FeedFeed2CommentsDeliciousDiggFacebookTwitter
Leave a comment.
Campaigns
Sign the petition to remove the umbrella use of the term 'transgender' to cover women of transsexual / intersex history.
Petition: remove women of transsexual / intersex history from the GLAAD Media Reference Guide.
[ link ] Also read Andrea Rosenfield's call for reform here at TS-Si.[ link ]
TS-Si supports open access to publicly funded research.
TS-Si supports open and immediate access to publicly funded research.
Diversions
TS-Si Site News
TS-Si Reboot Gets Underway
Old & New Neurons Select Information Transmission Method Print E-mail
SciMed - Neuroscience
TS-Si News Service   
Sunday, 03 April 2011 15:00
Old & New Neurons Select Information Transmission MethodPittsburg, PA & New Haven, CT, USA. There is a fundamental mechanism used by neurons to communicate despite the brain's noisy environment, whether they are existing brain cells or altogether new adult growth neurons.

Tens of thousands of the billions of neurons in the brain might be trying to send signals to one another at any given time. Much like a person trying to be heard by a friend across a crowded room, individual neurons must select the best way to get their message heard above the noise.


Neurons communicate by sending out electrical impulses called action potentials (or spikes). These spikes code information much like a version of Morse code with only dots and no dashes. However, groups of neurons must solve a universal communications problem and choose to communicate information in one of two ways: by spiking simultaneously or by spiking separately. In essence, they can send short messages that are broadcast across a wide area or speak locally while delivering more complex content.

Neuron Communication

Existing Neuron Communication

Inhibitory circuits in the olfactory bulb use a novel, time-scale dependent strategy to mediate how neurons choose between encoding and propagating information.

The research was conducted at the Center for the Neural Basis of Cognition, a joint program between Carnegie Mellon University and the University of Pittsburgh.

The findings appear in the Proceedings of the National Academy of Sciences (PNAS). [C1]

New Neuron Communication

New Neuron Communication

Scientists from the Yale School of Medicine had shown how newly created neurons in adults rely on signals from distant brain regions to regulate their maturation and survival.

The new neurons do this before the start of communication with the existing cells in their immediate neighborhood — a key finding that had important implications for using adult neural stem cells to replace brain cells lost by trauma or neurodegeneration.

Those earlier findings appeared in The Journal of Neuroscience. [C2]

All image adapted from originals courtesy of Sonya Giridhar
Both approaches are important, but the scientists wanted to find out how the brain decided which method to use to process a sensory input. They looked at mitral cell neurons in the brain's olfactory bulb — the part of the brain that sorts out smells and a common model for studying global information processing.

What happens before new neuron growth?

Using slice electrophysiology and computer simulations, the researchers found that the brain had a clever strategy for ensuring that the neurons' message was being heard. Over the short time scale of a few milliseconds, the brain engaged its inhibitory circuitry to make the neurons fire in synchrony. This simultaneous, correlated firing creates a loud, but simple, signal. The effect was much like a crowd at a sporting event chanting, "Let's go team!"

Over short time intervals, individual neurons produced the same short message, increasing the effectiveness with which activity was transmitted to other brain areas. The researchers say that in both human and neuronal communication alike, this collective communication works well for simple messages, but not for longer or more complex messages that contain more intricate information.

The neurons studied used longer timescales (around one second) to convey these more complex concepts. Over longer time intervals, the inhibitory circuitry generated a form of competition between neurons, so that the more strongly activated neurons silenced the activity of weakly activated neurons, enhancing the differences in their firing rates and making their activity less correlated. Each neuron was able to communicate a different piece of information about the stimulus without being drowned out by the chatter of competing neurons.

It would be like being in a group where each person spoke in turn. The room would be much quieter than a sports arena and the immediate audience would be able to listen and learn much more complex information.

Researchers believe that the findings can be applied beyond the olfactory system to other neural systems, and perhaps even be used in other biological systems.

What happens after new neuron growth?

Certain important synaptic connections--the circuitry that allows the brain cells to talk to each other — do not appear until 21 days after the birth of the new cells, according to Charles Greer, professor of neurosurgery and neurobiology, and senior author of an earlier study on the effects on communication of new neuron growth. [C2]

In the meantime, other areas of the brain provide information to the new cells, preventing them from disturbing ongoing functions until the cells are mature.

It had been established in even earlier studies that several regions of the adult brain continue to generate new neurons, which are then integrated into existing brain circuitry. However the mechanisms that allowed this to happen were not known.

To answer this question, Greer and Mary Whitman, an M.D./Ph.D. candidate at Yale, studied how new neurons are integrated into the olfactory bulb, which helps discriminate between odors, among other functions.

They found that new neurons continue to mature for six to eight weeks after they are first generated and that the new neurons receive input from higher brain regions for up to 10 days before they can make any outputs. The other brain regions then continue to provide information to the new neurons as they integrate into existing networks.

The progress of neuron research

Regarding the earlier research [C2], the discovery of a previously unrecognized mechanism was significant, Charles Greer said at the time, because "if we want to use stem cells to replace neurons lost to injury or disease, we must ensure that they do not fire inappropriately, which could cause seizures or cognitive dysfunction."

