A cellular and spatial map of the choroid plexus across brain ventricles and ages
暂无分享,去创建一个
Maria K. Lehtinen | Frederick B. Shipley | A. Regev | Naomi Habib | C. Rodman | O. Rozenblatt-Rosen | Danielle Dionne | Samantha J. Riesenfeld | Rebecca H. Herbst | Lan Nguyen | Feng Zhang | R. Sedláček | V. Bryja | M. Procházková | J. Procházka | Neil Dani | Jin Cui | Joshua P. Head | Ahram Jang | C. McCabe | G. Green | Karol Kaiser | N. Habib | Christopher Rodman
[1] Monika S. Kowalczyk,et al. Skin-resident innate lymphoid cells converge on a pathogenic effector state , 2021, Nature.
[2] Maria K. Lehtinen,et al. Choroid plexus NKCC1 mediates cerebrospinal fluid clearance during mouse early postnatal development , 2021, Nature Communications.
[3] I. Cobos,et al. Broad transcriptional dysregulation of brain and choroid plexus cell types with COVID-19 , 2020, bioRxiv.
[4] A. Helenius,et al. Neuropilin-1 facilitates SARS-CoV-2 cell entry and infectivity , 2020, Science.
[5] Madeline A. Lancaster,et al. SARS-CoV-2 Infects the Brain Choroid Plexus and Disrupts the Blood-CSF Barrier in Human Brain Organoids , 2020, Cell Stem Cell.
[6] Maria K. Lehtinen,et al. Inflammation of the Embryonic Choroid Plexus Barrier following Maternal Immune Activation. , 2020, Developmental cell.
[7] Kenneth L. Jones,et al. Single-Cell Transcriptomic Analyses of the Developing Meninges Reveal Meningeal Fibroblast Diversity and Function. , 2020, Developmental cell.
[8] Christoph Bock,et al. Structural cells are key regulators of organ-specific immune response , 2020, Nature.
[9] Madeline A. Lancaster,et al. Human CNS barrier-forming organoids with cerebrospinal fluid production , 2020, Science.
[10] J. Sejvar,et al. Neurological associations of COVID-19 , 2020, The Lancet Neurology.
[11] David S. Fischer,et al. Integrated analyses of single-cell atlases reveal age, gender, and smoking status associations with cell type-specific expression of mediators of SARS-CoV-2 viral entry and highlights inflammatory programs in putative target cells , 2020, bioRxiv.
[12] K. Hashimoto,et al. Nervous system involvement after infection with COVID-19 and other coronaviruses , 2020, Brain, Behavior, and Immunity.
[13] Maria K. Lehtinen,et al. Tracking Calcium Dynamics and Immune Surveillance at the Choroid Plexus Blood-Cerebrospinal Fluid Interface , 2020, Neuron.
[14] Mirjana Efremova,et al. CellPhoneDB: inferring cell–cell communication from combined expression of multi-subunit ligand–receptor complexes , 2020, Nature Protocols.
[15] Maria K. Lehtinen,et al. Emergence and Developmental Roles of the Cerebrospinal Fluid System. , 2020, Developmental cell.
[16] John C. Marioni,et al. Unsupervised removal of systematic background noise from droplet-based single-cell experiments using CellBender , 2019, bioRxiv.
[17] Yvan Saeys,et al. A single-cell atlas of mouse brain macrophages reveals unique transcriptional identities shaped by ontogeny and tissue environment , 2019, Nature Neuroscience.
[18] R. Barker,et al. WNT5A is transported via lipoprotein particles in the cerebrospinal fluid to regulate hindbrain morphogenesis , 2019, Nature Communications.
[19] P. Rigollet,et al. Optimal-Transport Analysis of Single-Cell Gene Expression Identifies Developmental Trajectories in Reprogramming , 2019, Cell.
[20] Tuan Leng Tay,et al. Single-cell profiling identifies myeloid cell subsets with distinct fates during neuroinflammation , 2019, Science.
[21] P. Sims,et al. Single-Cell Analysis of Regional Differences in Adult V-SVZ Neural Stem Cell Lineages , 2019, Cell reports.
[22] Evan Z. Macosko,et al. Single‐Cell RNA Sequencing of Microglia throughout the Mouse Lifespan and in the Injured Brain Reveals Complex Cell‐State Changes , 2019, Immunity.
