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  1. Article ; Online: Mitochondrial single-cell ATAC-seq for high-throughput multi-omic detection of mitochondrial genotypes and chromatin accessibility.

    Lareau, Caleb A / Liu, Vincent / Muus, Christoph / Praktiknjo, Samantha D / Nitsch, Lena / Kautz, Pauline / Sandor, Katalin / Yin, Yajie / Gutierrez, Jacob C / Pelka, Karin / Satpathy, Ansuman T / Regev, Aviv / Sankaran, Vijay G / Ludwig, Leif S

    Nature protocols

    2023  Volume 18, Issue 5, Page(s) 1416–1440

    Abstract: Natural sequence variation within mitochondrial DNA (mtDNA) contributes to human phenotypes and may serve as natural genetic markers in human cells for clonal and lineage tracing. We recently developed a single-cell multi-omic approach, called ' ... ...

    Abstract Natural sequence variation within mitochondrial DNA (mtDNA) contributes to human phenotypes and may serve as natural genetic markers in human cells for clonal and lineage tracing. We recently developed a single-cell multi-omic approach, called 'mitochondrial single-cell assay for transposase-accessible chromatin with sequencing' (mtscATAC-seq), enabling concomitant high-throughput mtDNA genotyping and accessible chromatin profiling. Specifically, our technique allows the mitochondrial genome-wide inference of mtDNA variant heteroplasmy along with information on cell state and accessible chromatin variation in individual cells. Leveraging somatic mtDNA mutations, our method further enables inference of clonal relationships among native ex vivo-derived human cells not amenable to genetic engineering-based clonal tracing approaches. Here, we provide a step-by-step protocol for the use of mtscATAC-seq, including various cell-processing and flow cytometry workflows, by using primary hematopoietic cells, subsequent single-cell genomic library preparation and sequencing that collectively take ~3-4 days to complete. We discuss experimental and computational data quality control metrics and considerations for the extension to other mammalian tissues. Overall, mtscATAC-seq provides a broadly applicable platform to map clonal relationships between cells in human tissues, investigate fundamental aspects of mitochondrial genetics and enable additional modes of multi-omic discovery.
    MeSH term(s) Animals ; Humans ; Chromatin/genetics ; Chromatin Immunoprecipitation Sequencing ; Multiomics ; Sequence Analysis, DNA/methods ; High-Throughput Nucleotide Sequencing/methods ; DNA, Mitochondrial/genetics ; Genotype ; Mammals/genetics
    Chemical Substances Chromatin ; DNA, Mitochondrial
    Language English
    Publishing date 2023-02-15
    Publishing country England
    Document type Journal Article ; Review ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2244966-8
    ISSN 1750-2799 ; 1754-2189
    ISSN (online) 1750-2799
    ISSN 1754-2189
    DOI 10.1038/s41596-022-00795-3
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Positional influence on cellular transcriptional identity revealed through spatially segmented single-cell transcriptomics.

    Morse, David B / Michalowski, Aleksandra M / Ceribelli, Michele / De Jonghe, Joachim / Vias, Maria / Riley, Deanna / Davies-Hill, Theresa / Voss, Ty / Pittaluga, Stefania / Muus, Christoph / Liu, Jiamin / Boyle, Samantha / Weitz, David A / Brenton, James D / Buenrostro, Jason D / Knowles, Tuomas P J / Thomas, Craig J

    Cell systems

    2023  Volume 14, Issue 6, Page(s) 464–481.e7

    Abstract: Single-cell RNA sequencing (scRNA-seq) is a powerful technique for describing cell states. Identifying the spatial arrangement of these states in tissues remains challenging, with the existing methods requiring niche methodologies and expertise. Here, we ...

