Directed differentiation of forebrain GABA interneurons from human pluripotent stem cells.

Abstract:

:Forebrain γ-aminobutyric acid (GABA) interneurons have crucial roles in high-order brain function via modulating network activities and plasticity, and they are implicated in many psychiatric disorders. Availability of enriched functional human forebrain GABA interneurons, especially those from people affected by GABA interneuron deficit disease, will be instrumental to the investigation of disease pathogenesis and development of therapeutics. We describe a protocol for directed differentiation of forebrain GABA interneurons from human embryonic stem cells (ESCs) and induced pluripotent stem cells (iPSCs) in a chemically defined system. In this protocol, human PSCs are first induced to primitive neuroepithelial cells over 10 d, and then patterned to NKX2.1-expressing medial ganglionic eminence progenitors by simple treatment with sonic hedgehog or its agonist purmorphamine over the next 2 weeks. These progenitors generate a nearly pure population of forebrain GABA interneurons by the sixth week. This simple and efficient protocol does not require transgenic modification or cell sorting, and it has been replicated with multiple human ESC and iPSC lines.

journal_name

Nat Protoc

journal_title

Nature protocols

authors

Liu Y,Liu H,Sauvey C,Yao L,Zarnowska ED,Zhang SC

doi

10.1038/nprot.2013.106

subject

Has Abstract

pub_date

2013-09-01 00:00:00

pages

1670-9

issue

9

eissn

1754-2189

issn

1750-2799

pii

nprot.2013.106

journal_volume

8

pub_type

杂志文章
  • Reverse transfection on cell arrays for high content screening microscopy.

    abstract::Here, we describe a robust protocol for the reverse transfection of cells on small interfering (siRNA) arrays, which, in combination with multi-channel immunofluorescence or time-lapse microscopy, is suitable for genome-wide RNA interference (RNAi) screens in intact human cells. The automatic production of 48 'transfe...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2006.483

    authors: Erfle H,Neumann B,Liebel U,Rogers P,Held M,Walter T,Ellenberg J,Pepperkok R

    更新日期:2007-01-01 00:00:00

  • Transformation of the rodent malaria parasite Plasmodium chabaudi.

    abstract::The rodent malaria parasite Plasmodium chabaudi chabaudi shares many features with human malaria species, including P. falciparum, and is the in vivo model of choice for many aspects of malaria research in the mammalian host, from sequestration of parasitized erythrocytes, to antigenic variation and host immunity and ...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2011.313

    authors: Spence PJ,Cunningham D,Jarra W,Lawton J,Langhorne J,Thompson J

    更新日期:2011-04-01 00:00:00

  • High-yield and high-purity isolation of hepatic stellate cells from normal and fibrotic mouse livers.

    abstract::Hepatic stellate cells (HSCs) have been identified as the main fibrogenic cell type in the liver. Hence, efforts to understand hepatic fibrogenesis and to develop treatment strategies have focused on this cell type. HSC isolation, originally developed in rats, has subsequently been adapted to mice, thus allowing the s...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2015.017

    authors: Mederacke I,Dapito DH,Affò S,Uchinami H,Schwabe RF

    更新日期:2015-02-01 00:00:00

  • CRISPR-Cas9-mediated genome editing in apple and grapevine.

    abstract::The CRISPR-Cas9 genome-editing tool and the availability of whole-genome sequences from plant species have revolutionized our ability to introduce targeted mutations into important crop plants, both to explore genetic changes and to introduce new functionalities. Here, we describe protocols adapting the CRISPR-Cas9 sy...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/s41596-018-0067-9

    authors: Osakabe Y,Liang Z,Ren C,Nishitani C,Osakabe K,Wada M,Komori S,Malnoy M,Velasco R,Poli M,Jung MH,Koo OJ,Viola R,Nagamangala Kanchiswamy C

    更新日期:2018-12-01 00:00:00

  • Isolation of DNA from small amounts of elephant ivory.

    abstract::This protocol describes a method for the extraction of DNA from elephant ivory. These techniques are being used to assign geographic origin to poached ivory by comparing the ivory genotype to a geographic-based gene frequency map, developed separately. The method has three components: ivory pulverization, decalcificat...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2007.318

    authors: Mailand C,Wasser SK

    更新日期:2007-01-01 00:00:00

  • A generic protocol for the expression and purification of recombinant RNA in Escherichia coli using a tRNA scaffold.

