Summary: A new study reveals subplate cells may not simply disappear, they may, instead, be migrating to different levels of the cortex. In essence, subplate cells may become part of the cerebral cortex.
Source: Rockefeller University.
The disappearance of an entire brain region should be cause for concern. Yet, for decades scientists have calmly maintained that one brain area, the subplate, simply vanishes during the course of human development. Recently, however, research has revealed genetic similarities between cells in the subplate and neurons implicated in autism–leading a team of Rockefeller scientists to wonder: what if subplate cells don’t actually vanish at all?
In a new paper, which appears in Cell Stem Cell, Ali H. Brivanlou, the Robert and Harriet Heilbrunn Professor, and postdoctoral associate Zeeshan Ozair demonstrate that subplate neurons survive, and in fact become part of the adult cerebral cortex, a brain area involved in complex cognitive functions. The team outlines a connection between subplate neurons and certain brain disorders, and further identifies a strategy for treating such disorders via innovative stem cell techniques.
A happier fate
In the developing brain, the subplate sits below the cortical plate, a precursor to the cortex. During some stages of development, the subplate is the largest layer of the brain–making its ultimate disappearance all the more confounding.
“The understanding about the subplate was that it expands and then the cells of the subplate just die out. But we hypothesized: What if these subplate cells are not dying? What if they’re just moving to a different level of the cortex–becoming part of the cortex?” says Brivanlou.
He and his colleagues found ample support for this idea. In samples of brain tissue from various developmental stages, they detected PRDM8, a protein expressed in migrating neurons that helps cells move into the cortical plate. They also detected PRDM8 in subplate-like neurons that they generated from stem cells; and experiments showed that these laboratory-grown subplate neurons wandered away from their original location. All of these findings pointed not to cell death, but to cell movement.
Far from a site of demise, the subplate seems to nurture the development of functional and diverse cells. Ozair and Brivanlou observed that subplate neurons mature into various types of deep projection neurons–cells found in the deepest layers of the cortex.
The subplate’s subplot
In other experiments, the researchers modulated the levels of WNT signaling, a pathway known to guide many developmental processes. They found that the level of WNT signaling determined the fate of subplate neurons: low levels yielded projection neurons that extend within the cortex, and high levels yielded neurons that project to other brain areas.
These findings have significant implications for understanding brain disorders. Projection neuron abnormalities have been linked to several neurodevelopmental conditions, including autism; and Brivanlou and Ozair’s research suggests that these abnormalities manifest very early in development. “A lot of the genes associated with autism are first expressed in the subplate,” says Ozair. “And if subplate neurons don’t die but instead become part of the cortex, they will carry those mutations with them.”
In addition to shedding light on the early stages of brain disorders, the research presents new hope for preventing or treating such disorders through stem-cell therapy. For example, the scientists hope that their findings will one day make it possible to treat neurodegenerative disease using techniques to generate scarce neuronal subtypes from subplate-like stem cells.
“The deep layers of the cortex are involved in many diseases: Alzheimer’s, Lou Gehrig’s, and Huntington’s disease all kill off specific types of deep-projection neurons,” says Ozair. “When we think about cellular-replacement therapy, we need to think about how these cells are made in the first place.”
Brivanlou adds: “This research shows us how to generate these neurons directly, because we know the signaling mechanism that is necessary for their fate to be unveiled.”
Funding: This work was supported by NYSTEM, Tri-Institutional Stem Cell Initiative.
Source: Greg Williams – Rockefeller University
Publisher: Organized by NeuroscienceNews.com.
Image Source: NeuroscienceNews.com image is credited to Laboratory of Stem Cell Biology and Molecular Embryology at The Rockefeller University.
Original Research: Abstract for “hPSC Modeling Reveals that Fate Selection of Cortical Deep Projection Neurons Occurs in the Subplate” by M. Zeeshan Ozair, Christoph Kirst, Bastiaan L. van den Berg, Albert Ruzo, Tiago Rito, and Ali H. Brivanlou in Cell Stem Cell. Published June 21 2018.
[cbtabs][cbtab title=”MLA”]Rockefeller University “Researchers Solve the Case of the Missing Subplate.” NeuroscienceNews. NeuroscienceNews, 23 June 2018.
<https://neurosciencenews.com/subplate-mystery-9428/>.[/cbtab][cbtab title=”APA”]Rockefeller University (2018, June 23). Researchers Solve the Case of the Missing Subplate. NeuroscienceNews. Retrieved June 23, 2018 from https://neurosciencenews.com/subplate-mystery-9428/[/cbtab][cbtab title=”Chicago”]Rockefeller University “Researchers Solve the Case of the Missing Subplate.” https://neurosciencenews.com/subplate-mystery-9428/ (accessed June 23, 2018).[/cbtab][/cbtabs]
hPSC Modeling Reveals that Fate Selection of Cortical Deep Projection Neurons Occurs in the Subplate
Cortical deep projection neurons (DPNs) are implicated in neurodevelopmental disorders. Although recent findings emphasize post-mitotic programs in projection neuron fate selection, the establishment of primate DPN identity during layer formation is not well understood. The subplate lies underneath the developing cortex and is a post-mitotic compartment that is transiently and disproportionately enlarged in primates in the second trimester. The evolutionary significance of subplate expansion, the molecular identity of its neurons, and its contribution to primate corticogenesis remain open questions. By modeling subplate formation with human pluripotent stem cells (hPSCs), we show that all classes of cortical DPNs can be specified from subplate neurons (SPNs). Post-mitotic WNT signaling regulates DPN class selection, and DPNs in the caudal fetal cortex appear to exclusively derive from SPNs. Our findings indicate that SPNs have evolved in primates as an important source of DPNs that contribute to cortical lamination prior to their known role in circuit formation.