    Abstract Single-cell RNA sequencing (scRNA-seq) is a powerful technique for describing cell states. Identifying the spatial arrangement of these states in tissues remains challenging, with the existing methods requiring niche methodologies and expertise. Here, we describe segmentation by exogenous perfusion (SEEP), a rapid and integrated method to link surface proximity and environment accessibility to transcriptional identity within three-dimensional (3D) disease models. The method utilizes the steady-state diffusion kinetics of a fluorescent dye to establish a gradient along the radial axis of disease models. Classification of sample layers based on dye accessibility enables dissociated and sorted cells to be characterized by transcriptomic and regional identities. Using SEEP, we analyze spheroid, organoid, and in vivo tumor models of high-grade serous ovarian cancer (HGSOC). The results validate long-standing beliefs about the relationship between cell state and position while revealing new concepts regarding how spatially unique microenvironments influence the identity of individual cells within tumors.
    MeSH term(s) Transcriptome/genetics ; Gene Expression Profiling ; Kinetics ; Organoids ; Physics
    Language English
    Publishing date 2023-06-22
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2854138-8
    ISSN 2405-4720 ; 2405-4712
    ISSN (online) 2405-4720
    ISSN 2405-4712
    DOI 10.1016/j.cels.2023.05.003
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: Author Correction: Massively parallel single-cell mitochondrial DNA genotyping and chromatin profiling.

    Lareau, Caleb A / Ludwig, Leif S / Muus, Christoph / Gohil, Satyen H / Zhao, Tongtong / Chiang, Zachary / Pelka, Karin / Verboon, Jeffrey M / Luo, Wendy / Christian, Elena / Rosebrock, Daniel / Getz, Gad / Boland, Genevieve M / Chen, Fei / Buenrostro, Jason D / Hacohen, Nir / Wu, Catherine J / Aryee, Martin J / Regev, Aviv /
    Sankaran, Vijay G

    Nature biotechnology

    2023  Volume 41, Issue 9, Page(s) 1345

    Language English
    Publishing date 2023-08-31
    Publishing country United States
    Document type Published Erratum
    ZDB-ID 1311932-1
    ISSN 1546-1696 ; 1087-0156
    ISSN (online) 1546-1696
    ISSN 1087-0156
    DOI 10.1038/s41587-023-01942-1
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article: A deep lung cell atlas reveals cytokine-mediated lineage switching of a rare cell progenitor of the human airway epithelium.

    Waghray, Avinash / Monga, Isha / Lin, Brian / Shah, Viral / Slyper, Michal / Giotti, Bruno / Xu, Jiajie / Waldman, Julia / Dionne, Danielle / Nguyen, Lan T / Lou, Wendy / Cai, Peiwen / Park, Eric / Muus, Christoph / Sun, Jiawei / Surve, Manalee V / Yang, Lujia Cha Cha / Rozenblatt-Rosen, Orit / Dolerey, Toni M /
    Saladi, Srinivas Vinod / Tsankov, Alexander M / Regev, Aviv / Rajagopal, Jayaraj

    bioRxiv : the preprint server for biology

    2023  

    Abstract: The human airway contains specialized rare epithelial cells whose roles in respiratory disease are not well understood. Ionocytes express the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR), while chemosensory tuft cells express asthma- ... ...

    Abstract The human airway contains specialized rare epithelial cells whose roles in respiratory disease are not well understood. Ionocytes express the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR), while chemosensory tuft cells express asthma-associated alarmins. However, surprisingly, exceedingly few mature tuft cells have been identified in human lung cell atlases despite the ready identification of rare ionocytes and neuroendocrine cells. To identify human rare cell progenitors and define their lineage relationship to mature tuft cells, we generated a deep lung cell atlas containing 311,748 single cell RNA-Seq (scRNA-seq) profiles from discrete anatomic sites along the large and small airways and lung lobes of explanted donor lungs that could not be used for organ transplantation. Of 154,222 airway epithelial cells, we identified 687 ionocytes (0.45%) that are present in similar proportions in both large and small airways, suggesting that they may contribute to both large and small airways pathologies in CF. In stark contrast, we recovered only 3 mature tuft cells (0.002%). Instead, we identified rare bipotent progenitor cells that can give rise to both ionocytes and tuft cells, which we termed tuft-ionocyte progenitor cells (TIP cells). Remarkably, the cycling fraction of these TIP cells was comparable to that of basal stem cells. We used scRNA-seq and scATAC-seq to predict transcription factors that mark this novel rare cell progenitor population and define intermediate states during TIP cell lineage transitions en route to the differentiation of mature ionocytes and tuft cells. The default lineage of TIP cell descendants is skewed towards ionocytes, explaining the paucity of mature tuft cells in the human airway. However, Type 2 and Type 17 cytokines, associated with asthma and CF, diverted the lineage of TIP cell descendants
    Language English
    Publishing date 2023-11-29
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2023.11.28.569028
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article: Myocyte Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2 mediated myocarditis.

