Long term non-invasive imaging of embryonic stem cells using reporter genes.

Abstract:

:Development of non-invasive and accurate methods to track cell fate after delivery will greatly expedite transition of embryonic stem (ES) cell therapy to the clinic. In this protocol, we describe the in vivo monitoring of stem cell survival, proliferation and migration using reporter genes. We established stable ES cell lines constitutively expressing double fusion (DF; enhanced green fluorescent protein and firefly luciferase) or triple fusion (TF; monomeric red fluorescent protein, firefly luciferase and herpes simplex virus thymidine kinase (HSVtk)) reporter genes using lentiviral transduction. We used fluorescence-activated cell sorting to purify these populations in vitro, bioluminescence imaging and positron emission tomography (PET) imaging to track them in vivo and fluorescence immunostaining to confirm the results ex vivo. Unlike other methods of cell tracking, such as iron particle and radionuclide labeling, reporter genes are inherited genetically and can be used to monitor cell proliferation and survival for the lifetime of transplanted cells and their progeny.

journal_name

Nat Protoc

journal_title

Nature protocols

authors

Sun N,Lee A,Wu JC

doi

10.1038/nprot.2009.100

subject

Has Abstract

pub_date

2009-01-01 00:00:00

pages

1192-201

issue

8

eissn

1754-2189

issn

1750-2799

pii

nprot.2009.100

journal_volume

4

pub_type

杂志文章
  • Video tracking and analysis of sleep in Drosophila melanogaster.

    abstract::In the past decade, Drosophila has emerged as an ideal model organism for studying the genetic components of sleep as well as its regulation and functions. In fruit flies, sleep can be conveniently estimated by measuring the locomotor activity of the flies using techniques and instruments adapted from the field of cir...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2012.041

    authors: Gilestro GF

    更新日期:2012-04-26 00:00:00

  • 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

  • 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

  • Spheroid-based human endothelial cell microvessel formation in vivo.

    abstract::The study of angiogenic endothelial cells (ECs) has in recent years greatly stimulated multiple fields of vascular biology research. A number of cellular models and numerous complex developmental, manipulatory and tumor animal models have been developed to study angiogenesis in vitro and in vivo. To connect the versat...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2009.96

    authors: Laib AM,Bartol A,Alajati A,Korff T,Weber H,Augustin HG

    更新日期:2009-01-01 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

  • 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 rapid micro chromatin immunoprecipitation assay (microChIP).

    abstract::Interactions of proteins with DNA mediate many critical nuclear functions. Chromatin immunoprecipitation (ChIP) is a robust technique for studying protein-DNA interactions. Current ChIP assays, however, either require large cell numbers, which prevent their application to rare cell samples or small-tissue biopsies, or...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2008.68

    authors: Dahl JA,Collas P

    更新日期:2008-01-01 00:00:00

  • Coupling surface plasmon resonance to mass spectrometry to discover novel protein-protein interactions.

    abstract::The elucidation of protein-protein interaction networks is a crucial task in the postgenomic era. In this protocol, we describe our approach to discover protein-protein interactions using the surface plasmon resonance technique coupled to mass spectrometry (MS). A peptide or a protein is immobilized on a sensor chip a...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2009.84

    authors: Madeira A,Ohman E,Nilsson A,Sjögren B,Andrén PE,Svenningsson P

    更新日期:2009-01-01 00:00:00

  • Investigation of higher-order RNA G-quadruplex structures in vitro and in living cells by 19F NMR spectroscopy.

    abstract::Growing evidence indicates that RNA G-quadruplexes have important roles in various processes such as transcription, translation, regulation of telomere length, and formation of telomeric heterochromatin. Investigation of RNA G-quadruplex structures associated with biological events is therefore essential to understand...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2017.156

    authors: Bao HL,Xu Y

    更新日期:2018-04-01 00:00:00

  • Single nucleotide polymorphism detection by polymerase chain reaction-restriction fragment length polymorphism.

    abstract::Accurate analysis of DNA sequence variation in not only humans and animals but also other organisms has played a significant role in expanding our knowledge about genetic variety and diversity in a number of different biological areas. The search for an understanding of the causes of genetic variants and mutations has...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2007.407

    authors: Ota M,Fukushima H,Kulski JK,Inoko H

    更新日期:2007-01-01 00:00:00

  • Scototaxis as anxiety-like behavior in fish.

    abstract::The scototaxis (dark/light preference) protocol is a behavioral model for fish that is being validated to assess the antianxiety effects of pharmacological agents and the behavioral effects of toxic substances, and to investigate the (epi)genetic bases of anxiety-related behavior. Briefly, a fish is placed in a centra...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2009.225

    authors: Maximino C,Marques de Brito T,Dias CA,Gouveia A Jr,Morato S

    更新日期:2010-02-01 00:00:00

  • In vivo two-photon imaging of sensory-evoked dendritic calcium signals in cortical neurons.

