Hostname: page-component-cd9895bd7-mkpzs Total loading time: 0 Render date: 2024-12-29T06:55:40.407Z Has data issue: false hasContentIssue false

Cell origin in the macula flava of the human newborn vocal fold

Published online by Cambridge University Press:  06 May 2016

K Sato*
Affiliation:
Department of Otolaryngology – Head and Neck Surgery, Kurume University School of Medicine, Japan
S Chitose
Affiliation:
Department of Otolaryngology – Head and Neck Surgery, Kurume University School of Medicine, Japan
T Kurita
Affiliation:
Department of Otolaryngology – Head and Neck Surgery, Kurume University School of Medicine, Japan
H Umeno
Affiliation:
Department of Otolaryngology – Head and Neck Surgery, Kurume University School of Medicine, Japan
*
Address for correspondence: Dr Kiminori Sato, Department of Otolaryngology – Head and Neck Surgery, Kurume University School of Medicine, 67 Asahi-machi, Kurume 830-0011, Japan Fax: +81 942 37 1200 E-mail: kimisato@oct-net.ne.jp

Abstract

Background:

There is growing evidence to suggest that cells in the maculae flavae are tissue stem cells of the human vocal fold and maculae flavae are a stem cell niche.

Methods:

Three newborn vocal folds were investigated. Immunoreactivity to antibodies directed to cytokeratin, desmin, glial fibrillary acidic protein, vimentin, cluster of differentiation 34, cluster of differentiation 45, collagen type I, telomerase reverse transcriptase, SOX17 and stage-specific embryonic antigen 3 was investigated.

Results:

The cells in the newborn maculae flavae expressed haematopoietic markers (cluster of differentiation 34, cluster of differentiation 45) and collagen type I, which are the major makers of bone marrow derived circulating fibrocytes. The cells expressed epithelium, muscle, neural and mesenchymal cell associated proteins, and endodermal marker, indicating that they are undifferentiated and express proteins of all three germ layers. The cells also expressed stage-specific embryonic antigen 3 and telomerase reverse transcriptase.

Conclusion:

The cells in the newborn maculae flavae are undifferentiated cells arising from the differentiation of bone marrow cells. The results of this study are consistent with the hypothesis that the cells in maculae flavae are tissue stem cells.

Type
Main Articles
Copyright
Copyright © JLO (1984) Limited 2016 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

Footnotes

Presented (and awarded Poster Presentation Second Place Award) at the 95th Annual Meeting of the American Broncho-Esophagological Association, 22–23 April 2015, Boston, Massachusetts, USA.