    Tucker, Nathan R / Chaffin, Mark / Bedi, Kenneth C / Papangeli, Irinna / Akkad, Amer-Denis / Arduini, Alessandro / Hayat, Sikander / Eraslan, Gökcen / Muus, Christoph / Bhattacharyya, Roby / Stegmann, Christian M / Margulies, Kenneth B / Ellinor, Patrick T

    medRxiv : the preprint server for health sciences

    2020  

    Abstract: Coronavirus disease 2019 (COVID-19) is a global pandemic caused by a novel severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). SARS-CoV-2 infection of host cells occurs predominantly via binding of the viral surface spike protein to the human ... ...

    Abstract Coronavirus disease 2019 (COVID-19) is a global pandemic caused by a novel severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2). SARS-CoV-2 infection of host cells occurs predominantly via binding of the viral surface spike protein to the human angiotensin-converting enzyme 2 (ACE2) receptor. Hypertension and pre-existing cardiovascular disease are risk factors for morbidity from COVID-19, and it remains uncertain whether the use of angiotensin converting enzyme inhibitors (ACEi) or angiotensin receptor blockers (ARB) impacts infection and disease. Here, we aim to shed light on this question by assessing ACE2 expression in normal and diseased human myocardial samples profiled by bulk and single nucleus RNA-seq.
    Keywords covid19
    Language English
    Publishing date 2020-04-14
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2020.04.09.20059204
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: Myocyte-Specific Upregulation of

    Tucker, Nathan R / Chaffin, Mark / Bedi, Kenneth C / Papangeli, Irinna / Akkad, Amer-Denis / Arduini, Alessandro / Hayat, Sikander / Eraslan, Gökcen / Muus, Christoph / Bhattacharyya, Roby P / Stegmann, Christian M / Margulies, Kenneth B / Ellinor, Patrick T

    Circulation

    2020  Volume 142, Issue 7, Page(s) 708–710

    MeSH term(s) Angiotensin-Converting Enzyme 2 ; Betacoronavirus/isolation & purification ; Betacoronavirus/pathogenicity ; COVID-19 ; Cardiomyopathy, Dilated/genetics ; Cardiomyopathy, Dilated/pathology ; Cardiomyopathy, Hypertrophic/genetics ; Cardiomyopathy, Hypertrophic/pathology ; Cathepsin L/genetics ; Cathepsin L/metabolism ; Coronavirus Infections/complications ; Coronavirus Infections/pathology ; Coronavirus Infections/virology ; Heart Ventricles/metabolism ; Humans ; Myocarditis/diagnosis ; Myocarditis/etiology ; Myocardium/metabolism ; Pandemics ; Peptidyl-Dipeptidase A/chemistry ; Peptidyl-Dipeptidase A/genetics ; Peptidyl-Dipeptidase A/metabolism ; Pneumonia, Viral/complications ; Pneumonia, Viral/pathology ; Pneumonia, Viral/virology ; Protease Inhibitors/pharmacology ; RNA-Seq ; SARS-CoV-2 ; Serine Endopeptidases/genetics ; Serine Endopeptidases/metabolism ; Up-Regulation/drug effects
    Chemical Substances Protease Inhibitors ; Peptidyl-Dipeptidase A (EC 3.4.15.1) ; ACE2 protein, human (EC 3.4.17.23) ; Angiotensin-Converting Enzyme 2 (EC 3.4.17.23) ; Serine Endopeptidases (EC 3.4.21.-) ; TMPRSS2 protein, human (EC 3.4.21.-) ; CTSL protein, human (EC 3.4.22.15) ; Cathepsin L (EC 3.4.22.15)
    Keywords covid19
    Language English
    Publishing date 2020-06-22
    Publishing country United States
    Document type Letter ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 80099-5
    ISSN 1524-4539 ; 0009-7322 ; 0069-4193 ; 0065-8499
    ISSN (online) 1524-4539
    ISSN 0009-7322 ; 0069-4193 ; 0065-8499
    DOI 10.1161/CIRCULATIONAHA.120.047911
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Single-cell multi-omics of mitochondrial DNA disorders reveals dynamics of purifying selection across human immune cells.

