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DNA Blueprints Guide The Construction Of Specific Human Structures
Chad Mirkin discusses using DNA to build a three-dimensional structure out of gold, likening the process to building a house. Starting with basic materials such as bricks, wood, siding, stone and shingles, a construction team can build many different types of houses out of the same building blocks.
The article includes an audio recording of the full interview. Photo courtesy of the UCSD School of Medicine.
| Neuroscience Memory Mission Explores New Territory |
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| Science - Neuroscience | ||||
| TS-Si News Service | ||||
| Tuesday, 02 December 2008 09:00 | ||||
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Richards' research team has returned to basics, looking at how the brain forms during embryonic and foetal development. She and her colleagues have identified a gene that regulates the development of glial cells in the hippocampus. Their research shows that the hippocampus contains different populations of glial cells that are essential for the structural integrity of the hippocampus.
According to QBI's Associate Professor Linda Richards, knowledge of the early development of the hippocampus remains surprisingly scant, despite the crucial role performed by this region throughout life. [N1,2] "Glial cells are an important part of the building blocks of the brain," Dr Richards said.
"They provide an essential scaffold for the migration of neurons in the developing brain. It is vital we understand how glial cells provide this structural scaffold because if the hippocampus is not formed correctly it cannot perform all the functions required of it in the developing and adult brain," she said.
"The hippocampus plays an integral role in spatial navigation, learning and memory, and is a major site for adult neurogenesis."
Neurogenesis literally refers to the birth of neurons, the process by which neurons are created. It is most active during pre-natal development and continues beyond the pre-natal period to populate the growing brain.
Adult neurogenesis has recently been observed in mammals, including humans.
Previous investigations had suggested that the new cells may be glial cells, known as the "glue" of the nervous system. Glia are estimated to outnumber neurons in the human brain by about 10 to 1.
Mice lacking the gene that regulates glial cell differentiation exhibit major developmental irregularities, including catastrophic structural deformities of the hippocampus.
Equipped with this knowledge, researchers studying the hippocampus now have a better understanding of the genes that help control the development of this vital brain region.
Fundamental scientific knowledge of this kind is an essential step in understanding brain function and repair.
Notes[N1] The term hippocampus is derived from the Greek words hippos (horse) and campus (sea monster). The brain region known as the hippocampus has the characteristic shape of a sea-horse's tail.
[N2] The hippocampus is a region of the brain crucial to memory formation and the lifelong production and integration of new nerve cells. Corresponding AuthorLinda Richards, PhD, is an associate professor and the Head of Cortical Development and Axon Guidance at QBI. Dr. Richards' laboratory investigates how the brain becomes wired up during development, focusing on the development of the cerebral cortex, a region of the brain where all higher order cognition is processed.
CitationSpecific Glial Populations Regulate Hippocampal Morphogenesis. Guy Barry, Michael Piper, Charlotta Lindwall, Randal Moldrich, Sharon Mason, Erica Little, Anindita Sarkar, Shubha Tole, Richard M. Gronostajski, and Linda J. Richards1. Journal of Neuroscience 28(47): 12328 doi: 10.1523 / JNEUROSCI.4000-08.2008.
Abstract The hippocampus plays an integral role in spatial navigation, learning and memory, and is a major site for adult neurogenesis. Critical to these functions is the proper organization of the hippocampus during development. Radial glia are known to regulate hippocampal formation, but their precise function in this process is yet to be defined. We find that in Nuclear Factor I b (Nfib)-deficient mice, a subpopulation of glia from the ammonic neuroepithelium of the hippocampus fail to develop. This results in severe morphological defects, including a failure of the hippocampal fissure, and subsequently the dentate gyrus, to form. As in wild-type mice, immature nestin-positive glia, which encompass all types of radial glia, populate the hippocampus in Nfib-deficient mice at embryonic day 15. However, these fail to mature into GLAST- and GFAP-positive glia, and the supragranular glial bundle is absent. In contrast, the fimbrial glial bundle forms, but alone is insufficient for proper hippocampal morphogenesis. Dentate granule neurons are present in the mutant hippocampus but their migration is aberrant, likely resulting from the lack of the complete radial glial scaffold usually provided by both glial bundles. These data demonstrate a role for Nfib in hippocampal fissure and dentate gyrus formation, and that distinct glial bundles are critical for correct hippocampal morphogenesis.
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| Last Updated on Monday, 01 December 2008 21:42 |








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The TS-Si News Service is a collaboration of TS-Si staff, contributors, and corresponding institutions. Contents do not necessarily convey official positions of TS-Si, its partners, or affiliates