    abstract::Neurons in cortical sensory regions receive modality-specific information through synapses that are located on their dendrites. Recently, the use of two-photon microscopy combined with whole-cell recordings has helped to identify visually evoked dendritic calcium signals in mouse visual cortical neurons in vivo. The c...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2010.169

    authors: Jia H,Rochefort NL,Chen X,Konnerth A

    更新日期:2011-01-01 00:00:00

  • A practical guide to adaptive light-sheet microscopy.

    abstract::We describe the implementation and use of an adaptive imaging framework for optimizing spatial resolution and signal strength in a light-sheet microscope. The framework, termed AutoPilot, comprises hardware and software modules for automatically measuring and compensating for mismatches between light-sheet and detecti...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/s41596-018-0043-4

    authors: Royer LA,Lemon WC,Chhetri RK,Keller PJ

    更新日期:2018-11-01 00:00:00

  • Multiplexed array-based and in-solution genomic enrichment for flexible and cost-effective targeted next-generation sequencing.

    abstract::The unprecedented increase in the throughput of DNA sequencing driven by next-generation technologies now allows efficient analysis of the complete protein-coding regions of genomes (exomes) for multiple samples in a single sequencing run. However, sample preparation and targeted enrichment of multiple samples has bec...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2011.396

    authors: Harakalova M,Mokry M,Hrdlickova B,Renkens I,Duran K,van Roekel H,Lansu N,van Roosmalen M,de Bruijn E,Nijman IJ,Kloosterman WP,Cuppen E

    更新日期:2011-11-03 00:00:00

  • Single-stranded DNA library preparation for the sequencing of ancient or damaged DNA.

    abstract::This protocol describes a method for converting short single-stranded and double-stranded DNA into libraries compatible with high-throughput sequencing using Illumina technology. This method has primarily been developed to improve sequence retrieval from ancient DNA, but it is also applicable to the sequencing of shor...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2013.038

    authors: Gansauge MT,Meyer M

    更新日期:2013-04-01 00:00:00

  • Measurement of proliferation and disappearance of rapid turnover cell populations in human studies using deuterium-labeled glucose.

    abstract::Cell proliferation may be measured in vivo by quantifying DNA synthesis with isotopically labeled deoxyribonucleotide precursors. Deuterium-labeled glucose is one such precursor which, because it achieves high levels of enrichment for a short period, is well suited to the study of rapidly dividing cells, in contrast t...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2009.117

    authors: Macallan DC,Asquith B,Zhang Y,de Lara C,Ghattas H,Defoiche J,Beverley PC

    更新日期:2009-01-01 00:00:00

  • Holographic two-photon activation for synthetic optogenetics.

    abstract::Optogenetic tools provide users the ability to photocontrol the activity of cells. Commonly, activation is achieved by expression of proteins from photosynthetic organisms, for example, microbial opsins (e.g., ChR2). Alternatively, a sister approach, synthetic optogenetics, enables photocontrol over proteins of mammal...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/s41596-018-0118-2

    authors: Carmi I,De Battista M,Maddalena L,Carroll EC,Kienzler MA,Berlin S

    更新日期:2019-03-01 00:00:00

  • High-throughput identification of proteins with AMPylation using self-assembled human protein (NAPPA) microarrays.

    abstract::AMPylation (adenylylation) has been recognized as an important post-translational modification that is used by pathogens to regulate host cellular proteins and their associated signaling pathways. AMPylation has potential functions in various cellular processes, and it is widely conserved across both prokaryotes and e...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2015.044

    authors: Yu X,LaBaer J

    更新日期:2015-05-01 00:00:00

  • Fluorescence resonance energy transfer microscopy as demonstrated by measuring the activation of the serine/threonine kinase Akt.

    abstract::This protocol describes procedures for performing fluorescence resonance energy transfer (FRET) microscopy analysis by three different methods: acceptor photobleaching, sensitized emission and spectral imaging. We also discuss anisotropy and fluorescence lifetime imaging microscopy-based FRET techniques. By using the ...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2012.147

    authors: Broussard JA,Rappaz B,Webb DJ,Brown CM

    更新日期:2013-02-01 00:00:00

  • 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...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2013.106

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

    更新日期:2013-09-01 00:00:00

  • Fluid-percussion-induced traumatic brain injury model in rats.

    abstract::Traumatic brain injury (TBI) is a major cause of mortality and morbidity. Various attempts have been made to replicate clinical TBI using animal models. The fluid-percussion model (FP) is one of the oldest and most commonly used models of experimentally induced TBI. Both central (CFP) and lateral (LFP) variations of t...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2010.112

    authors: Kabadi SV,Hilton GD,Stoica BA,Zapple DN,Faden AI

    更新日期:2010-09-01 00:00:00

  • Site-specific protein labeling using PRIME and chelation-assisted click chemistry.

