the global mapping of the detailed molecular identity and projections of every single neuron and glial cell in the human brain.

Overwhelmed by complex data sets, we are now in a state of ordered confusion and, at best, a fragmented knowledge about how the brain wires and connects the "connectome." Still, we cannot define consciousness without referring to metaphysical metaphors, like Christof Koch at Allen Brain Atlas. He supports a reductionist view, simply stating that consciousness can be confined to a limited circuit of neurons in the brain. It is a fascinating prospect that the neuroanatomists Golgi and Cajal at the turn of the 20th century, thought they had it all figured out by showing their ingenious silver impregnation methods able for the first time to discern sub-cellular details about the normal and pathological micro-anatomy of the brain.

The main conundrum of that day was whether the neurons were continuous or interconnected by what we today define as synaptic contacts. However, it is self-evident that it is not enough to know how single neurons work and fire together in isolation to understand the matter that builds up our minds.


The neuronal mosaic

As it has turned out, neurons exhibit striking and stochastic cellular diversity. How is this diversity generated? This is exceedingly difficult to study since neurons are diverse, subtypes intermingled, and fail to divide, plus the fact that single-cell approaches have limited resolution.

The frequent occurrence in the human brain of "brain only" somatic mutations absent from blood DNA may surprise most and may occur from the first cell division till the last. Single-cell genomes can differ by hundreds of mutations from one neuron to the next neighboring nerve cell, causing somatic "mosaicism."

Autistic Spectrum Disorder, ASD shows excess mutation frequency in critical exons of genes expressed in the early brain compared to normal siblings. De novo somatic mosaicism occurs in neuropsychiatric disorders, as can be exemplified by the somatic activation of the AKT3-mTOR pathway causing hemispheric developmental brain malformations.


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Gene therapy of the brain

The application of gene therapies to correct peripheral disorders like cystic fibrosis or blood cancers is rather familiar, whereas tinkering with the genome of the CNS may sound a little like science fiction.

On the contrary, it now seems that the development of novel vectors and a growing understanding of how to administrate and disseminate these vectors in vivo have opened up entirely new possibilities to address genetic diseases of the brain otherwise unattainable by classical pharmacotherapy.

Gene therapies allow the removal of faulty or misexpressed proteins from the brain parenchyma by targeting mutated alleles. Lysosomal storage diseases are excellent target ailments exemplifying their use. In such diseases, progressive intracellular deposition of lysosomal substrates within lysosomes is the prime cause of cell death.

Microglia! the rising star(s)

One of the cell types that received a particularly hearty welcome at this year's SfN summit was the microglia, the resident immune cells of the CNS, with a particular aptitude to adjust to microenvironmental changes.

These cells are multitasking, including tidying up debris, pruning of synapses, and regulating injury response after demyelination of the brain. By analyzing thousands of individual isolated microglia using distinct sets of biomarkers, nine different microglial activation states have been identified in the mouse brain. The so-called reactive microglia are intimately involved in demyelinating brain diseases, including human multiple sclerosis (MS) lesions.

Scientific dispute? Details matter!

Scientific candor and courage to share information are essential in the scientific world and nourish scientific progress. A perfect example of this was the "dual" (not a duel!) concerned with the controversy about neurogenesis: does it occur in the adult hippocampus or not? Where Dr. Alvarez-Buylla failed to find any traces of young neurons, Dr. LLorens-Martin declares an opposite view, claiming that low-hippocampal neurogenesis continues, albeit at a low frequency, into the 9th decade of life in humans, persisting throughout physiological and pathological aging.

The discrepancy in their views is likely accounted for by methodological differences in the analyses of the brain tissues regarding tissue fixation and antigen retrieval.

This was just a minimal teaser of what took place on the shore of Lake Michigan; the rest not accounted for here was just as interesting.