Name: Electroporation of Primate Cerebral Organoids
Uploaded: 2023-03-24T12:10:00
Description: Watch this Scientific Journal Video about Electroporation of Primate Cerebral Organoids at JoVE.com

The video demonstrates a protocol for electroporation and microinjection of cerebral organoids. It includes steps for preparing electroporation mixes, injecting solutions, electroporating organoids, and assessing GFP-positive cells. The process highlights the examination of cell lineage and distribution in organoids over time, indicating the development of progenitor and neuronal cells.

electroporation of primate cerebral organoids

영장류 대뇌 오가노이드의 유전자 변형

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.

저자 스포트라이트: 유전자 변형을 위한 영장류 대뇌 오가노이드의 표적 미세주입 및 전기천공법  

유전자 변형을 위한 영장류 대뇌 오가노이드의 표적 미세주입 및 전기천공

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 Electroporation of Primate Cerebral Organoids at JoVE.com

Electroporation of Primate Cerebral Organoids  

영장류 대뇌 오가노이드의 전기천공법

대조군 및 관심 유전자를 위한 충분한 양의 전기천공 혼합물을 준비하는 것으로 시작합니다. 페트리 접시 전극 챔버를 전기 처리기에 연결합니다. 그런 다음 Microloader 팁을 사용하여 미세 주입 바늘에 각 전기 천공 혼합물 8마이크로리터를 채웁니다.미세한 가위를 사용하여 안정적인 흐름을 얻기 위해 사용하기 전에 바늘 끝을 자릅니다. 팁이 뭉툭하고 넓으면 오가노이드가 심하게 손상될 수 있으므로 팁의 작은 부분만 제거해야 합니다. 현미경으로 매끄러운 경계와 눈에 보이는 심실과 같은 구조를 가진 5개의 대뇌 오가노이드를 선택하십시오.그런 다음 1000마이크로리터 피펫 팁을 사용하여 예열된 DMEM/F-12가 들어 있는 35mm 세포 배양 접시로 옮깁니다. 이제 심실과 같은 구조의 벽을 통해 바늘을 조심스럽게 삽입하고 눈에 띄게 채워질 때까지 전기 천공 혼합물을 주입합니다. 파열을 방지하기 위해 심실과 같은 구조에 과도한 압력을 가하지 마십시오.미세주입된 대뇌 오가노이드 1개를 소량의 DMEM/F-12와 함께 페트리 접시 전극실로 옮깁니다. 미세 주입된 심실과 같은 구조의 표면이 전기 천공기의 양극에 연결된 전극을 향하도록 오가노이드를 배열합니다. 이제 1초 간격으로 각각 50밀리초 동안 80볼트의 펄스 5개를 사용하여 대뇌 오가노이드를 하나씩 전기천공합니다.비멸균 조건에서 미세주입 및 전기천공을 수행한 경우 층류 후드 아래에서 전기천공된 오가노이드를 예열된 DMEM/F-12로 채워진 새로운 35mm 세포 배양 접시로 옮깁니다. 그런 다음 섭씨 37도에서 5% 이산화탄소 및 95% 공기의 가습 분위기에서 55RPM의 궤도 셰이커에서 비타민 A와 함께 DM의 전기천공된 오가노이드를 배양합니다. 다음날, 전기천공 후, 기존의 도립 형광 현미경으로 성공적인 전기천공을 위해 대뇌 오가노이드를 확인합니다.절단된 1000마이크로리터 피펫 팁을 사용하여 전기천공된 오가노이드를 15밀리리터 원추형 원심분리기 튜브로 옮기고 초과 배지를 제거합니다. DPBS에 충분한 양의 4% 파라포름알데히드를 첨가하고 실온에서 30분 동안 배양합니다. 배양이 끝나면 파라 포름 알데히드를 흡인하십시오.그런 다음 5밀리리터의 DPBS를 넣고 부드럽게 흔들어 DPBS를 흡인합니다. 오가노이드는 나중에 사용할 때까지 섭씨 4도의 DPBS에 보관하십시오. 전기천공 이틀 후, GFP 양성 세포는 거의 독점적으로 심실 영역에 국한되어 있고 Pax6에 대해 양성이며, 이는 이들 세포가 정점 전구체 또는 신생아 기저 전구체임을 나타냅니다.10 일 후, GFP 양성 세포는 기저 부위에 국한됩니다. 이 세포는 또한 Pax6 또는 NeuN에 대해 양성이며, 이는 각각 기저 전구체 또는 뉴런을 나타냅니다. GFP 양성 세포의 3차원 분포의 인상을 얻기 위해 전기천공된 대뇌 오가노이드의 3차원 재구성이 도시되어 있다.

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JoVE Journal

Developmental Biology

Electroporation of Primate Cerebral Organoids

Targeted Microinjection and Electroporation of Primate Cerebral Organoids for Genetic Modification

The cerebral cortex is the outermost brain structure and is responsible for the processing of sensory input and motor output; it is seen as the seat of ...