[23] Lai Guan Ng,et al. Dimensionality reduction for visualizing single-cell data using UMAP , 2018, Nature Biotechnology.
[24] Bo Li,et al. Nuclei multiplexing with barcoded antibodies for single-nucleus genomics , 2018, Nature Communications.
[25] Monika S. Kowalczyk,et al. Skin inflammation driven by differentiation of quiescent tissue-resident ILCs into a spectrum of pathogenic effectors , 2018, bioRxiv.
[26] L. Mucke,et al. Klotho controls the brain–immune system interface in the choroid plexus , 2018, Proceedings of the National Academy of Sciences.
[27] I. Amit,et al. Lung Single-Cell Signaling Interaction Map Reveals Basophil Role in Macrophage Imprinting , 2018, Cell.
[28] N. Neff,et al. Developmental Heterogeneity of Microglia and Brain Myeloid Cells Revealed by Deep Single-Cell RNA Sequencing , 2018, Neuron.
[29] Aviv Regev,et al. A revised airway epithelial hierarchy includes CFTR-expressing ionocytes , 2018, Nature.
[30] Evan Z. Macosko,et al. Molecular Diversity and Specializations among the Cells of the Adult Mouse Brain , 2018, Cell.
[31] Jun Kit Wang,et al. Hyaluronan Receptor LYVE‐1‐Expressing Macrophages Maintain Arterial Tone through Hyaluronan‐Mediated Regulation of Smooth Muscle Cell Collagen , 2018, Immunity.
[32] Erik Sundström,et al. RNA velocity of single cells , 2018, Nature.
[33] N. Saunders,et al. Physiology and molecular biology of barrier mechanisms in the fetal and neonatal brain , 2018, The Journal of physiology.
[34] Maria K. Lehtinen,et al. The ESCRT-III Protein CHMP1A Mediates Secretion of Sonic Hedgehog on a Distinctive Subtype of Extracellular Vesicles , 2018, Cell reports.
[35] Zev J. Gartner,et al. DoubletFinder: Doublet detection in single-cell RNA sequencing data using artificial nearest neighbors , 2018, bioRxiv.
[36] Patrick J. Whelan,et al. Single-Cell Transcriptomics and Fate Mapping of Ependymal Cells Reveals an Absence of Neural Stem Cell Function , 2018, Cell.
[37] Paul Hoffman,et al. Integrating single-cell transcriptomic data across different conditions, technologies, and species , 2018, Nature Biotechnology.
[38] Maria K. Lehtinen,et al. Mice Expressing Myc in Neural Precursors Develop Choroid Plexus and Ciliary Body Tumors. , 2018, The American journal of pathology.
[39] Hanspeter Herzel,et al. The choroid plexus is an important circadian clock component , 2018, Nature Communications.
[40] Koji Ando,et al. A molecular atlas of cell types and zonation in the brain vasculature , 2018, Nature.
[41] Leland McInnes,et al. UMAP: Uniform Manifold Approximation and Projection for Dimension Reduction , 2018, ArXiv.
[42] J. Ghersi-Egea,et al. Molecular anatomy and functions of the choroidal blood-cerebrospinal fluid barrier in health and disease , 2018, Acta Neuropathologica.
[43] A. Fournier,et al. IL-1β enables CNS access to CCR2hi monocytes and the generation of pathogenic cells through GM-CSF released by CNS endothelial cells , 2018, Proceedings of the National Academy of Sciences.
[44] M. Bronner,et al. Regulatory Logic Underlying Diversification of the Neural Crest. , 2017, Trends in genetics : TIG.
[45] A. van Oudenaarden,et al. Single-cell sequencing reveals dissociation-induced gene expression in tissue subpopulations , 2017, Nature Methods.
[46] Aviv Regev,et al. Massively-parallel single nucleus RNA-seq with DroNc-seq , 2017, Nature Methods.
[47] Guido Gerig,et al. Increased Extra-axial Cerebrospinal Fluid in High-Risk Infants Who Later Develop Autism , 2017, Biological Psychiatry.
[48] J. Simard,et al. Inflammation-dependent cerebrospinal fluid hypersecretion by the choroid plexus epithelium in posthemorrhagic hydrocephalus , 2017, Nature Medicine.
[49] A. Brunet,et al. Single-Cell Transcriptomic Analysis Defines Heterogeneity and Transcriptional Dynamics in the Adult Neural Stem Cell Lineage. , 2017, Cell reports.
