Thymus formation in uncharted embryonic territories

The thymus is a conserved organ among vertebrates, derived from the endoderm of distinct pharyngeal pouches (PP), whose location and number vary across species. Together with reports of sporadic ectopic thymus locations in mice and humans, this suggests that the potential to make a thymus resides in a broader region of the PP endoderm than previously ascribed. Using the chick-quail chimera system, we explore this hypothesis and test the capacity of non-canonical pouches to participate in thymus formation. We further ask if the local mesenchyme of pharyngeal arches (PA) could also play a role in the regulation of thymus formation. After testing several embryonic tissue associations, we mapped the pharyngeal endoderm regions with thymus potential to the second and third/fourth pharyngeal pouches (2PP and 3/4PP). We further identified mesenchyme regions that regulate this potential to the 3/4 pharyngeal arches and to the dorsal region of the second arch, with positive and negative influences, respectively. Transcriptomic analysis of these tissues helped us revealing a common genetic program in the PP endoderm linked to thymus potential in addition to finding distinct signalling pathways involved in the cellular interactions with the mesenchyme of the pharyngeal arches that result in modulating this potential. Together, these results provide new information about the initial specification of thymus primordia in the embryo that may contribute to improving the development of thymus organoid systems. Graphical abstract

[1]  Y. Ohe,et al.  Insulinoma-associated-1 (INSM1) expression in thymic squamous cell carcinoma. , 2022, Virchows Archiv : an international journal of pathology.

[2]  Arif Istiaq,et al.  A review on Tsukushi: mammalian development, disorders, and therapy. , 2022, Journal of cell communication and signaling.

[3]  Fabian J Theis,et al.  Integration of single-cell transcriptomes and chromatin landscapes reveals regulatory programs driving pharyngeal organ development , 2022, Nature Communications.

[4]  Kailin Xu,et al.  Thymus Degeneration and Regeneration , 2021, Frontiers in Immunology.

[5]  Mark S. Anderson,et al.  Single-cell transcriptional profiling of human thymic stroma uncovers novel cellular heterogeneity in the thymic medulla , 2021, Nature Communications.

[6]  W. Chan,et al.  Hoxb3 Regulates Jag1 Expression in Pharyngeal Epithelium and Affects Interaction With Neural Crest Cells , 2021, Frontiers in Physiology.

[7]  H. Neves,et al.  Thymus Inception: Molecular Network in the Early Stages of Thymus Organogenesis , 2020, International journal of molecular sciences.

[8]  Chengji J. Zhou,et al.  Genetics and signaling mechanisms of orofacial clefts , 2020, Birth defects research.

[9]  S. Teichmann,et al.  A cell atlas of human thymic development defines T cell repertoire formation , 2020, Science.

[10]  Y. Saeys,et al.  NicheNet: modeling intercellular communication by linking ligands to target genes , 2019, Nature Methods.

[11]  H. Neves,et al.  Isolation of Embryonic Tissues and Formation of Quail-Chicken Chimeric Organs Using The Thymus Example. , 2019, Journal of visualized experiments : JoVE.

[12]  Chengji J. Zhou,et al.  Wnt signaling in orofacial clefts: crosstalk, pathogenesis and models , 2019, Disease Models & Mechanisms.

[13]  T. Boehm,et al.  Elevated levels of Wnt signaling disrupt thymus morphogenesis and function , 2017, Scientific Reports.

[14]  J. C. Silva,et al.  Notch and Hedgehog in the thymus/parathyroid common primordium: Crosstalk in organ formation. , 2016, Developmental biology.

[15]  S. Zaffran,et al.  Disruption of CXCR4 signaling in pharyngeal neural crest cells causes DiGeorge syndrome-like malformations , 2016, Development.

[16]  Y. Hamazaki Adult thymic epithelial cell (TEC) progenitors and TEC stem cells: Models and mechanisms for TEC development and maintenance , 2015, European journal of immunology.

[17]  S. Woods,et al.  The obesity-associated transcription factor ETV5 modulates circulating glucocorticoids , 2015, Physiology & Behavior.

[18]  D. Bayarsaihan,et al.  Genome-wide Chromatin Mapping Defines AP2α in the Etiology of Craniofacial Disorders , 2015, The Cleft palate-craniofacial journal : official publication of the American Cleft Palate-Craniofacial Association.

[19]  Matthew E. Ritchie,et al.  limma powers differential expression analyses for RNA-sequencing and microarray studies , 2015, Nucleic acids research.

[20]  Paul Theodor Pyl,et al.  HTSeq – A Python framework to work with high-throughput sequencing data , 2014, bioRxiv.

[21]  Andreia J. Amaral,et al.  Quality assessment and control of tissue specific RNA-seq libraries of Drosophila transgenic RNAi models , 2014, Front. Genet..

[22]  Charity W. Law,et al.  voom: precision weights unlock linear model analysis tools for RNA-seq read counts , 2014, Genome Biology.

[23]  N. Manley,et al.  Transdifferentiation of parathyroid cells into cervical thymi promotes atypical T cell development , 2013, Nature Communications.

[24]  V. Hamburger,et al.  A series of normal stages in the development of the chick embryo. 1951. , 2012, Developmental dynamics : an official publication of the American Association of Anatomists.

[25]  E. Dupin,et al.  Modulation of Bmp4 signalling in the epithelial-mesenchymal interactions that take place in early thymus and parathyroid development in avian embryos. , 2012, Developmental biology.

[26]  T. Hosoya,et al.  MafB interacts with Gcm2 and regulates parathyroid hormone expression and parathyroid development , 2011, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[27]  J. Muñoz,et al.  Eph/Ephrin-Mediated Interactions in the Thymus , 2011, Neuroimmunomodulation.

