Stem cell discoveries pace growing understanding of human brain's uniqueness
(Medical Xpress) -- Scientists are making great strides in figuring out how the human brain with its expansive cerebral cortex and corresponding capacity for higher thinking became one of natures greatest wonders. Insights about how the brain develops are leading to novel ideas about the causes of a range of brain disorders, and are raising hopes for the regeneration of tissue that is lost in diseases such as Alzheimers. At the center of this scientific ferment are new stem cell discoveries by researchers at UCSF.
Stem Cells Drive Expansion of Brains Cortex
Like the phyllo dough crust in baklava and certain other Greek and Middle Eastern delicacies, the reptilian and mammalian cortices are made from thin layers. In reptiles, the cortex has three layers; in mammals, it has six. The entire cortex is about two millimeters thick.
While human brains have the same six cortical layers as brains from less well-equipped mammals, these sheets of cortical brain matter extend outward much farther in humans. Furthermore, in Homo sapiens and other primates, the cortex folds many times. The folding allows more neural circuitry to fit into the skull and gives the human brain its unique architecture and cauliflower-like appearance.
The human brain has an enormously expanded surface area in the cerebral cortex, says Arnold Kriegstein, MD, PhD, director of the Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research at UCSF. Like the abundance of chips and transistors in a supercharged computer, all those added neurons form more circuits, allowing for more computation and more sophisticated kinds of processing. For us, the payoff is conscious thought, reasoning and language and the wherewithal to build rich civilizations that span the globe.
Last year, Kriegsteins laboratory team reported the identification of a long-elusive stem cell that we may have to thank for our success as a species. The stem cell appears to be responsible for the explosive growth of neurons that occurs in a part of the fetal primate brain known as the outer subventricular zone (OSVZ).
If the neurons in the brain were like people in a metropolis, the fetal brains mid-gestational growth spurt in the OSVZ would be like the suburban population boom on the outskirts of cities in the late 1900s.
Each time the OSVZ neural stem cell divides, it regenerates itself and also spins off an intermediary cell. These intermediary cells, in turn, divide many times to produce specialized neurons. Each stem cell sends a branch upward through the layers of cortex, and this extension acts like a guide wire for newborn neurons traveling through the cortical layers.
There is a whole region thats found in the human brain, but not in the rodent, where cells are born and delivered to the developing layers of the cortex, Kriegstein says. The newly described stem cells are responsible both for making the nerve cells and for guiding them to their proper locations in the cortex, where they form cell columns.
As in all regions of the cortex, the neurons in these vertical columns form electrical circuits, and myriad columns are aligned horizontally throughout the plane of the cortex. The recently discovered OSVZ stem cell and its progeny appear to drive growth outward from the edges of this horizontal plane, Kriegstein says.
Evolution from Mouse to Human
Although the OSVZ region is absent in the mouse, Kriegsteins lab team nonetheless went looking in the mouse brain for a stem cell similar to the OSVZ stem cell. They found it, but only in small numbers. Furthermore, in the mouse, these stem cells do not spin off the intermediate progenitors that powerfully amplify the growth of new neurons in the human brain.
Still, this latest rodent discovery more closely links mice and humans, and there is a possibility that the mouse may become a more valuable tool for studying human brain disorders as a result, according to Kriegstein. Kriegsteins lab team describes its latest mouse studies in the April 10 online edition of Nature Neuroscience.
This tells us that this type of stem cell developed more than 100 million years ago, Kriegstein says. That means the process of cortical evolution was more gradual than many had thought. This is not a feature that suddenly arrived in the primate. It developed over a very long period of time through successive alterations and changes, and it eventually led to what we have in the human.
In both humans and mice, scientists had previously identified brain stem cells that generate neurons from the edges of the ventricles fluid-filled spaces at the center of the brain and from a layer, called the subventricular region, just above the ventricles. These earlier-arising stem cells produce fewer neurons in comparison with the human OSVZ stem cells and their daughter cells. Even if their inherent growth potential were not already limited, their expansion would be limited by the size of the ventricles, Kriegstein says.
As the name implies, the outer subventricular zone is farther away from the ventricles. The intermediate progenitors spun off by the OSVZ stem cells are free to propagate neurons with little constraint, Kriegstein says. The folding cortex can expand farther and still fit within the skull.
