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Characterization of human upper airway epithelial progenitors
Author(s) -
Bravo Dawn T.,
Soudry Ethan,
Edward Justin A.,
Le Wei,
Nguyen Alan L.,
Hwang Peter H.,
Sanyal Mrinmoy,
Nayak Jayakar V.
Publication year - 2013
Publication title -
international forum of allergy and rhinology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.503
H-Index - 46
eISSN - 2042-6984
pISSN - 2042-6976
DOI - 10.1002/alr.21205
Subject(s) - progenitor cell , epithelial cell adhesion molecule , population , microbiology and biotechnology , pathology , medicine , stem cell , respiratory epithelium , immunology , biology , cell adhesion molecule , epithelium , environmental health
Background New epithelial cells are generated through the proliferation and differentiation of resident progenitor cells in the nasal cavity. In several upper airway diseases, such as cystic fibrosis and chronic rhinosinusitis, self‐renewing progenitor cells may be functionally defective, or compromised in their ability, to regenerate cells that maintain normal mucociliary clearance. Herein, we describe our early work to define and characterize a rare population of human nasal epithelial putative progenitors. Methods Single‐cell suspensions of human ethmoid sinus tissues were prepared following endoscopic sinus surgery. Cell surface antibodies were analyzed as candidate markers for detecting progenitor cells. A panel of antibodies, including epithelial cell adhesion molecule (EpCAM, epithelial cells), CD45 (hematopoietic cells), nerve growth factor receptor (NGFR/CD271), intercellular adhesion molecule‐1 (ICAM1/CD54), and integrin‐α6 (ITGA6/CD49f) were used to resolve epithelial progenitor candidates by high‐dimensional flow cytometry and the gating technique of fluorescence minus one (FMO) controls. Results A rare population of approximately 0.06% of total ethmoid cells was discriminated as EpCAM − CD45 − NGFR + ICAM1 + by surface markers. Use of ITGA6 was excluded based on FMO control analysis. This lineage‐negative population was purified to 99% homogeneity by cell sorting and analyzed by immunofluorescence microscopy. Sorted cells were subsequently confirmed to uniformly express the transcription factor p63. Upon in vitro culture, lineage‐negative clonal cells were confirmed to spontaneously differentiate into epithelial lineage‐positive cells. Conclusion Using the NGFR and ICAM1 cellular coordinates, we have identified a promising population of native human nasal epithelial progenitor cells that require more formal investigation for their role in upper airway regeneration.