    Lareau, Caleb A / Dubois, Sonia M / Buquicchio, Frank A / Hsieh, Yu-Hsin / Garg, Kopal / Kautz, Pauline / Nitsch, Lena / Praktiknjo, Samantha D / Maschmeyer, Patrick / Verboon, Jeffrey M / Gutierrez, Jacob C / Yin, Yajie / Fiskin, Evgenij / Luo, Wendy / Mimitou, Eleni P / Muus, Christoph / Malhotra, Rhea / Parikh, Sumit / Fleming, Mark D /
    Oevermann, Lena / Schulte, Johannes / Eckert, Cornelia / Kundaje, Anshul / Smibert, Peter / Vardhana, Santosha A / Satpathy, Ansuman T / Regev, Aviv / Sankaran, Vijay G / Agarwal, Suneet / Ludwig, Leif S

    Nature genetics

    2023  Volume 55, Issue 7, Page(s) 1198–1209

    Abstract: Pathogenic mutations in mitochondrial DNA (mtDNA) compromise cellular metabolism, contributing to cellular heterogeneity and disease. Diverse mutations are associated with diverse clinical phenotypes, suggesting distinct organ- and cell-type-specific ... ...

    Abstract Pathogenic mutations in mitochondrial DNA (mtDNA) compromise cellular metabolism, contributing to cellular heterogeneity and disease. Diverse mutations are associated with diverse clinical phenotypes, suggesting distinct organ- and cell-type-specific metabolic vulnerabilities. Here we establish a multi-omics approach to quantify deletions in mtDNA alongside cell state features in single cells derived from six patients across the phenotypic spectrum of single large-scale mtDNA deletions (SLSMDs). By profiling 206,663 cells, we reveal the dynamics of pathogenic mtDNA deletion heteroplasmy consistent with purifying selection and distinct metabolic vulnerabilities across T-cell states in vivo and validate these observations in vitro. By extending analyses to hematopoietic and erythroid progenitors, we reveal mtDNA dynamics and cell-type-specific gene regulatory adaptations, demonstrating the context-dependence of perturbing mitochondrial genomic integrity. Collectively, we report pathogenic mtDNA heteroplasmy dynamics of individual blood and immune cells across lineages, demonstrating the power of single-cell multi-omics for revealing fundamental properties of mitochondrial genetics.
    MeSH term(s) Humans ; DNA, Mitochondrial/genetics ; Multiomics ; Mitochondrial Diseases/genetics ; Mitochondria/genetics ; Mutation
    Chemical Substances DNA, Mitochondrial
    Language English
    Publishing date 2023-06-29
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 1108734-1
    ISSN 1546-1718 ; 1061-4036
    ISSN (online) 1546-1718
    ISSN 1061-4036
    DOI 10.1038/s41588-023-01433-8
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Phase II trials of zilucoplan in paroxysmal nocturnal hemoglobinuria.

    Kulasekararaj, Austin G / Lehtinen, Anna-Elina / Forsyth, Cecily / Gandhi, Shreyans / Griffin, Morag / Körper, Sixten / Mikala, Gabor / Muus, Petra / Overgaard, Ulrik / Patriquin, Christopher J / Pullon, Humphrey / Shen, Yu-Min / Spearing, Ruth / Szer, Jeff / De la Borderie, Guillemette / Duda, Petra W / Farzaneh-Far, Ramin / Ragunathan, Sharan / Sayegh, Camil E /
    Vadysirisack, Douangsone D / Schrezenmeier, Hubert