[50] V. Silva-Vargas,et al. Age-Dependent Niche Signals from the Choroid Plexus Regulate Adult Neural Stem Cells. , 2016, Cell stem cell.
[51] Aviv Regev,et al. A Distinct Gene Module for Dysfunction Uncoupled from Activation in Tumor-Infiltrating T Cells , 2016, Cell.
[52] Maria K. Lehtinen,et al. Comment on “Multiple repressive mechanisms in the hippocampus during memory formation” , 2016, Science.
[53] Melissa Weintraub. The line between science and politics , 2016, Science.
[54] G. Eichele,et al. Cilia-based flow network in the brain ventricles , 2016, Science.
[55] Matthew Stephens,et al. Visualizing the structure of RNA-seq expression data using grade of membership models , 2016, bioRxiv.
[56] Sara B. Linker,et al. Nuclear RNA-seq of single neurons reveals molecular signatures of activation , 2016, Nature Communications.
[57] R. Vandenbroucke,et al. The choroid plexus-cerebrospinal fluid interface in Alzheimer's disease: more than just a barrier , 2016, Neural regeneration research.
[58] Fabian J Theis,et al. Diffusion pseudotime robustly reconstructs lineage branching , 2016, Nature Methods.
[59] A. Kania,et al. Mechanisms of ephrin–Eph signalling in development, physiology and disease , 2016, Nature Reviews Molecular Cell Biology.
[60] P. Linsley,et al. MAST: a flexible statistical framework for assessing transcriptional changes and characterizing heterogeneity in single-cell RNA sequencing data , 2015, Genome Biology.
[61] Lixia Li,et al. The regulation of immune cell trafficking by the extracellular matrix. , 2015, Current opinion in cell biology.
[62] Fabian J. Theis,et al. Diffusion maps for high-dimensional single-cell analysis of differentiation data , 2015, Bioinform..
[63] Fabian J. Theis,et al. destiny: diffusion maps for large-scale single-cell data in R , 2015, Bioinform..
[64] Maria K. Lehtinen,et al. Development and functions of the choroid plexus–cerebrospinal fluid system , 2015, Nature Reviews Neuroscience.
[65] Enza Torino,et al. Head and Neck Veins of the Mouse. A Magnetic Resonance, Micro Computed Tomography and High Frequency Color Doppler Ultrasound Study , 2015, PloS one.
[66] D. Ellison,et al. Cross-Species Genomics Identifies TAF12, NFYC, and RAD54L as Choroid Plexus Carcinoma Oncogenes. , 2015, Cancer cell.
[67] Maria K. Lehtinen,et al. Zebrafish cerebrospinal fluid mediates cell survival through a retinoid signaling pathway , 2015, Developmental neurobiology.
[68] Maria K. Lehtinen,et al. Spatially Heterogeneous Choroid Plexus Transcriptomes Encode Positional Identity and Contribute to Regional CSF Production , 2015, The Journal of Neuroscience.
[69] Eugene J. Barrett,et al. Insulin Regulates Brain Function, but How Does It Get There? , 2014, Diabetes.
[70] J. Wallingford,et al. Multiciliated Cells , 2014, Current Biology.
[71] I. Amit,et al. Aging-induced type I interferon response at the choroid plexus negatively affects brain function , 2014, Science.
[72] S. Butz,et al. Esm1 Modulates Endothelial Tip Cell Behavior and Vascular Permeability by Enhancing VEGF Bioavailability , 2014, Circulation research.
[73] P. Bonaldo,et al. Extracellular matrix: A dynamic microenvironment for stem cell niche , 2014, Biochimica et biophysica acta.
[74] Dong Liu,et al. Functional roles of Lgr4 and Lgr5 in embryonic gut, kidney and skin development in mice. , 2014, Developmental biology.
[75] C. Kahn,et al. Insulin Action in Brain Regulates Systemic Metabolism and Brain Function , 2014, Diabetes.
[76] Yoav Mayshar,et al. Mfsd2a is critical for the formation and function of the blood–brain barrier , 2014, Nature.
[77] Ansuman T. Satpathy,et al. Heme-Mediated SPI-C Induction Promotes Monocyte Differentiation into Iron-Recycling Macrophages , 2014, Cell.