    abstract::This protocol describes an efficient method to site-specifically label cell-surface or purified proteins with chemical probes in two steps: probe incorporation mediated by enzymes (PRIME) followed by chelation-assisted copper-catalyzed azide-alkyne cycloaddition (CuAAC). In the PRIME step, Escherichia coli lipoic acid...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2013.096

    authors: Uttamapinant C,Sanchez MI,Liu DS,Yao JZ,Ting AY

    更新日期:2013-08-01 00:00:00

  • A mass spectrometry workflow for measuring protein turnover rates in vivo.

    abstract::Proteins are continually produced and degraded, to avoid the accumulation of old or damaged molecules and to maintain the efficiency of physiological processes. Despite its importance, protein turnover has been difficult to measure in vivo. Previous approaches to evaluating turnover in vivo have required custom labeli...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/s41596-019-0222-y

    authors: Alevra M,Mandad S,Ischebeck T,Urlaub H,Rizzoli SO,Fornasiero EF

    更新日期:2019-12-01 00:00:00

  • Standardized bacteriophage purification for personalized phage therapy.

    abstract::The world is on the cusp of a post-antibiotic era, but researchers and medical doctors have found a way forward-by looking back at how infections were treated before the advent of antibiotics, namely using phage therapy. Although bacteriophages (phages) continue to lack drug approval in Western medicine, an increasing...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/s41596-020-0346-0

    authors: Luong T,Salabarria AC,Edwards RA,Roach DR

    更新日期:2020-09-01 00:00:00

  • Synthesis of oligo-RNAs with photocaged adenosine 2'-hydroxyls.

    abstract::This protocol describes a general method for the preparation of RNAs in which the reactivity or hydrogen-bonding properties of the molecule are modified in a photoreversible fashion by use of a caging strategy. A single caged adenosine, modified at the 2' position as a nitro-benzyl ether, can be incorporated into shor...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2007.154

    authors: Chaulk SG,MacMillan AM

    更新日期:2007-01-01 00:00:00

  • Population-specific genotype imputations using minimac or IMPUTE2.

    abstract::In order to meaningfully analyze common and rare genetic variants, results from genome-wide association studies (GWASs) of multiple cohorts need to be combined in a meta-analysis in order to obtain enough power. This requires all cohorts to have the same single-nucleotide polymorphisms (SNPs) in their GWASs. To this e...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2015.077

    authors: van Leeuwen EM,Kanterakis A,Deelen P,Kattenberg MV,Genome of the Netherlands Consortium.,Slagboom PE,de Bakker PI,Wijmenga C,Swertz MA,Boomsma DI,van Duijn CM,Karssen LC,Hottenga JJ

    更新日期:2015-09-01 00:00:00

  • An experimental murine model to study periodontitis.

    abstract::Periodontal disease (PD) is a common dental disease associated with the interaction between dysbiotic oral microbiota and host immunity. It is a prevalent disease, resulting in loss of gingival tissue, periodontal ligament, cementum and alveolar bone. PD is a major form of tooth loss in the adult population. Experimen...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/s41596-018-0035-4

    authors: Marchesan J,Girnary MS,Jing L,Miao MZ,Zhang S,Sun L,Morelli T,Schoenfisch MH,Inohara N,Offenbacher S,Jiao Y

    更新日期:2018-10-01 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

  • Microfluidic mixer designed for performing single-molecule kinetics with confocal detection on timescales from milliseconds to minutes.

    abstract::Microfluidic mixing in combination with single-molecule spectroscopy allows the investigation of complex biomolecular processes under non-equilibrium conditions. Here we present a protocol for building, installing and operating microfluidic mixing devices optimized for this purpose. The mixer is fabricated by replica ...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2013.082

    authors: Wunderlich B,Nettels D,Benke S,Clark J,Weidner S,Hofmann H,Pfeil SH,Schuler B

    更新日期:2013-08-01 00:00:00

  • Live visualization of protein synthesis in axonal growth cones by microinjection of photoconvertible Kaede into Xenopus embryos.

    abstract::Photoconvertible fluorescent proteins, such as Kaede, can be switched irreversibly from their native color to a new one. This property can be exploited to visualize de novo mRNA translation, because newly synthesized proteins can be distinguished from preexisting ones by their color. In this protocol, Kaede cDNA linke...

    journal_title:Nature protocols

    pub_type: 杂志文章

    doi:10.1038/nprot.2008.113

    authors: Leung KM,Holt CE

    更新日期:2008-01-01 00:00:00