    abstract::RNA production using in vivo transcription by Escherichia coli allows preparation of milligram quantities of RNA for biochemical, biophysical and structural investigations. We describe here a generic protocol for the overproduction and purification of recombinant RNA using liquid chromatography. The strategy utilizes ...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2009.67

    authors: Ponchon L,Beauvais G,Nonin-Lecomte S,Dardel F

    更新日期:2009-01-01 00:00:00

  • A simple and rapid nonviral approach to efficiently transfect primary tissue-derived cells using polyethylenimine.

    abstract::This protocol outlines steps for optimizing the transfection of adherent primary mammalian cells using the readily available off-the-shelf cationic polymer, 25-kDa branched polyethylenimine (bPEI25). Transfection efficiency of cationic polymers varies among cell lines and is highly dependent on the conditions and envi...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2012.038

    authors: Hsu CY,Uludağ H

    更新日期:2012-04-19 00:00:00

  • Oxidative bisulfite sequencing of 5-methylcytosine and 5-hydroxymethylcytosine.

    abstract::To uncover the function of and interplay between the mammalian cytosine modifications 5-methylcytosine (5mC) and 5-hydroxymethylcytosine (5hmC), new techniques and advances in current technology are needed. To this end, we have developed oxidative bisulfite sequencing (oxBS-seq), which can quantitatively locate 5mC an...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2013.115

    authors: Booth MJ,Ost TW,Beraldi D,Bell NM,Branco MR,Reik W,Balasubramanian S

    更新日期:2013-10-01 00:00:00

  • A ring barrier-based migration assay to assess cell migration in vitro.

    abstract::Cell migration is a key feature of virtually every biological process, and it can be studied in a variety of ways. Here we outline a protocol for the in vitro study of cell migration using a ring barrier-based assay. A 'barrier' is inserted in the culture chamber, which prevents cells from entering a defined area. Cel...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2015.056

    authors: Das AM,Eggermont AM,ten Hagen TL

    更新日期:2015-06-01 00:00:00

  • Generation of high-purity human ventral midbrain dopaminergic progenitors for in vitro maturation and intracerebral transplantation.

    abstract::Generation of precisely patterned neural cells from human pluripotent stem cells (hPSCs) is instrumental in developing disease models and stem cell therapies. Here, we provide a detailed 16-d protocol for obtaining high-purity ventral midbrain (VM) dopamine (DA) progenitors for intracerebral transplantation into anima...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2017.078

    authors: Nolbrant S,Heuer A,Parmar M,Kirkeby A

    更新日期:2017-09-01 00:00:00

  • τ-SGA: synthetic genetic array analysis for systematically screening and quantifying trigenic interactions in yeast.

    abstract::Systematic complex genetic interaction studies have provided insight into high-order functional redundancies and genetic network wiring of the cell. Here, we describe a method for screening and quantifying trigenic interactions from ordered arrays of yeast strains grown on agar plates as individual colonies. The proto...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/s41596-020-00456-3

    authors: Kuzmin E,Rahman M,VanderSluis B,Costanzo M,Myers CL,Andrews BJ,Boone C

    更新日期:2021-01-18 00:00:00

  • Fluorometric measurement of nitrite/nitrate by 2,3-diaminonaphthalene.

    abstract::We describe a step-by-step protocol for measuring the stable products of the nitric oxide (NO) pathway: nitrite, nitrite plus nitrate and nitrate. This described protocol is easy to apply and is about 50 times more sensitive than the commonly used Griess reaction or commercially available assay kits based on the Gries...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2006.341

    authors: Nussler AK,Glanemann M,Schirmeier A,Liu L,Nüssler NC

    更新日期:2006-01-01 00:00:00

  • In vivo models of proliferative vitreoretinopathy.

    abstract::We outline current in vitro and in vivo models for experimental proliferative vitreoretinopathy (PVR) and provide a detailed protocol of our standardized in vivo PVR model. PVR is the leading cause of failed surgical procedures for the correction of rhegmatogenous retinal detachment. The pathogenesis of this multifact...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2007.4

    authors: Agrawal RN,He S,Spee C,Cui JZ,Ryan SJ,Hinton DR

    更新日期:2007-01-01 00:00:00

  • Preparation of aptamer-linked gold nanoparticle purple aggregates for colorimetric sensing of analytes.