[78] M. Schwartz,et al. The resolution of neuroinflammation in neurodegeneration: leukocyte recruitment via the choroid plexus , 2014, The EMBO journal.
[79] N. Sousa,et al. Blood–brain-barriers in aging and in Alzheimer’s disease , 2013, Molecular Neurodegeneration.
[80] J. Praetorius,et al. Cerebrospinal fluid secretion by the choroid plexus. , 2013, Physiological reviews.
[81] Philippe Soriano,et al. The widely used Wnt1-Cre transgene causes developmental phenotypes by ectopic activation of Wnt signaling. , 2013, Developmental biology.
[82] D. Amaral,et al. Early brain enlargement and elevated extra-axial fluid in infants who develop autism spectrum disorder. , 2013, Brain : a journal of neurology.
[83] P. Low,et al. Choroid plexus transcytosis and exosome shuttling deliver folate into brain parenchyma , 2013, Nature Communications.
[84] Steffen Jung,et al. Recruitment of beneficial M2 macrophages to injured spinal cord is orchestrated by remote brain choroid plexus. , 2013, Immunity.
[85] N. Sousa,et al. Do genes and environment meet to regulate cerebrospinal fluid dynamics? Relevance for schizophrenia , 2012, Front. Cell. Neurosci..
[86] E. Tamm,et al. Lack of endothelial diaphragms in fenestrae and caveolae of mutant Plvap-deficient mice , 2012, Histochemistry and Cell Biology.
[87] M. Zervas,et al. Wnt1 expression temporally allocates upper rhombic lip progenitors and defines their terminal cell fate in the cerebellum , 2012, Molecular and Cellular Neuroscience.
[88] Maria K. Lehtinen,et al. The Cerebrospinal Fluid Provides a Proliferative Niche for Neural Progenitor Cells , 2011, Neuron.
[89] S. Liddelow,et al. Development of the lateral ventricular choroid plexus in a marsupial, Monodelphis domestica , 2010, Cerebrospinal Fluid Research.
[90] Hans Clevers,et al. Intestinal Crypt Homeostasis Results from Neutral Competition between Symmetrically Dividing Lgr5 Stem Cells , 2010, Cell.
[91] D. McKean,et al. The iron exporter ferroportin 1 is essential for development of the mouse embryo, forebrain patterning and neural tube closure , 2010, Development.
[92] M. K. Cooper,et al. Transventricular delivery of Sonic hedgehog is essential to cerebellar ventricular zone development , 2010, Proceedings of the National Academy of Sciences.
[93] S. Dymecki,et al. Sonic hedgehog is required for vascular outgrowth in the hindbrain choroid plexus. , 2010, Developmental biology.
[94] S. Dey,et al. Sonic hedgehog signaling regulates a novel epithelial progenitor domain of the hindbrain choroid plexus , 2009, Development.
[95] Arnold Kriegstein,et al. The glial nature of embryonic and adult neural stem cells. , 2009, Annual review of neuroscience.
[96] B. Engelhardt,et al. C-C chemokine receptor 6–regulated entry of TH-17 cells into the CNS through the choroid plexus is required for the initiation of EAE , 2009, Nature Immunology.
[97] Israel Steinfeld,et al. BMC Bioinformatics BioMed Central , 2008 .
[98] K. Murphy,et al. Critical role for Spi-C in the development of red pulp macrophages and splenic iron homeostasis , 2008, Nature.
[99] J. Whitsett,et al. R-spondin 2 is required for normal laryngeal-tracheal, lung and limb morphogenesis , 2008, Development.
[100] R. W. Draft,et al. Transgenic strategies for combinatorial expression of fluorescent proteins in the nervous system , 2007, Nature.
[101] S. Dymecki,et al. Molecularly and temporally separable lineages form the hindbrain roof plate and contribute differentially to the choroid plexus , 2007, Development.
[102] Zohar Yakhini,et al. Discovering Motifs in Ranked Lists of DNA Sequences , 2007, PLoS Comput. Biol..
[103] Allan R. Jones,et al. Genome-wide atlas of gene expression in the adult mouse brain , 2007, Nature.
[104] Hideyuki Okano,et al. New Neurons Follow the Flow of Cerebrospinal Fluid in the Adult Brain , 2006, Science.
[105] J Fernando Bazan,et al. IL-33, an interleukin-1-like cytokine that signals via the IL-1 receptor-related protein ST2 and induces T helper type 2-associated cytokines. , 2005, Immunity.
