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Complex Mammalian-like Hematopoietic System Found in a Colonial Chordate

Hematopoiesis is an essential process that evolved in multicellular animals. At the heart of this process are hematopoietic stem cells (HSCs), which are multipotent, self-renewing and generate the entire repertoire of blood and immune cells throughout an animal’s life(1). While there are comprehensi...

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Detalles Bibliográficos
Autores principales: Rosental, Benyamin, Kowarsky, Mark, Seita, Jun, Corey, Daniel M., Ishizuka, Katherine J., Palmeri, Karla J., Chen, Shih-Yu, Sinha, Rahul, Okamoto, Jennifer, Mantalas, Gary, Manni, Lucia, Raveh, Tal, Clarke, D. Nathaniel, Tsai, Jonathan M., Newman, Aaron M., Neff, Norma F., Nolan, Garry P., Quake, Stephen R., Weissman, Irving L., Voskoboynik, Ayelet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6347970/
https://www.ncbi.nlm.nih.gov/pubmed/30518860
http://dx.doi.org/10.1038/s41586-018-0783-x
Descripción
Sumario:Hematopoiesis is an essential process that evolved in multicellular animals. At the heart of this process are hematopoietic stem cells (HSCs), which are multipotent, self-renewing and generate the entire repertoire of blood and immune cells throughout an animal’s life(1). While there are comprehensive studies on vertebrate HSC self-renewal, differentiation, physiological regulation and niche occupation, relatively little is known about their evolutionary origin and their niches. Here we study the hematopoietic system of Botryllus schlosseri, a colonial tunicate that has vasculature, circulating blood cells, and interesting stem cell biology and immunity characteristics(2–8). Self-recognition between genetically compatible B. schlosseri colonies leads to the formation of natural parabionts with shared circulation, whereas incompatible colonies reject each other (3,4,7). Using flow-cytometry, whole-transcriptome sequencing of defined cell populations and diverse functional assays, we identified HSCs, progenitors, immune-effector cells, and an HSC niche, and demonstrated that self-recognition inhibits allospecific cytotoxic reactions. Our study reveals that HSC and myeloid lineage immune cells emerged in a common ancestor of tunicates and vertebrates, and these results also suggest that hematopoietic bone marrow and the B. schlosseri endostyle niche evolved from a common origin.