Spatial reconstruction of single enterocytes uncovers broad zonation along the intestinal villus axis

The intestinal epithelium is a highly structured tissue composed of repeating crypt-villus units1,2. Enterocytes, which constitute the most abundant cell type, perform the diverse tasks of absorbing a wide range of nutrients while protecting the body from the harsh bacterial-rich environment. It is unknown if these tasks are equally performed by all enterocytes or whether they are spatially zonated along the villus axis3. Here, we performed whole-transcriptome measurements of laser-capture-microdissected villus segments to extract a large panel of landmark genes, expressed in a zonated manner. We used these genes to localize single sequenced enterocytes along the villus axis, thus reconstructing a global spatial expression map. We found that most enterocyte genes were zonated. Enterocytes at villi bottoms expressed an anti-bacterial Reg gene program in a microbiome-dependent manner, potentially reducing the crypt pathogen exposure. Translation, splicing and respiration genes steadily decreased in expression towards the villi tops, whereas distinct mid-top villus zones sub-specialized in the absorption of carbohydrates, peptides and fat. Enterocytes at the villi tips exhibited a unique gene-expression signature consisting of Klf4, Egfr, Neat1, Malat1, cell adhesion and purine metabolism genes. Our study exposes broad spatial heterogeneity of enterocytes, which could be important for achieving their diverse tasks.

[1]  K. Takeda,et al.  Lypd8 promotes the segregation of flagellated microbiota and colonic epithelia , 2016, Nature.

[2]  J. Nicholson,et al.  Metabolome, transcriptome, and bioinformatic cis-element analyses point to HNF-4 as a central regulator of gene expression during enterocyte differentiation. , 2006, Physiological genomics.

[3]  J. Sévigny,et al.  The E-NTPDase family of ectonucleotidases: Structure function relationships and pathophysiological significance , 2006, Purinergic Signalling.

[4]  A. Oudenaarden,et al.  Single-molecule transcript counting of stem-cell markers in the mouse intestine , 2011, Nature Cell Biology.

[5]  Yarden Katz,et al.  A single-cell survey of the small intestinal epithelium , 2017, Nature.

[6]  Lior Pachter,et al.  Differential analysis of RNA-seq incorporating quantification uncertainty , 2016, Nature Methods.

[7]  Cesare Furlanello,et al.  A promoter-level mammalian expression atlas , 2015 .

[8]  S. Itzkovitz,et al.  Global mRNA polarization regulates translation efficiency in the intestinal epithelium , 2017, Science.

[9]  J. Bertrand-Michel,et al.  Lipidomic and Spatio-Temporal Imaging of Fat by Mass Spectrometry in Mice Duodenum during Lipid Digestion , 2013, PloS one.

[10]  A. Oudenaarden,et al.  Single-molecule mRNA detection and counting in mammalian tissue , 2013, Nature Protocols.

[11]  E. Kunkel,et al.  The Intestinal Chemokine Thymus-expressed Chemokine (CCL25) Attracts IgA Antibody-secreting Cells , 2002, The Journal of experimental medicine.

[12]  S. Colgan,et al.  Physiologic hypoxia and oxygen homeostasis in the healthy intestine. A Review in the Theme: Cellular Responses to Hypoxia. , 2015, American journal of physiology. Cell physiology.

[13]  Salah Ayoub,et al.  The Drosophila Embryo at Single Cell Transcriptome Resolution , 2017, bioRxiv.

[14]  Irving L. Weissman,et al.  Non-equivalence of Wnt and R-spondin ligands during Lgr5+ intestinal stem cell self-renewal , 2017, Nature.

[15]  Andrew J. Wilson,et al.  Gene expression profiling of intestinal epithelial cell maturation along the crypt-villus axis. , 2005, Gastroenterology.

[16]  Joseph T. Roland,et al.  Unsupervised Trajectory Analysis of Single-Cell RNA-Seq and Imaging Data Reveals Alternative Tuft Cell Origins in the Gut. , 2017, Cell systems.