[106] A. Donovan,et al. The iron exporter ferroportin/Slc40a1 is essential for iron homeostasis. , 2005, Cell metabolism.
[107] Luis Puelles,et al. Forebrain gene expression domains and the evolving prosomeric model , 2003, Trends in Neurosciences.
[108] Philippe Soriano,et al. Cryptic boundaries in roof plate and choroid plexus identified by intersectional gene activation , 2003, Nature Genetics.
[109] C. Rahner,et al. Claudin 5 Is Transiently Expressed During the Development of the Retinal Pigment Epithelium , 2002, The Journal of Membrane Biology.
[110] Christopher C W Hughes,et al. Identification of endothelial cell genes expressed in an in vitro model of angiogenesis: induction of ESM-1, (beta)ig-h3, and NrCAM. , 2002, Microvascular research.
[111] Marcus Fruttiger,et al. Development of the mouse retinal vasculature: angiogenesis versus vasculogenesis. , 2002, Investigative ophthalmology & visual science.
[112] M E J Newman,et al. Community structure in social and biological networks , 2001, Proceedings of the National Academy of Sciences of the United States of America.
[113] R. Wingate,et al. The rhombic lip and early cerebellar development , 2001, Current Opinion in Neurobiology.
[114] Michael I. Jordan,et al. Latent Dirichlet Allocation , 2001, J. Mach. Learn. Res..
[115] M. Wassef,et al. Ectopic engrailed 1 expression in the dorsal midline causes cell death, abnormal differentiation of circumventricular organs and errors in axonal pathfinding. , 2000, Development.
[116] P. Donnelly,et al. Inference of population structure using multilocus genotype data. , 2000, Genetics.
[117] G. Palade,et al. PV-1 is a component of the fenestral and stomatal diaphragms in fenestrated endothelia. , 1999, Proceedings of the National Academy of Sciences of the United States of America.
[118] Pao-Tien Chuang,et al. Vertebrate Hedgehog signalling modulated by induction of a Hedgehog-binding protein , 1999, Nature.
[119] Tadashi Kaname,et al. Mutation of the mouse klotho gene leads to a syndrome resembling ageing , 1997, Nature.
[120] R. Keep,et al. A morphometric study on the development of the lateral ventricle choroid plexus, choroid plexus capillaries and ventricular ependyma in the rat. , 1990, Brain research. Developmental brain research.
[121] B. Christ,et al. An experimental and ultrastructural study on the development of the avian choroid plexus , 1989, Cell and Tissue Research.
[122] S. Woods,et al. Immunocytochemical detection of insulin in rat hypothalamus and its possible uptake from cerebrospinal fluid. , 1983, Endocrinology.
[123] B. Posner,et al. Insulin-binding sites in the rat brain: in vivo localization to the circumventricular organs by quantitative radioautography. , 1979, Endocrinology.
[124] M. Moskowitz,et al. Raphe origin of serotonin-containing neurons within choroid plexus of the rat , 1979, Brain Research.
[125] L. Edvinsson,et al. Sympathetic nervous control of cerebrospinal fluid production from the choroid plexus. , 1978, Science.
[126] A. Hudson. The development of the vascular pattern of the choroid plexus of the lateral ventricles , 1960, The Journal of comparative neurology.
[127] Qing-Rong Liu,et al. Insulin is produced in choroid plexus and its release is regulated by serotonergic signaling , 2019 .
[128] Charlotte N. Henrichsen,et al. Explorer A High-Resolution Anatomical Atlas of the Transcriptome in the Mouse Embryo , 2016 .
[129] J. Flanagan,et al. RNAscope: a novel in situ RNA analysis platform for formalin-fixed, paraffin-embedded tissues. , 2012, The Journal of molecular diagnostics : JMD.
[130] Geoffrey E. Hinton,et al. Visualizing Data using t-SNE , 2008 .
[131] Gregor Eichele,et al. GenePaint.org: an atlas of gene expression patterns in the mouse embryo , 2004, Nucleic Acids Res..
[132] M. Netsky,et al. Histogenesis of choroid plexus in man. , 1966, The American journal of anatomy.
[133] Andrew E. Jaffe,et al. Bioinformatics Applications Note Gene Expression the Sva Package for Removing Batch Effects and Other Unwanted Variation in High-throughput Experiments , 2022 .