The video outlines a detailed protocol for culturing human induced pluripotent stem cells (iPSCs) into cerebral organoids. It includes steps for cell detachment, creating embryoid bodies, embedding them in a basement membrane matrix, and culturing organoids in a specific environment for optimal development and maintenance.

generation of cerebral organoids from primate-induced pluripotent stem cells (ipscs)

Genetic Modification of Primate Cerebral Organoids

Investigating the (patho)physiological development and evolution of the cerebral cortex is a formidable task that is hampered by the lack of suitable model systems. Previously, such studies were confined to two-dimensional cell culture models (such as primary neural progenitor or neuronal cell cultures) and evolutionarily distant animal models (such as rodents)1,2. While these models are useful for addressing certain questions, they are limited in modeling the complexity, cell type composition, cellular architecture, and gene expression patterns of the developing human neocortex in healthy and diseased states. These limitations lead, for example, to the poor translatability of mouse models of human diseases to the human situation, as described for certain cases of microcephaly (e.g., Zhang et al.3). Recently, transgenic non-human primates, which are an evolutionarily, functionally, and morphologically closer model of human neocortex development, have come into focus4,5,6,7,8 as they overcome many limitations of cell culture- and rodent-based models. However, the use of non-human primates in research is not only highly expensive and time-consuming but also raises ethical concerns. More recently, the development of brain organoid technology9,10 has emerged as a promising alternative that solves many of the limitations of previous models11,12,13,14,15,16.
Brain organoids are three-dimensional (3D), multicellular structures that emulate the main features of the cytoarchitecture and cell-type composition of one or multiple brain regions for a defined developmental time window11,12,13,14,17. These 3D structures are generated either from induced pluripotent stem cells (iPSCs) or, if available for the species of interest, from embryonic stem cells (ESCs). In general, two types of brain organoids can be distinguished based on the methodology used: unguided and regionalized (guided) brain organoids18. In generating the latter type of organoids, small molecules or factors are provided that guide the differentiation of the pluripotent stem cells to organoids of a particular brain region (e.g., forebrain organoids)18. By contrast, in unguided organoids, the differentiation is not guided by the addition of small molecules but rather relies exclusively on the spontaneous differentiation of the iPSCs/ESCs. The resulting brain organoids consist of cell types representing different brain regions (e.g., cerebral organoids)18. Brain organoids combine many key features of brain development with relatively cost- and time-efficient generation from any species of interest for which iPSCs or ESCs are available11,12,13,14. This makes brain organoids an excellent model for many kinds of neurobiological studies, ranging from evolutionary and developmental questions to disease modeling and drug testing15,16. However, addressing such questions using brain organoids strongly depends on the availability of different methods for genetic modification.
One key aspect of studying neocortex (patho)physiological development and its evolution is the functional analysis of genes and gene variants. This is usually achieved by (ectopic) expression and/or by knock-down (KD) or knock-out (KO) of those genes. Such genetic modifications can be classified into stable and transient genetic modification, as well as into the modifications being temporally and spatially restricted or not restricted. Stable genetic modification is defined by the introduction of a genetic alteration into the host genome that is passed on to all subsequent cell generations. Depending on the time point of genetic modification, it can affect all the cells of an organoid or can be restricted to certain cell populations. Most frequently, stable genetic modification is achieved in brain organoids at the iPSC/ESC level by applying lentiviruses, transposon-like systems, and the CRISPR/Cas9 technology (reviewed by, e.g., Fischer et al.17, Kyrousi et al.19, and Teriyapirom et al.20). This has the advantage that all cells of the brain organoid carry the genetic modification and that it is not temporally or spatially restricted. However, the generation and characterization of these stable iPSC/ESC lines are very time-consuming, often taking several months until the first modified brain organoids can be analyzed (reviewed by e.g., Fischer et al.17, Kyrousi et al.19, or Teriyapirom et al.20).
In contrast, transient genetic modification is defined by the delivery of genetic cargo (e.g., a gene expression plasmid) that does not integrate into the host genome. While this modification can, in principle, be passed on to subsequent cell generations, the delivered genetic cargo will be progressively diluted with each cell division. Therefore, this type of genetic modification is usually temporally and spatially restricted. Transient genetic modification can be carried out in brain organoids by adeno-associated viruses or by electroporation (reviewed by, e.g., Fischer et al.17, Kyrousi et al.19, and Teriyapirom et al.20), with the latter being described in detail in this article. In contrast to stable genetic modification, this approach is very fast and cost-efficient. Indeed, electroporation can be performed within minutes, and, depending on the target cell population(s), electroporated organoids are ready for analysis within days (reviewed by, e.g., Fischer et al.17 and Kyrousi et al.19). However, gross morphological changes of the brain organoid, such as differences in size, cannot be detected using this method, as this type of genetic modification is temporally and spatially restricted. This restriction can also be an advantage, for example, in the case of studying individual cell populations within the organoid or the effects on brain organoids at specific developmental time points (reviewed by, e.g., Fischer et al.17 and Kyrousi et al.19).
A classical approach to study gene function during brain development and evolution is in utero electroporation. In utero electroporation is a well-known and useful technique for the delivery of gene expression constructs into rodent21,22,23 and ferret24,25 brains. First, a solution containing the expression construct(s) of interest is microinjected through the uterine wall into a certain ventricle of the embryonic brain, depending on the region to be targeted. In the second step, electric pulses are applied to transfect the cells directly lining the targeted ventricle. This approach is not only limited to ectopic expression or the overexpression of genes, as it can also be applied in KD or KO studies by microinjecting short hairpin (shRNA) or CRISPR/Cas9 (in the form of expression plasmids or ribonucleoproteins [RNPs]), respectively26,27. However, the in utero electroporation of mouse, rat, and ferret embryos has the same limitations as described above for these animal models.
Ideally, one would like to perform in utero electroporation directly in primates. While this is, in principle, technically possible, in utero electroporation is not conducted in primates due to ethical concerns, high animal maintenance costs, and small litter sizes. For certain primates, such as great apes (including humans), this is not possible at all. However, these primates have the greatest potential for the study of human (patho)physiological neocortex development and its evolution. One solution to this dilemma is to apply the electroporation technique to primate brain organoids28.
This paper presents a protocol for the electroporation of a subtype of primate brain organoids, primate cerebral organoids. This approach allows the fast and cost-efficient genetic modification of cell populations within the ventricle-like structures of the organoids. Specifically, we describe a unified protocol for the generation of primate cerebral organoids from human (Homo sapiens), chimpanzee (Pan troglodytes), rhesus macaque (Macaca mulatta), and common marmoset (Callithrix jacchus) iPSCs. Moreover, we describe the microinjection and electroporation technique in detail and provide &#34;go&#34; and &#34;no-go&#34; criteria for performing primate cerebral organoid electroporation. This approach is an effective tool for studying (patho)physiological neocortex development and its evolution in a model especially close to the human situation.