    abstract::Aptamers are single-stranded DNA or RNA molecules that can bind target molecules with high affinity and specificity. The conformation of an aptamer usually changes upon binding to its target analyte, and this property has been used in a wide variety of sensing applications, including detection based on fluorescence in...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2006.38

    authors: Liu J,Lu Y

    更新日期:2006-01-01 00:00:00

  • Microwave-assisted synthesis of triple-helical, collagen-mimetic lipopeptides.

    abstract::Collagen-mimetic peptides and lipopeptides are widely used as substrates for matrix degrading enzymes, as new biomaterials for tissue engineering, as drug delivery systems and so on. However, the preparation and subsequent purification of these peptides and their fatty-acid conjugates are really challenging. Herein, w...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2009.195

    authors: Banerjee J,Hanson AJ,Muhonen WW,Shabb JB,Mallik S

    更新日期:2010-01-01 00:00:00

  • Analysis of neurotransmitter release mechanisms by photolysis of caged Ca²⁺ in an autaptic neuron culture system.

    abstract::Neurotransmitter release is triggered by membrane depolarization, Ca(2+) influx and Ca(2+) sensing by the release machinery, causing synaptic vesicle (SV) fusion with the plasma membrane. Interlinked is a complex membrane cycle in which vesicles are tethered to the release site, primed, fused and recycled. As many of ...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2012.074

    authors: Burgalossi A,Jung S,Man KN,Nair R,Jockusch WJ,Wojcik SM,Brose N,Rhee JS

    更新日期:2012-06-21 00:00:00

  • Advanced CUBIC protocols for whole-brain and whole-body clearing and imaging.

    abstract::Here we describe a protocol for advanced CUBIC (Clear, Unobstructed Brain/Body Imaging Cocktails and Computational analysis). The CUBIC protocol enables simple and efficient organ clearing, rapid imaging by light-sheet microscopy and quantitative imaging analysis of multiple samples. The organ or body is cleared by im...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2015.085

    authors: Susaki EA,Tainaka K,Perrin D,Yukinaga H,Kuno A,Ueda HR

    更新日期:2015-11-01 00:00:00

  • Rapid bacterial artificial chromosome modification for large-scale mouse transgenesis.

    abstract::We report here a high-throughput method for the modification of bacterial artificial chromosomes (BACs) that uses a novel two-plasmid approach. In this protocol, a vector modified in our laboratory to hold an R6Kγ origin of replication and a marker recombination cassette is inserted into a BAC in a single recombinatio...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2010.131

    authors: Gong S,Kus L,Heintz N

    更新日期:2010-09-01 00:00:00

  • Generation of lung organoids from human pluripotent stem cells in vitro.

    abstract::The lung epithelium is derived from the endodermal germ layer, which undergoes a complex series of endoderm-mesoderm-mediated signaling events to generate the final arborized network of conducting airways (bronchi, bronchioles) and gas-exchanging units (alveoli). These stages include endoderm induction, anterior-poste...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/s41596-018-0104-8

    authors: Miller AJ,Dye BR,Ferrer-Torres D,Hill DR,Overeem AW,Shea LD,Spence JR

    更新日期:2019-02-01 00:00:00

  • Visualization of protein interactions in living Caenorhabditis elegans using bimolecular fluorescence complementation analysis.

    abstract::The bimolecular fluorescence complementation (BiFC) assay is a powerful tool for visualizing and identifying protein interactions in living cells. This assay is based on the principle of protein-fragment complementation, using two nonfluorescent fragments derived from fluorescent proteins. When two fragments are broug...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2008.16

    authors: Shyu YJ,Hiatt SM,Duren HM,Ellis RE,Kerppola TK,Hu CD

    更新日期:2008-01-01 00:00:00

  • A cell-free organelle-based in vitro system for studying the peroxisomal protein import machinery.

    abstract::Here we describe a protocol to dissect the peroxisomal matrix protein import pathway using a cell-free in vitro system. The system relies on a postnuclear supernatant (PNS), which is prepared from rat/mouse liver, to act as a source of peroxisomes and cytosolic components. A typical in vitro assay comprises the follow...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2016.147

    authors: Rodrigues TA,Francisco T,Dias AF,Pedrosa AG,Grou CP,Azevedo JE

    更新日期:2016-12-01 00:00:00

  • Cryopreservation and banking of mammalian cell lines.