    Haematologica

    2024  Volume 109, Issue 3, Page(s) 929–935

    MeSH term(s) Humans ; Complement C5/therapeutic use ; Hemoglobinuria, Paroxysmal/drug therapy ; Peptides, Cyclic/therapeutic use
    Chemical Substances Complement C5 ; Peptides, Cyclic ; zilucoplan (YG391PK0CC)
    Language English
    Publishing date 2024-03-01
    Publishing country Italy
    Document type Clinical Trial, Phase II ; Letter
    ZDB-ID 2333-4
    ISSN 1592-8721 ; 0017-6567 ; 0390-6078
    ISSN (online) 1592-8721
    ISSN 0017-6567 ; 0390-6078
    DOI 10.3324/haematol.2022.281780
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Transcriptional States and Chromatin Accessibility Underlying Human Erythropoiesis.

    Ludwig, Leif S / Lareau, Caleb A / Bao, Erik L / Nandakumar, Satish K / Muus, Christoph / Ulirsch, Jacob C / Chowdhary, Kaitavjeet / Buenrostro, Jason D / Mohandas, Narla / An, Xiuli / Aryee, Martin J / Regev, Aviv / Sankaran, Vijay G

    Cell reports

    2019  Volume 27, Issue 11, Page(s) 3228–3240.e7

    Abstract: Human erythropoiesis serves as a paradigm of physiologic cellular differentiation. This process is also of considerable interest for better understanding anemias and identifying new therapies. Here, we apply deep transcriptomic and accessible chromatin ... ...

    Abstract Human erythropoiesis serves as a paradigm of physiologic cellular differentiation. This process is also of considerable interest for better understanding anemias and identifying new therapies. Here, we apply deep transcriptomic and accessible chromatin profiling to characterize a faithful ex vivo human erythroid differentiation system from hematopoietic stem and progenitor cells. We reveal stage-specific transcriptional states and chromatin accessibility during various stages of erythropoiesis, including 14,260 differentially expressed genes and 63,659 variably accessible chromatin peaks. Our analysis suggests differentiation stage-predominant roles for specific master regulators, including GATA1 and KLF1. We integrate chromatin profiles with common and rare genetic variants associated with erythroid cell traits and diseases, finding that variants regulating different erythroid phenotypes likely act at variable points during differentiation. In addition, we identify a regulator of terminal erythropoiesis, TMCC2, more broadly illustrating the value of this comprehensive analysis to improve our understanding of erythropoiesis in health and disease.
    MeSH term(s) Aged ; Cells, Cultured ; Chromatin/chemistry ; Chromatin/metabolism ; Chromatin Assembly and Disassembly ; Erythroid Precursor Cells/cytology ; Erythroid Precursor Cells/metabolism ; Erythropoiesis ; Female ; GATA1 Transcription Factor/genetics ; GATA1 Transcription Factor/metabolism ; HEK293 Cells ; Humans ; Kruppel-Like Transcription Factors/genetics ; Kruppel-Like Transcription Factors/metabolism ; Membrane Proteins/genetics ; Membrane Proteins/metabolism ; Middle Aged ; Polymorphism, Single Nucleotide ; Transcriptome
    Chemical Substances Chromatin ; GATA1 Transcription Factor ; GATA1 protein, human ; Kruppel-Like Transcription Factors ; Membrane Proteins ; TMCC2 protein, human ; erythroid Kruppel-like factor
    Language English
    Publishing date 2019-07-09
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2649101-1
    ISSN 2211-1247 ; 2211-1247
    ISSN (online) 2211-1247
    ISSN 2211-1247
    DOI 10.1016/j.celrep.2019.05.046
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  10. Article: Myocyte-Specific Upregulation of ACE2 in Cardiovascular Disease: Implications for SARS-CoV-2-Mediated Myocarditis

    Tucker, Nathan R / Chaffin, Mark / Bedi, Kenneth C / Papangeli, Irinna / Akkad, Amer-Denis / Arduini, Alessandro / Hayat, Sikander / Eraslan, Gökcen / Muus, Christoph / Bhattacharyya, Roby P / Stegmann, Christian M / Margulies, Kenneth B / Ellinor, Patrick T

    Circulation

    Keywords covid19
    Publisher WHO
    Document type Article
    Note WHO #Covidence: #717429
    Database COVID19

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