The accumulation of these kinds research results over the years has proven significant in understanding how the brain constantly renews itself, guided by the developmental body plan to ensure consistency and renewal.

Remarking on the current research, [C1] Nathan Urban says "Across biology, from genetics to ecology, systems must simultaneously complete multiple functions. The solution we found in neuroscience can be applied to other systems to try to understand how they manage competing demands." Urban is Professor of Life Sciences and head of the Department of Biological Sciences at CMU.

FundingThe [C1] study was funded by the National Institute on Deafness and Other Communications Disorders (NIDCD), the National Institutes of Health (NIH) and the National Science Foundation (NSF).
ParticipationCo-authors of the [C1] study include Brent Doiron, assistant professor of mathematics at the University of Pittsburgh, and Sonya Giridhar, a doctoral student in the Center for Neuroscience at Pitt. Both are members of the Center for the Neural Basis of Cognition.
Citation[C1] Timescale-dependent shaping of correlation by olfactory bulb lateral inhibition. Sonya Giridhara, Brent Doirona, and Nathaniel N. Urban. Proceedings of the National Academy of Sciences 2011; ePub ahead of print. doi:10.1073/pnas.1015165108

Abstract

Neurons respond to sensory stimuli by altering the rate and temporal pattern of action potentials. These spike trains both encode and propagate information that guides behavior. Local inhibitory networks can affect the information encoded and propagated by neurons by altering correlations between different spike trains. Correlations introduce redundancy that can reduce encoding but also facilitate propagation of activity to downstream targets. Given this trade-off, how can networks maximize both encoding and propagation efficacy? Here, we examine this problem by measuring the effects of olfactory bulb inhibition on the pairwise statistics of mitral cell spiking. We evoked spiking activity in the olfactory bulb in vitro and measured how lateral inhibition shapes correlations across timescales. We show that inhibitory circuits simultaneously increase fast correlation (i.e., synchrony increases) and decrease slow correlation (i.e., firing rates become less similar). Further, we use computational models to show the benefits of fast correlation/slow decorrelation in the context of odor coding. Olfactory bulb inhibition enhances population-level discrimination of similar inputs, while improving propagation of mitral cell activity to cortex. Our findings represent a targeted strategy by which a network can optimize the correlation structure of its output in a dynamic, activity-dependent manner. This trade-off is not specific to the olfactory system, but rather our work highlights mechanisms by which neurons can simultaneously accomplish multiple, and sometimes competing, aspects of sensory processing.



[C2] Synaptic Integration of Adult-Generated Olfactory Bulb Granule Cells: Basal Axodendritic Centrifugal Input Precedes Apical Dendrodendritic Local Circuits. Mary C. Whitman and Charles A. Greer. The Journal of Neuroscience 27(37): 9951-9961. doi:10.1523/JNEUROSCI.1633-07.2007
Download PDF
Abstract

The adult mammalian olfactory bulb (OB) receives a continuing influx of new interneurons. Neuroblasts from the subventricular zone (SVZ) migrate into the OB and differentiate into granule cells and periglomerular cells that are presumed to integrate into the synaptic circuits of the OB. We have used retroviral infection into the SVZ of mice to label adult-generated granule cells and follow their differentiation and integration into OB circuitry. Using synaptic markers and electron microscopy, we show new granule cells integrating into the reciprocal circuitry of the external plexiform layer (EPL), beginning at 21 d postinfection (dpi). We further show that synapses are formed earlier, beginning at 10 dpi, on the somata and basal dendrites of new cells in the granule cell layer (GCL), before dendritic elaboration in the EPL. In the EPL, elaborate dendritic arbors with spines are first evident at 14 dpi. The density of spines increases from 14 to 28 dpi, and then decreases by 56 dpi. Despite the initial appearance of dendritic spines at 14 dpi in the EPL, no expression of presynaptic or postsynaptic markers is seen until 21 dpi. These data suggest that adult-generated granule cells are first innervated by centrifugal or mitral/tufted cell axon collaterals in the GCL and that these inputs may contribute to their differentiation, maturation, and synaptic integration into the dendrodendritic local circuits found in the EPL.

Keywords: neurogenesis, synaptogenesis, dendrite, spine, cholinergic, rostral migratory stream.

TS-Si News ServiceThe TS-Si News Service is a collaborative effort by TS-Si.org editors, contributors, and corresponding institutions. The sources can include the cited individuals and organizations, as well as TS-Si.org staff contributions. Articles and news reports do not necessarily convey official positions of TS-Si, its partners, or affiliates.

We welcome your comments. Use the form below to leave a public comment or send private correspondence via the TS-Si Contact Page. We will not divulge any personal details or place you on a mailing list without your permission.


TS-Si is dedicated to the acceptance, medical treatment, and legal protection of individuals correcting the misalignment of their brains and their anatomical sex, while supporting their transition into society as hormonally reconstituted and surgically corrected citizens.

Quote this article on your site

To create link towards this article on your website,
copy and paste the text below in your page.




Preview :


Comments (0)

Write comment

Last Updated on Sunday, 03 April 2011 14:41
 
FeedFeed2CommentsDeliciousDiggFacebookTwitter