Author Spotlight: Targeted Microinjection and Electroporation of Primate Cerebral Organoids for Genetic Modification  

Targeted Microinjection and Electroporation of Primate Cerebral Organoids for Genetic Modification

Our field of research is primate brain development and evolution. We are trying to understand the factors underlying neocortical expansion in primates. To address this question in a practical and ethically justifiable way, we use brain organoids as our research model.Differences in brain development between modern humans, us, and neanderthals have recently emerged. These differences are due to a small number of amino acid changes in proteins with key roles in brain development. Cerebral organoids have been a crucial model system in these studies.The study of primate development from an evolutionary point of view conducting gain and loss of function studies is important. However, apes including humans naturally cannot be used for such experiments, so genetic modification of organoids plays a vital role in this field. While working as a postdoc in my lab, Michael Heide demonstrated that the human specific gene ARHGAP11B was a key player in increasing brain size during human evolution.As a group leader at the German Primate Center now, Michael contributed crucial insight by comparing human versus chimpanzee cerebral organoids. Our protocol offers a targeted approach for genetic modifications by specific micro injecting ventricle-like structures instead of commercial electroporation cuvettes. This approach uses a cost efficient setup including square wave electroporator and Petri dish electrode chamber instead of expensive nuclear effector solutions.While studying function and brain development in primates by genetic modification is technically possible, it is methodologically demanding, expensive, and not allowed for great apes. The electroporation of primate cerebral organoids provides a fast and cost efficient approach to introduce genetic modifications in a model close to primate brain development. In the future, we would like to focus on the characterization of differentially expressed genes in the cortex of different primate species.We will study these genes by the electroporation of primate cerebral organoids and analyze their potential effects on cortical progenitor cells.

