BMP signalling facilitates transit amplification in the developing chick and human cerebellum

Curation statements for this article:
  • Curated by eLife

    eLife logo

    eLife assessment

    This is an important study that investigates BMP signaling mechanisms in the developing chick cerebellum to better understand germinal layer formation, cellular amplification and neuronal differentiation. The data from human tissue is compelling and lends support to the possible links of these processes to medulloblastoma, although these specific statements could be toned down and presented only as part of the discussion. Overall, this is a solid piece of work with beautifully presented findings.

This article has been Reviewed by the following groups

Read the full article See related articles

Abstract

The external granule layer (EGL) is a transient proliferative layer that gives rise to cerebellar granule cell neurons. Extensive EGL proliferation characterises the foliated structure of amniote cerebella, but the factors that regulate EGL formation, amplification within it, and differentiation from it, are incompletely understood. Here, we characterise bone morphogenic protein (BMP) signalling during cerebellar development in chick and human and show that while in chick BMP signalling correlates with external granule layer formation, in humans BMP signalling is maintained throughout the external granule layer after the onset of foliation. We also show via Immunohistochemical labelling of phosphorylated Smad1/5/9, that the spatiotemporal activity of BMP signalling is conserved between chick and human. Using in ovo electroporation in chick, we demonstrate that BMP signalling is necessary for subpial migration of granule cell precursors and hence the formation of the external granule layer (EGL) prior to transit amplification. However, altering BMP signalling does not block the formation of mature granule neurons but significantly disrupts that pattern of morphological transitions that accompany transit amplification. Our results elucidate two key, temporally distinct roles for BMP signalling in vivo in organising first the assembly of the EGL from the rhombic lip and subsequently the tempo of granule neuron production within the EGL.Improper development of cerebellar granule neurons can manifest in a plethora of neurodevelopmental disorders, including but not limited to medulloblastoma and autism. Medulloblastoma can be a consequence of uncontrolled proliferation of granule cell progenitors, with BMP overexpression being a potential therapeutic avenue to inhibit this proliferation. Many studies have sought to understand the role of developmental signalling pathways in granule cell neurogenesis, using genetic manipulation in transgenic mice. To complement these insights, we have used comparative assessment of BMP signalling during development in chick and human embryos and in vivo manipulation of the chick to understand and segregate the spatiotemporal roles of BMP signalling, yielding important insights on evolution and in consideration of future therapeutic avenues that target BMP signalling.

Article activity feed

  1. eLife assessment

    This is an important study that investigates BMP signaling mechanisms in the developing chick cerebellum to better understand germinal layer formation, cellular amplification and neuronal differentiation. The data from human tissue is compelling and lends support to the possible links of these processes to medulloblastoma, although these specific statements could be toned down and presented only as part of the discussion. Overall, this is a solid piece of work with beautifully presented findings.

  2. Reviewer #1 (Public Review):

    Summary:
    Rook et al examined the role of BMP signaling in cerebellum development, using chick as a model alongside human tissue samples. They first examined p-SMADs and found differences between the species, with human samples retaining high p-SMAD after foliation, while in chick, BMP signaling appears to decrease following foliation. To understand the role of BMP during early development, they then used early chick embryos to modulate BMP, using either a constitutively active BMP regulator to increase BMP signaling or overexpressing the negative intracellular BMP regulator to decrease BMP signaling. After validating the constructs in ovo, the authors then examined GNP morphology and migration. They then determined whether the effects were cell autonomous.

    Strengths:
    The experiments were well-designed and well-controlled. The figures were extremely clear and convincing, and the accompanying drawings help orient the reader to easily understand the experimental set up. These studies also help clarify the role of BMP at different stages of cerebellum development, suggesting early BMP signaling is required for dorsalization, not rhombic lip induction, and that later BMP signaling is needed to regulate the timing of migration and maturation of granule neurons.

    Weaknesses:
    Given the species-specific differences in pSmad localization and abundance in human and chick cerebellum, caution is warranted when making the link to the treatment of human medulloblastoma through modulation BMP signaling. While these studies certainly hint that BMP modulation may affect tumor growth, this was not explicitly tested here. Future studies are required to generalize the functional role of BMP signaling in normal cerebellum development to malignant growth.

  3. Reviewer #2 (Public Review):

    Summary:
    This is a fundamental and elegant study showing the role of BMP signaling in cerebellar development. This is an important question because there are multiple diseases, including aggressive childhood cancers, which involve granule cell precursors. Thus understanding of the factors that govern the formation of the granule cell layer is important both from a basic science and a disease perspective.

    Overall, the manuscript is clear and well-written. The figures are extremely clear, wonderfully informative, and overall quite beautiful.

    Figures 1-3 show the experimental design and report how BMP activity is altered over development in both the chick and the human developing cerebellum. Both data are very impressive and convincing.

    They then go on to modulate BMP activity in the developing chick, using a complex electroporation paradigm that allows them to label cells with GFP as well as with cell-specific reporters of BMP activity levels. They bidirectionally modulate BMP levels and then can look at both cell-specific and non-specific alterations in the formation of the external and internal granule cell layer, across different developmental timepoints. These are really elegant and rigorous experiments, as they look at both sagittal and transverse sections to collect this data. This makes the data extremely compelling. With these rigorous techniques, they show that BMP signaling serves more than one function across development: it is involved in the initial tangential migration from the rhombic lip, but at a later time, both up- and down-regulation of BMP activity reduces the density of amplifying cells in the external granule cell layer.

    Strengths:
    Overall, I think the paper is interesting and important and the data is strong. The use of both chick and human tissue strengthens the findings. They are extremely rigorous, analyzing data from multiple planes at multiple ages, which also really strengthens their findings. The dual electroporation approach is extremely elegant, providing beautiful visual representations of their findings.

    Weaknesses:
    I find no significant weaknesses.