Defining the Brain Mosaic in Fruit Flies and Humans

Summary: A new study reveals the same calcium signaling mechanism is required to generate specific classes of neurons in the brain.

Source: National Center for Biological Sciences.

Similar to a mosaic floor where different patterned tiles come together to make a composite and holistic image, our brains too consist of billions of unique neurons that finally connect together and generate coordinated brain activity. Unlike the mosaic floor, however, which is static, our brains are dynamic and activity in the brain changes based on environmental cues. So, what makes up the mosaic of our brain? Or, in other words, how are individual neurons different from each other? The presence or absence of special types of proteins on individual neurons makes them unique and the complete range of such proteins on a neuron defines its characteristic ability to respond differentially to particular internal or external stimuli. When individual neurons lose their characteristic protein combination it can lead to faulty brain activity followed by neurodegeneration diseases and psychiatric disorders. And so, identifying mechanisms that define which protein is present on which neurons, are of utmost importance.

Our recent work, published recently in the international journal eNeuro, has shown that across species ranging from fruit flies to humans, neurons in the newly-formed brain utilize a novel form of calcium signaling called store-operated calcium entry or SOCE, to express the correct range of proteins. During SOCE neurons bring calcium from outside the cell to refill depleted cellular calcium stores that happens during the neuronal response to a range of signals (such as hormones, neuropeptides, and even neurotransmitters). The function of SOCE in neurons has been difficult to understand primarily because neurons have several alternate mechanisms of calcium entry. We have used targeted genetic approaches to study how SOCE affects neuronal function in Drosophila neurons and more recently in neuronal precursor cells derived from human stem cells.

The fruit fly like many other insects goes through a crawling larval stage that becomes a sessile pupa in which the larval brain is re-modeled for life as a fly. Inside the apparently dormant pupa, however, neurons that are being re-modeled are busy making the right connections with other neurons – a process called neural circuit development. When proteins required for calcium signaling were removed specifically from neurons of the flight circuit, flies that emerged from pupae were unable to fly for long. By comparing brains from such poorly flying flies with normal flies it became clear that specific proteins that help neurons talk to each other were present at much lower levels when calcium signaling is impaired in the developing flight circuit of a fruit fly pupa.

Our earlier work showed that genes encoding these proteins were themselves expressed at lower levels when calcium signaling was impaired. The importance of these genes and the proteins encoded by them, for normal brain activity was evident when putting some of them back in a fruit fly with impaired calcium signaling allowed for much better flight. In these “rescued” flies the ability of flight neurons to talk to each other–by a process called neurotransmission–also improved.

A majority of cellular and molecular processes are conserved in organisms separated from each other across large evolutionary timescales. Thus, studies from the fruit fly have helped understand aspects of human development, behavior, and disease. Because direct experiments that test if gene expression in neurons of the human brain requires calcium signaling are not possible, we chose instead to test this idea in human neural precursor cells derived from human stem cells. Indeed, here too loss of a particular class of calcium signaling lead to altered gene and protein expression. As shown in our recently published article in Frontiers in Molecular Neuroscience, the neural precursor cells became more neuron-like at an earlier stage suggesting that calcium signaling during development helps in expression of proteins required to maintain neural precursor cells in a state where they can divide and make more cells like themselves. This finding is potentially important for understanding disease syndromes that affect normal growth of the human brain.

A majority of cellular and molecular processes are conserved in organisms separated from each other across large evolutionary timescales. image is in the public domain.

Our findings from the fruit fly and human neural precursor cells show that the same calcium signaling mechanism is required for generating specific classes of neurons in the brain. In the fruit fly we know that loss of such signaling affects their ability to fly normally. In the human brain it is potentially implicated in growth at earlier stages of brain formation. Does the loss of such calcium signaling in adult human neurons also change their function and affect human health? Work from other labs suggests that this might be the case. For example, in the human neurodegenerative disorder spinocerebellar ataxia 15 calcium signaling is reduced due to inherited mutations. Is this due to changes in gene expression in the affected neurons over time? The answer to this question will have to wait for the next set of experiments.

About this neuroscience research article

Funding: Canadian Institutes of Health Research, Canada Research Chair Award, Sandra and Alain Bouchard Intellectual Disabilities Platform funded this study.

Source: Gaiti Hasan – National Center for Biological Sciences
Publisher: Organized by
Image Source: image is in the public domain.
Original Research: Open access research for “Stable STIM1 Knockdown in Self-Renewing Human Neural Precursors Promotes Premature Neural Differentiation” by Renjitha Gopurappilly, Bipan Kumar Deb, Pragnya Chakraborty and Gaiti Hasan in Frontiers in Molecular Neuroscience. Published June 11 2018.

Cite This Article

[cbtabs][cbtab title=”MLA”]National Center for Biological Sciences “Defining the Brain Mosaic in Fruit Flies and Humans.” NeuroscienceNews. NeuroscienceNews, 26 June 2018.
<>.[/cbtab][cbtab title=”APA”]National Center for Biological Sciences (2018, June 26). Defining the Brain Mosaic in Fruit Flies and Humans. NeuroscienceNews. Retrieved June 26, 2018 from[/cbtab][cbtab title=”Chicago”]National Center for Biological Sciences “Defining the Brain Mosaic in Fruit Flies and Humans.” (accessed June 26, 2018).[/cbtab][/cbtabs]


Stable STIM1 Knockdown in Self-Renewing Human Neural Precursors Promotes Premature Neural Differentiation

Ca2+ signaling plays a significant role in the development of the vertebrate nervous system where it regulates neurite growth as well as synapse and neurotransmitter specification. Elucidating the role of Ca2+ signaling in mammalian neuronal development has been largely restricted to either small animal models or primary cultures. Here we derived human neural precursor cells (NPCs) from human embryonic stem cells to understand the functional significance of a less understood arm of calcium signaling, Store-operated Ca2+ entry or SOCE, in neuronal development. Human NPCs exhibited robust SOCE, which was significantly attenuated by expression of a stable shRNA-miR targeted toward the SOCE molecule, STIM1. Along with the plasma membrane channel Orai, STIM is an essential component of SOCE in many cell types, where it regulates gene expression. Therefore, we measured global gene expression in human NPCs with and without STIM1 knockdown. Interestingly, pathways down-regulated through STIM1 knockdown were related to cell proliferation and DNA replication processes, whereas post-synaptic signaling was identified as an up-regulated process. To understand the functional significance of these gene expression changes we measured the self-renewal capacity of NPCs with STIM1 knockdown. The STIM1 knockdown NPCs demonstrated significantly reduced neurosphere size and number as well as precocious spontaneous differentiation toward the neuronal lineage, as compared to control cells. These findings demonstrate that STIM1 mediated SOCE in human NPCs regulates gene expression changes, that in vivo are likely to physiologically modulate the self-renewal and differentiation of NPCs.

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