Watch this Scientific Journal Video about Generation of Cerebral Organoids from Primate-Induced Pluripotent Stem Cells IPSCs at JoVE.com

Generation of Cerebral Organoids from Primate-Induced Pluripotent Stem Cells (IPSCs)  

Generation of Cerebral Organoids from Primate-Induced Pluripotent Stem Cells (iPSCs)

To begin, wash the cultured iPSCs with Dulbecco's PBS or DPBS. And add one milliliter of proteolytic and collagenolytic mixture. Incubate the dish at 37 degrees Celsius for two minutes to detach the cells.Next, add 1.5 milliliters of prewarmed iPSC culture medium to stop the reaction. Dissociate the cells from the cell culture dish by pipetting up and down seven to 10 times to obtain a single-cell suspension. Transfer the cell suspension to a 15-milliliter conical centrifuge tube.Pellet the cells at 200xg for five minutes at room temperature. And aspirate the supernatant. Resuspend the pellet in two milliliters of iPSC culture medium supplemented with 50 micromolar Y27632.Now, use 10 microliters of the cell suspension to count the cells using a Neubauer chamber. Adjust the concentration of the cell suspension to 9, 000 cells per 150 microliters using iPSC culture medium supplemented with 50 micromolar Y27632. To generate embryoid bodies or EBs, shake the cell suspension tube to prevent cell sedimentation before seeding 150 microliters of the cell suspension into each well of an ultra-low attachment 96-well plate.Culture the EBs in a humified atmosphere for 48 hours. At the end of the incubation, remove 100 microliters of medium per well. And add 150 microliters of prewarmed fresh medium without Y27632.Create a four by four dimple grid on the parafilm by placing the parafilm grid on the 0.2 milliliter tube rack with the paper-enveloped side facing up. And gently press a gloved finger against each rack hole to embed the EBs in the basement membrane matrix. Then remove the paper and cut the dimple grid out of the parafilm square using scissors to adjust its size to fit into a 60-milliliter cell culture dish.Place the dimpled parafilm back on the 0.2 milliliter tube rack to provide a basis for the basement membrane matrix droplet generation. Carefully transfer the EBs one after another from the well of the culture dish to the parafilm dimples using a pipette with a cut 200 microliter pipette tip. After moving 16 EBs to the grid, take a new 200 microliters pipette tip and remove the remaining medium from the dimples.Now, pipette one drop of basement membrane matrix onto each dimple containing one EB.Take a 10-microliter pipette tip and quickly move the EBs into the center of each droplet without disturbing the droplet borders. Place the dimpled parafilm with the basement membrane matrix drops in a 60-millimeter cell culture dish. And incubate for 15 to 30 minutes at 37 degrees Celsius to allow the matrix to polymerize.Further, to detach the matrix-embedded EBs from the parafilm, add five milliliters of differentiation medium without vitamin A to the dish. And turn the parafilm square upside down using forceps so that the side with the EBs is facing the bottom of the dish. Carefully shake the dish to detach the basement membrane matrix drops containing the EBs from the parafilm.If some of them are still attached, take an edge of the parafilm square using forceps and rapidly roll it up toward the center of the dish multiple times. Then culture the cerebral organoids on an orbital shaker at 55 rpm in a humidified atmosphere with 5%carbon dioxide and 95%air at 37 degrees Celsius. Keep the organoids in DM without vitamin A with medium changes every other day.A brightfield image of a 32-day post-seeding human cerebral organoid with ventricle-like structures on the periphery and a compact, healthy morphology is shown.

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JoVE Journal

Developmental Biology

545 Görüntüleme.  German Primate Center, Leibniz Institute for Primate Research. Başlamak için, kültürlü iPSC'leri Dulbecco'nun PBS veya DPBS'si ile yıkayın. Ve bir mililitre proteolitik ve kollajenolitik karışım ekleyin. Hücreleri ayırmak için çanağı iki dakika boyunca 37 santigrat derecede inkübe edin.Daha sonra, reaksiyonu durdurmak için 1,5 mililitre önceden ısıtılmış iPSC kültür ortamı ekleyin. Tek hücreli bir süspansiyon elde etmek için hücreleri hücre kültürü kabından yedi ila 10 kez yukarı ve aşağı pipetleyerek ayır?...