References

1Hirano, M, Sato, K. Histological Color Atlas of the Human Larynx. San Diego: Singular Publishing Group, 1993Google Scholar
2Sato, K, Hirano, M, Nakashima, T. Stellate cells in the human vocal fold. Ann Otol Rhinol Laryngol 2001;110:319–25Google Scholar
3Sato, K, Hirano, M, Nakashima, T. Vitamin A-storing stellate cells in the human vocal fold. Acta Otolaryngol 2003;123:106–10Google Scholar
4Sato, K, Umeno, H, Nakashima, T. Functional histology of the macula flava in the human vocal fold. Part 1: Its roles in the adult vocal fold. Folia Phoniatr Logop 2010;62:178–84Google Scholar
5Sato, K, Hirano, M, Nakashima, T. Fine structure of the human newborn and infant vocal fold mucosae. Ann Otol Rhinol Laryngol 2001;110:417–24Google Scholar
6Sato, K, Nakashima, T. Vitamin A-storing stellate cells in the human newborn vocal fold. Ann Otol Rhinol Laryngol 2005;114:517–24CrossRefGoogle ScholarPubMed
7Sato, K, Umeno, H, Nakashima, T. Functional histology of the macula flava in the human vocal fold. Part 2: Its roles in the growth and development of the vocal fold. Folia Phoniatr Logop 2010;62:263–70Google Scholar
8Sato, K, Hirano, M, Nakashima, T. Age-related changes in vitamin A-storing stellate cells of human vocal fold. Ann Otol Rhinol Laryngol 2004;113:108–12Google Scholar
9Sato, K, Umeno, H, Nakashima, T. Vocal fold stellate cells in the human macula flava and the diffuse stellate cell system. Ann Otol Rhinol Laryngol 2012;121:51–6CrossRefGoogle ScholarPubMed
10Sato, K, Umeno, T, Nakashima, T. Vocal fold stem cells and their niche in the human vocal fold. Ann Otol Rhinol Laryngol 2012;121:798803Google Scholar
11Kurita, T, Sato, K, Chitose, S, Fukahori, M, Sueyoshi, S, Umeno, H. Origin of vocal fold stellate cells in the human macula flava. Ann Otol Rhinol Laryngol 2015;124:698705Google Scholar
12Xie, T, Li, L. Stem cell niche: structure and function. Annu Rev Cell Dev Biol 2005;21:605–31Google Scholar
13Becker, W, Kleinsmith, L, Hardin, J. Intermediate filament. In: The World of the Cell, 6th edn.San Francisco: Benjamin Cummings, 2006;446–50Google Scholar
14Becker, WM, Kleinsmith, LJ, Hardin, J. The cell cycle, DNA replication, and mitosis. In: The World of the Cell, 6th edn.San Francisco: Benjamin Cummings, 2006;554–71Google Scholar
15Friedenstein, AJ, Deriglasova, UF, Kulagina, NN, Panasuk, AF, Rudakowa, SF, Luria, EA et al. Precursors for fibroblasts in different populations of hematopoietic cells as detected by the in vitro colony assay method. Exp Hematol 1974;2:8392Google ScholarPubMed
16Deasy, BM. Asymmetric behavior in stem cells. In: Rajasekhar, VK, ed. Regulatory Networks in Stem Cells. New York: Humana Press, 2009;1325Google Scholar
17Sato, K, Chitose, S, Kurita, T, Umeno, H. Microenvironment of macula flava in the human vocal fold as a stem cell niche. J Laryngol Otol [in press]Google Scholar
18Abedi, M. Hematopoietic origin of fibrocytes. In: Bucala, R, ed. Fibrocytes in Health and Disease. Singapore: World Scientific Publishing, 2012;115Google Scholar
19Forbes, SJ, Russo, FP, Rey, V, Burra, P, Wright, NA, Alison, MR. A significant proportion of myofibroblasts are of bone marrow origin in human liver fibrosis. Gastroenterology 2004;126:955–63Google Scholar
20Brittan, M, Hunt, T, Jeffery, R, Poulsom, R, Forbes, SJ, Hodivala-Dilke, K et al. Bone marrow derivation of pericryptal myofibroblasts in the mouse and human small intestine and colon. Gut 2002;50:752–7Google Scholar
21Bucala, R, Spiegel, LA, Chesney, J, Hogan, M, Cerami, A. Circulating fibrocytes define a new leukocyte subpopulation that mediates tissue repair. Mol Med 1994;1:7181Google Scholar
22Yamashita, M, Hirano, S, Manemaru, S, Tsuji, S, Suehiro, A, Ito, J. Side population cells in the human vocal fold. Ann Otol Rhinol Laryngol 2007;116:847–52Google Scholar
23Gugatschka, M, Kojima, T, Ohno, S, Kanemaru, S, Hirano, S. Recruitment patterns of side population cells during wound healing in rat vocal folds. Laryngoscope 2011;121:1662–7Google Scholar
24Fishman, JM, Long, J, Gugatschka, M, De Coppi, P, Hirano, S, Hertegard, S et al. Stem cell approaches for vocal fold regeneration. Laryngoscope 2016. Epub 2016 Jan 17Google Scholar