Variations in morphology and ion-channel expression largely determine the electrophysiological properties of neurons.

Contrary to what one might imagine, the way in which each of us interacts with the world is not a simple matter of seeing (or touching, or smelling) and then reacting. Even the best baseball hitter eyeing a fastball does not swing at what he sees. The neurons and neural connections that make up our sensory systems are far too slow for this to work.

Brain cells known as neurons process information by joining into complex networks, transmitting signals to each other across junctions called synapses. But “neurons don’t just connect to other neurons,” emphasizes Z. Josh Huang, Ph.D., “in a lot of cases, they connect to very specific partners, at particular spots.”

The developing nervous system makes far more nerve cells than are needed to ensure target organs and tissues are properly connected to the nervous system. As nerves connect to target organs, they somehow compete with each other resulting in some living and some dying.

A new technique that marries a fast-moving laser beam with a special microscope that look at tissues in different optical planes will enable scientists to get a three-dimensional view of neurons or nerve cells as they interact, said Baylor College of Medicine scientists in a report that appears today in the journal Nature Neuroscience.

It's well known that the left and right sides of the brain differ in many animal species and this is thought to influence cognitive performance and social behaviour. For instance, in humans, the left half of the brain is concerned with language processing whereas the right side is better at comprehending musical melody.

Researchers have discovered that neurons can use two different neurotransmitters that target the same receptor on a receiving neuron to shape the transmission of a nerve impulse. Although the researchers’ experiments identified the “co-release” of the two neurotransmitters only in specific types of neurons in the brain’s auditory center, their finding may apply more broadly in the brain, they said.

The human ear is exquisitely tuned to discern different sound frequencies, whether such tones are high or low, near or far. But the ability of our ears pales in comparison to the remarkable knack of single neurons in the brain to distinguish between the very subtlest of sound frequencies.

Most of the attention directed at в-amyloid precursor protein (APP) has focused on its cleavage and its cleavage products, such as Aв, one of the hallmarks of Alzheimer’s disease. However, there are clues that full-length APP has important developmental roles.

Subplate neurons – once thought to die after directing the wiring of the cerebral cortex or gray matter– remain in the white matter of the adult brain in small numbers and maintain activity, communicating with other neurons in the brain said researchers from Baylor College of Medicine and the University of Alabama at Birmingham in a report.

Researchers have long attempted to unravel the cryptic code used by the neurons of the brain to represent our visual world. By studying the way the brain rapidly and precisely encodes natural visual events that occur on a slower timescale, a team of Harvard bioengineers and brain scientists from the State University of New York have moved one step closer towards solving this riddle.

Researchers at the University of Illinois have developed a method for culturing mammalian neurons in chambers not much larger than the neurons themselves. The new approach extends the lifespan of the neurons at very low densities, an essential step toward developing a method for studying the growth and behavior of individual brain cells.