[28]  A. Graham,et al.  Shh signalling restricts the expression of Gcm2 and controls the position of the developing parathyroids. , 2011, Developmental biology.

[29]  Marcel Martin Cutadapt removes adapter sequences from high-throughput sequencing reads , 2011 .

[30]  B. Morrow,et al.  A Tbx1-Six1/Eya1-Fgf8 genetic pathway controls mammalian cardiovascular and craniofacial morphogenesis. , 2011, The Journal of clinical investigation.

[31]  Cathrin Brisken,et al.  Control of hair follicle cell fate by underlying mesenchyme through a CSL-Wnt5a-FoxN1 regulatory axis. , 2010, Genes & development.

[32]  D. Kioussis,et al.  EphB–ephrin-B2 interactions are required for thymus migration during organogenesis , 2010, Proceedings of the National Academy of Sciences.

[33]  N. Manley,et al.  Evidence for an early role for BMP4 signaling in thymus and parathyroid morphogenesis. , 2010, Developmental biology.

[34]  Darrell J. R. Evans,et al.  Developmental stages of the Japanese quail , 2010, Journal of anatomy.

[35]  M. C. Jørgensen,et al.  Retinoic Acid Signaling Organizes Endodermal Organ Specification along the Entire Antero-Posterior Axis , 2009, PloS one.

[36]  R. Lovell-Badge,et al.  SOX3 activity during pharyngeal segmentation is required for craniofacial morphogenesis , 2007, Development.

[37]  N. Manley,et al.  Bmp4 and Noggin expression during early thymus and parathyroid organogenesis. , 2006, Gene expression patterns : GEP.

[38]  J. Reimann,et al.  Evidence for a Functional Second Thymus in Mice , 2006, Science.

[39]  T. Boehm,et al.  BMP Signaling Is Required for Normal Thymus Development1 , 2005, The Journal of Immunology.

[40]  P. Carmeliet,et al.  Gene targeting of VEGF-A in thymus epithelium disrupts thymus blood vessel architecture. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[41]  N. Manley,et al.  Differential expression of Sonic hedgehog along the anterior-posterior axis regulates patterning of pharyngeal pouch endoderm and pharyngeal endoderm-derived organs. , 2005, Developmental biology.

[42]  A. Varas,et al.  Reduced Thymocyte Development in Sonic Hedgehog Knockout Embryos 1 , 2004, The Journal of Immunology.

[43]  C. Glass,et al.  Eya protein phosphatase activity regulates Six1–Dach–Eya transcriptional effects in mammalian organogenesis , 2003, Nature.

[44]  L. Jerome-Majewska,et al.  Aortic arch and pharyngeal phenotype in the absence of BMP-dependent neural crest in the mouse , 2002, Mechanisms of Development.

[45]  C. Dickson,et al.  Development of the Thymus Requires Signaling Through the Fibroblast Growth Factor Receptor R2-IIIb , 2001, The Journal of Immunology.

[46]  N. Manley,et al.  Hoxa3 and pax1 regulate epithelial cell death and proliferation during thymus and parathyroid organogenesis. , 2001, Developmental biology.

[47]  H. Etchevers,et al.  The cephalic neural crest provides pericytes and smooth muscle cells to all blood vessels of the face and forebrain. , 2001, Development.

[48]  G. Morahan,et al.  The nu gene acts cell-autonomously and is required for differentiation of thymic epithelial progenitors. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[49]  B. Kyewski,et al.  Two Genetically Separable Steps in the Differentiation of Thymic Epithelium , 1996, Science.

[50]  David Ish-Horowicz,et al.  Expression of a Delta homologue in prospective neurons in the chick , 1995, Nature.

[51]  P. Gruss,et al.  undulated phenotypes suggest a role of Pax-1 for the development of vertebral and extravertebral structures. , 1995, Developmental biology.

[52]  Thomas Boehm,et al.  New member of the winged-helix protein family disrupted in mouse and rat nude mutations , 1994, Nature.

[53]  F. Jotereau,et al.  Tracing of cells of the avian thymus through embryonic life in interspecific chimeras , 1975, The Journal of experimental medicine.

[54]  V. Hamburger,et al.  A series of normal stages in the development of the chick embryo , 1951, Journal of morphology.

[55]  J. Dyke On the origin of accessory thymus tissue, thymus IV: The occurrence in man , 1941 .

[56]  R. Krumlauf,et al.  A Hox gene regulatory network for hindbrain segmentation. , 2020, Current topics in developmental biology.

[57]  S. Brunak,et al.  A scored human protein–protein interaction network to catalyze genomic interpretation , 2017, Nature Methods.

[58]  Thomas R. Gingeras,et al.  STAR: ultrafast universal RNA-seq aligner , 2013, Bioinform..

[59]  A. Groves,et al.  Expression of the Foxi2 and Foxi3 transcription factors during development of chicken sensory placodes and pharyngeal arches. , 2013, Gene expression patterns : GEP.

[60]  H. Neves,et al.  The role of Notch signaling in thymic epithelium development , 2011 .

[61]  T. Young,et al.  Hox, Cdx, and anteroposterior patterning in the mouse embryo. , 2009, Current topics in developmental biology.

[62]  H. Rodewald Thymus organogenesis. , 2008, Annual review of immunology.

[63]  S. Creuzet,et al.  The contribution of the neural crest to the vertebrate body. , 2006, Advances in experimental medicine and biology.

[64]  R. Balling,et al.  Pax1 is expressed during development of the thymus epithelium and is required for normal T-cell maturation. , 1996, Development.

[65]  N. L. Le Douarin,et al.  Mesenchymal derivatives of the neural crest: analysis of chimaeric quail and chick embryos. , 1975, Journal of embryology and experimental morphology.