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Purinergic signaling pathway in human olfactory neuronal precursor cells

dc.contributor.authorSolís Chagoyan, Héctor
dc.contributor.authorFlores Soto, Edgar
dc.contributor.authorValdés Tovar, Marcela
dc.contributor.authorCercós, Montserrat G.
dc.contributor.authorCalixto, Eduardo
dc.contributor.authorMontaño, Luis M.
dc.contributor.authorBarajas López, Carlos
dc.contributor.authorSommer, Bettina
dc.contributor.authorAquino Galvez, Arnoldo
dc.contributor.authorTrueta, Citlali
dc.contributor.authorBenítez King, Gloria Acacia
dc.date.accessioned2020-03-04T00:53:24Z
dc.date.available2020-03-04T00:53:24Z
dc.date.issued2019
dc.identifier.citationSolís-Chagoyán, Héctor & Flores-Soto, Edgar & Valdés, Marcela & Cercós, Montserrat & Calixto, Eduardo & Montaño, Luis & Barajas-López, Carlos & Sommer, Bettina & Aquino-Galvez, Arnoldo & Trueta, Citlali & Benítez-King, Gloria. (2019). Purinergic Signaling Pathway in Human Olfactory Neuronal Precursor Cells. Stem Cells International. 2019. 1-17. 10.1155/2019/2728786.
dc.identifier.urihttp://hdl.handle.net/11627/5290
dc.description.abstract"Extracellular ATP and trophic factors released by exocytosis modulate in vivo proliferation, migration, and differentiation in multipotent stem cells (MpSC); however, the purinoceptors mediating this signaling remain uncharacterized in stem cells derived from the human olfactory epithelium (hOE). Our aim was to determine the purinergic pathway in isolated human olfactory neuronal precursor cells (hONPC) that exhibit MpSC features. Cloning by limiting dilution from a hOE heterogeneous primary culture was performed to obtain a culture predominantly constituted by hONPC. Effectiveness of cloning to isolate MpSC-like precursors was corroborated through immunodetection of specific protein markers and by functional criteria such as self-renewal, proliferation capability, and excitability of differentiated progeny. P2 receptor expression in hONPC was determined by Western blot, and the role of these purinoceptors in the ATP-induced exocytosis and changes in cytosolic Ca2+ ([Ca2+]i) were evaluated using the fluorescent indicators FM1-43 and Fura-2 AM, respectively. The clonal culture was enriched with SOX2 and OCT3/4 transcription factors; additionally, the proportion of nestin-immunopositive cells, the proliferation capability, and functionality of differentiated progeny remained unaltered through the long-term clonal culture. hONPC expressed P2X receptor subtypes 1, 3-5, and 7, as well as P2Y2, 4, 6, and 11; ATP induced both exocytosis and a transient [Ca2+]i increase predominantly by activation of metabotropic P2Y receptors. Results demonstrated for the first time that ex vivo-expressed functional P2 receptors in MpSC-like hONPC regulate exocytosis and Ca2+ signaling. This purinergic-triggered release of biochemical messengers to the extracellular milieu might be involved in the paracrine signaling among hOE cells."
dc.publisherHindawi Publishing Corporation
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.classificationBIOLOGÍA CELULAR
dc.titlePurinergic signaling pathway in human olfactory neuronal precursor cells
dc.typearticle
dc.identifier.doihttps://doi.org/10.1155/2019/2728786
dc.rights.accessAcceso Abierto


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Attribution-NonCommercial-NoDerivatives 4.0 Internacional
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internacional