Vol 76, No 4 (2017)
Original article
Published online: 2017-04-19

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Endothelial progenitor cells populate the stromal stem niche of tympanum

M. C. Rusu, V. S. Mănoiu, V. M. Popescu, R. C. Ciuluvică
Pubmed: 28553861
Folia Morphol 2017;76(4):630-634.

Abstract

The tympanic membrane (TM) integrity is of utmost importance for the sense of hearing. Therefore, the intrinsic potential of the TM to regenerate and repair deserves complete characterisation. Existing studies brought evidence on the epithelial stem niche of the TM. However, the stromal compartment was not evaluated for harbouring a distinctive stem, or progenitor, niche. We aimed doing this in transmission electron microscopy. We used TMs dissected out from 3 male Oryctolagus cuniculus rabbits. Evidence of stromal quiescent stem cells was gathered. Moreover, endothelial progenitor cells were found in the TM, being accurately identified by two specific ultrastructural markers of the endothelial lineage: the Weibel-Palade bodies and the stomatal diaphragms of the subplasmalemmal caveolae. The stromal stem niche of the TM appears to be a distinctive contributor during physiological and pathological processes of the TM, such as cholesteatoma formation, at least as a biological support for processes of vasculogenesis. However, further characterisation of the molecular pattern of the stromal stem niche of the TM is mandatory.

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References

  1. Boedts D. Tympanic epithelial migration. Clin Otolaryngol. 1978; 3(3): 249–253.
  2. Gladstone HB, Jackler RK, Varav K. Tympanic membrane wound healing. An overview. Otolaryngol Clin North Am. 1995; 28(5): 913–932.
  3. Hsu YC, Fuchs E. A family business: stem cell progeny join the niche to regulate homeostasis. Nat Rev Mol Cell Biol. 2012; 13(2): 103–114.
  4. Iannella G, Di Gioia C, Carletti R, et al. Tympanomastoid cholesterol granulomas: Immunohistochemical evaluation of angiogenesis. Laryngoscope. 2017; 127(8): E283–E290.
  5. Kim SW, Kim J, Seonwoo H, et al. Latent progenitor cells as potential regulators for tympanic membrane regeneration. Sci Rep. 2015; 5: 11542.
  6. Knutsson J, von Unge M, Rask-Andersen H. Localization of progenitor/stem cells in the human tympanic membrane. Audiol Neurootol. 2011; 16(4): 263–269.
  7. Makino K, Amatsu M, Kinishi M, et al. Epithelial migration in the healing process of tympanic membrane perforations. Eur Arch Otorhinolaryngol. 1990; 247(6): 352–355.
  8. Palade GE, Bruns RR. Structural modulations of plasmalemmal vesicles. J Cell Biol. 1968; 37(3): 633–649.
  9. Perlea P, Rusu MC, Didilescu AC, et al. Phenotype heterogeneity in dental pulp stem niches. Rom J Morphol Embryol. 2016; 57(4): 1187–1193.
  10. Rusu MC, Hostiuc S, Vrapciu AD, et al. Subsets of telocytes: Myocardial telocytes. Ann Anat. 2017; 209: 37–44.
  11. Stan RV. Structure of caveolae. Biochim Biophys Acta. 2005; 1746(3): 334–348.
  12. Stan RV. Endothelial stomatal and fenestral diaphragms in normal vessels and angiogenesis. J Cell Mol Med. 2007; 11(4): 621–643.
  13. Stan RV, Tkachenko E, Niesman IR. PV1 is a key structural component for the formation of the stomatal and fenestral diaphragms. Mol Biol Cell. 2004; 15(8): 3615–3630.
  14. Sudhoff H, Dazert S, Gonzales AM, et al. Angiogenesis and angiogenic growth factors in middle ear cholesteatoma. Am J Otol. 2000; 21(6): 793–798.
  15. Weibel ER. Fifty years of Weibel-Palade bodies: the discovery and early history of an enigmatic organelle of endothelial cells. J Thromb Haemost. 2012; 10(6): 979–984.
  16. Zimmerlin L, Donnenberg VS, Donnenberg AD. Pericytes: a universal adult tissue stem cell? Cytometry A. 2012; 81(1): 12–14.