    abstract::This protocol describes the principles and methods used for the preparation of cryopreserved cell stocks. Following these procedures will ensure the availability of reproducible cultures for use within a single laboratory at different times and for different collaborating laboratories. Although the basic principle is ...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2008.190

    authors: Stacey GN,Masters JR

    更新日期:2008-01-01 00:00:00

  • 5' end-centered expression profiling using cap-analysis gene expression and next-generation sequencing.

    abstract::Cap-analysis gene expression (CAGE) provides accurate high-throughput measurement of RNA expression. CAGE allows mapping of all the initiation sites of both capped coding and noncoding RNAs. In addition, transcriptional start sites within promoters are characterized at single-nucleotide resolution. The latter allows t...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2012.005

    authors: Takahashi H,Lassmann T,Murata M,Carninci P

    更新日期:2012-02-23 00:00:00

  • Miniaturized parallel screens to identify chromatographic steps required for recombinant protein purification.

    abstract::Methods development in chromatography is a time-consuming, trial-and-error process that requires laborious experimentation. We describe a high-throughput screening (HTS) protocol for the rapid identification of chromatographic steps for protein purification from cell-free expression broths. Broths containing the prote...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2009.149

    authors: Rege K,Heng M

    更新日期:2010-03-01 00:00:00

  • High spatial resolution imaging of biological tissues using nanospray desorption electrospray ionization mass spectrometry.

    abstract::Mass spectrometry imaging (MSI) enables label-free spatial mapping of hundreds of biomolecules in tissue sections. This capability provides valuable information on tissue heterogeneity that is difficult to obtain using population-averaged assays. Despite substantial developments in both instrumentation and methodology...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/s41596-019-0237-4

    authors: Yin R,Burnum-Johnson KE,Sun X,Dey SK,Laskin J

    更新日期:2019-12-01 00:00:00

  • Quantitative assessment of RNA-protein interactions with high-throughput sequencing-RNA affinity profiling.

    abstract::Because RNA-protein interactions have a central role in a wide array of biological processes, methods that enable a quantitative assessment of these interactions in a high-throughput manner are in great demand. Recently, we developed the high-throughput sequencing-RNA affinity profiling (HiTS-RAP) assay that couples s...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2015.074

    authors: Ozer A,Tome JM,Friedman RC,Gheba D,Schroth GP,Lis JT

    更新日期:2015-08-01 00:00:00

  • A protocol for isolation and culture of mesenchymal stem cells from mouse compact bone.

    abstract::Unlike humans, mouse bone marrow-derived mesenchymal stem cells (MSCs) cannot be easily harvested by adherence to plastic owing to the contamination of cultures by hematopoietic cells. The design of the protocol described here is based on the phenomenon that compact bones abound in MSCs and hematopoietic cells exist i...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2009.238

    authors: Zhu H,Guo ZK,Jiang XX,Li H,Wang XY,Yao HY,Zhang Y,Mao N

    更新日期:2010-03-01 00:00:00

  • Long-read sequencing data analysis for yeasts.

    abstract::Long-read sequencing technologies have become increasingly popular due to their strengths in resolving complex genomic regions. As a leading model organism with small genome size and great biotechnological importance, the budding yeast Saccharomyces cerevisiae has many isolates currently being sequenced with long read...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2018.025

    authors: Yue JX,Liti G

    更新日期:2018-06-01 00:00:00

  • Development of a highly reproducible three-dimensional organotypic model of the oral mucosa.

    abstract::In this report we describe the development of a standardized three-dimensional (3D) system of the human oral mucosa based on an immortalized human oral keratinocyte cell line (OKF6/TERT-2). The procedure takes approximately 2-3 weeks to complete and includes three main stages: preparation of collagen-embedded fibrobla...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2006.323

    authors: Dongari-Bagtzoglou A,Kashleva H

    更新日期:2006-01-01 00:00:00

  • Using TTchem-seq for profiling nascent transcription and measuring transcript elongation.

    abstract::The dynamics of transcription can be studied genome wide by high-throughput sequencing of nascent and newly synthesized RNA. 4-thiouridine (4SU) labeling in vivo enables the specific capture of such new transcripts, with 4SU residues being tagged by biotin linkers and captured using streptavidin beads before library p...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/s41596-019-0262-3

    authors: Gregersen LH,Mitter R,Svejstrup JQ

    更新日期:2020-02-01 00:00:00