Stem Cell Movement Before Cell Division Is Linked to Brain Development
Using real-time imaging of brain tissue under the microscope and fluorescently labeled molecular markers, Kriegsteins lab team discovered peculiar movements in stem cells shortly before they underwent cell division. The movements never seen before are distinctive and are different in the various stem cell types, Kriegstein says. Defects in the machinery controlling these movements might play a role in different brain malformations, he believes.
Its only because we were making movies that we were able to see these movements, he says. Were not sure why the cells are doing this, but were very interested in finding out.
In each case, the stem cells nucleus moves through the cells long, extended arm before dividing, but in the different types of stem cells, the nucleus moves in different directions. The movements affect the positioning of daughter cells after the stem cell divides.
Key to these movements are structures found in every dividing cell namely, a pair of centrosomes. Centrosomes are poles that form on opposite sides of the cells nucleus prior to cell division. Fibrous spindles emanate from these poles and are used to pull replicated chromosomes apart, so that the chromosomes and the entire DNA they contain can be divided between daughter cells.
Mutations that affect the performance of centrosomes already have been associated with inborn disorders. One such disorder is lissencephaly, in which the cortex fails to fold up into its cauliflower shape. Another is microcephaly, in which the brain appears more or less normal, but may be as little as half the size of a healthy brain.
One possibility, Kriegstein says, is that if the OSVZ stem cells fail to pump out the number of new neurons needed for the cortex to grow outward and fold properly, lissencephaly may be the result. On the other hand, he adds, if stem cells in the ventricular region generate too few neurons, then microcephaly may be the result.
Mouse Models May Prove More Useful Than Expected
Schizophrenia and autism are considered to be diseases of abnormal brain development, Kriegstein notes. Scientists had considered the mouse brain too simple to help them understand the origins of these human afflictions. But now the Kriegstein lab teams discovery of a new type of stem cell shared by the two mammals raises hope that the mouse can provide at least some clues about normal cellular behaviors in developmental pathways that may go awry in these disorders.
The continued exploration of different stem cell types and the identification of the types of neurons that are their descendants are crucial to obtaining a better understanding of a range of neurological disorders that strike specific types of neurons or brain regions while sparing others, Kriegstein says. Among the most common of these disorders are Alzheimers disease and Parkinsons disease.
Similar studies are required to develop the capability to reliably grow the specific types of neurons needed to regenerate tissue that is damaged as a result of these diseases, according to Kriegstein.
Neurons During Development A Cellular Family Tree
Real-time imaging already has been a valuable tool in studying cell lineages during development, Kriegstein says.
By simply looking at these cells in fixed tissue, you can get a sense of the diversity of cells you can find, but it does not tell you where they came from or how they relate to each other, he says. But by watching one cell divide, and then by watching the daughter cells migrate and divide, you begin to see the relationships between different cell types. One type is derived from another. Thats information you really couldnt get any other way.
We are looking for active genes that are unique to each type of neuron-producing stem cell or progenitor cell, he adds. Were sure they exist, but we dont know what they are yet. When we find them, we will be able to use them to sort cells and, ultimately, to make huge numbers of specific types of neurons in the laboratory.
Then we can really go to town with studies of diseases that affect specific cell types in the brain.
A hallmark of mammalian brain evolution is cortical expansion, which reflects an increase in the number of cortical neurons established by the progenitor cell subtypes present and the number of their neurogenic divisions. Recent studies have revealed a new class of radial glialike (oRG) progenitor cells in the human brain, which reside in the outer subventricular zone. Expansion of the subventricular zone and appearance of oRG cells may have been essential evolutionary steps leading from lissencephalic to gyrencephalic neocortex. Here we show that oRG-like progenitor cells are present in the mouse embryonic neocortex. They arise from asymmetric divisions of radial glia and undergo self-renewing asymmetric divisions to generate neurons. Moreover, mouse oRG cells undergo mitotic somal translocation whereby centrosome movement into the basal process during interphase precedes nuclear translocation. Our finding of oRG cells in the developing rodent brain fills a gap in our understanding of neocortical expansion.