[17]  Nicola Zamboni,et al.  Gut Microbiota Orchestrates Energy Homeostasis during Cold , 2015, Cell.

[18]  Hanlee P. Ji,et al.  Intestinal Enteroendocrine Lineage Cells Possess Homeostatic and Injury-Inducible Stem Cell Activity. , 2017, Cell stem cell.

[19]  Praveen Sethupathy,et al.  Functional Transcriptomics in Diverse Intestinal Epithelial Cell Types Reveals Robust MicroRNA Sensitivity in Intestinal Stem Cells to Microbial Status* , 2017, The Journal of Biological Chemistry.

[20]  T. Sutter,et al.  EGFR regulation of epidermal barrier function. , 2012, Physiological genomics.

[21]  Julian Lewis,et al.  Organizing cell renewal in the intestine: stem cells, signals and combinatorial control , 2006, Nature Reviews Genetics.

[22]  Aleksandra A. Kolodziejczyk,et al.  The technology and biology of single-cell RNA sequencing. , 2015, Molecular cell.

[23]  S. Quake,et al.  Transcriptomic characterization of 20 organs and tissues from mouse at single cell resolution creates a Tabula Muris , 2017, bioRxiv.

[24]  H. Clevers,et al.  Stem cells, self-renewal, and differentiation in the intestinal epithelium. , 2009, Annual review of physiology.

[25]  E. Elinav,et al.  Epithelial IL-18 Equilibrium Controls Barrier Function in Colitis , 2015, Cell.

[26]  Berthold Göttgens,et al.  Single-cell RNA-sequencing reveals a distinct population of proglucagon-expressing cells specific to the mouse upper small intestine , 2017, Molecular metabolism.

[27]  I. Amit,et al.  Single-cell spatial reconstruction reveals global division of labor in the mammalian liver , 2016, Nature.

[28]  Johannes E. Schindelin,et al.  Fiji: an open-source platform for biological-image analysis , 2012, Nature Methods.

[29]  J G Mabley,et al.  Inosine reduces inflammation and improves survival in a murine model of colitis. , 2003, American journal of physiology. Gastrointestinal and liver physiology.

[30]  G. Torres,et al.  Link between high‐affinity adenosine concentrative nucleoside transporter‐2 (CNT2) and energy metabolism in intestinal and liver parenchymal cells , 2010, Journal of cellular physiology.

[31]  A. Trautmann Extracellular ATP in the Immune System: More Than Just a “Danger Signal” , 2009, Science Signaling.

[32]  Pablo Tamayo,et al.  Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[33]  Fabian J Theis,et al.  The Human Cell Atlas , 2017, bioRxiv.

[34]  Hans Clevers,et al.  Single-cell messenger RNA sequencing reveals rare intestinal cell types , 2015, Nature.

[35]  Lior Pachter,et al.  Near-optimal probabilistic RNA-seq quantification , 2016, Nature Biotechnology.

[36]  L. Hooper,et al.  Symbiotic Bacteria Direct Expression of an Intestinal Bactericidal Lectin , 2006, Science.

[37]  Michael D. George,et al.  In vivo gene expression profiling of human intestinal epithelial cells: analysis by laser microdissection of formalin fixed tissues , 2008, BMC Genomics.

[38]  A. Regev,et al.  Spatial reconstruction of single-cell gene expression data , 2015 .

[39]  Stephan Saalfeld,et al.  Globally optimal stitching of tiled 3D microscopic image acquisitions , 2009, Bioinform..

[40]  J. Suez,et al.  A simple cage-autonomous method for the maintenance of the barrier status of germ-free mice during experimentation , 2014, Laboratory animals.

[41]  Shalev Itzkovitz,et al.  Spatial transcriptomics: paving the way for tissue-level systems biology. , 2017, Current opinion in biotechnology.

[42]  J. Marioni,et al.  High-throughput spatial mapping of single-cell RNA-seq data to tissue of origin , 2015, Nature Biotechnology.