Carnosine immunohistochemistry in human olfactory mucosa

1990 ◽  
Vol 15 ◽  
pp. S97
Author(s):  
Masao Sakai ◽  
Makoto Ashihara ◽  
Tadao Nishimura ◽  
Ikuko Nagatsu
2021 ◽  
Vol 1 (19) ◽  
pp. 75-77
Author(s):  
O.V. Stepanova ◽  
E.K. Karsuntseva ◽  
G.A. Fursa ◽  
A.V. Chadin ◽  
M.P. Valikhov ◽  
...  

Enriched cultures of olfactory ensheathing cells and neural stem/progenitor cells were obtained according to our developed protocols from the olfactory mucosa of rat and human. It has been shown that only transplantation of human and rat olfactory ensheathing cells leads to a significant decrease in the size of cysts, as well as their complete disappearance in some animals.


Author(s):  
Wen-Hui Feng ◽  
John S. Kauer ◽  
Lester Adelman ◽  
Barbara R. Talamo

Life Sciences ◽  
2021 ◽  
Vol 265 ◽  
pp. 118861
Author(s):  
Jialin He ◽  
Yan Huang ◽  
Jianyang Liu ◽  
Lite Ge ◽  
Xiangqi Tang ◽  
...  

2005 ◽  
Vol 115 (12) ◽  
pp. 2144-2154 ◽  
Author(s):  
Eric H. Holbrook ◽  
Donald A. Leopold ◽  
James E. Schwob

1982 ◽  
Vol 108 (4) ◽  
pp. 247-249 ◽  
Author(s):  
M. A. Lovell ◽  
B. W. Jafek ◽  
D. T. Moran ◽  
J. C. Rowley

1992 ◽  
Vol 106 (2) ◽  
pp. 181-188 ◽  
Author(s):  
Tuesday K. Mellert ◽  
Marilyn L. Getchell ◽  
Larry Sparks ◽  
Thomas V. Getchell

Immunologic defense factors in the human olfactory mucosa were localized immunohistochemically. Olfactory epithelium was identified with an antiserum to olfactory marker protein, specific for olfactory receptor neurons. Constituents of the secretory immune system, including IgA, IgM, secretory component, and J chain, were localized in the acinar and duct cells of Bowman's glands and in the mucociliary complex. In addition, B lymphocytes in the lamina propria near Bowman's glands displayed immunoreactivity for IgA, IgM, and J chain. Immunostaining also localized other humoral factors. Immunoreactivity for IgG was present throughout the stroma and in B lymphocytes in the lamina propria. Antibody to IgD stained numerous B lymphocytes clustered below the basement membrane. Antibody to IgE stained similarly distributed cells; toluidine blue staining demonstrated that many were mast cells. In addition, antibodies to IgD and IgE stained occasional intraepithelial B lymphocytes or mast cells. Two antimicrobial proteins, lactoferrin and lysozyme, were localized in Bowman's glands and the mucociliary complex. Thus, the human olfactory mucosa, which provides a direct neural route for pathogens to the brain, is a site for synthesis and secretion of immune and other defense factors.


2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Gerardo Santiago-Toledo ◽  
Melanie Georgiou ◽  
Joana dos Reis ◽  
Victoria H. Roberton ◽  
Ana Valinhas ◽  
...  

Abstract Human olfactory mucosa cells (hOMCs) have been transplanted to the damaged spinal cord both pre-clinically and clinically. To date mainly autologous cells have been tested. However, inter-patient variability in cell recovery and quality, and the fact that the neuroprotective olfactory ensheathing cell (OEC) subset is difficult to isolate, means an allogeneic hOMC therapy would be an attractive “off-the-shelf” alternative. The aim of this study was to generate a candidate cell line from late-adherent hOMCs, thought to contain the OEC subset. Primary late-adherent hOMCs were transduced with a c-MycERTAM gene that enables cell proliferation in the presence of 4-hydroxytamoxifen (4-OHT). Two c-MycERTAM-derived polyclonal populations, PA5 and PA7, were generated and expanded. PA5 cells had a normal human karyotype (46, XY) and exhibited faster growth kinetics than PA7, and were therefore selected for further characterisation. PA5 hOMCs express glial markers (p75NTR, S100ß, GFAP and oligodendrocyte marker O4), neuronal markers (nestin and ß-III-tubulin) and fibroblast-associated markers (CD90/Thy1 and fibronectin). Co-culture of PA5 cells with a neuronal cell line (NG108-15) and with primary dorsal root ganglion (DRG) neurons resulted in significant neurite outgrowth after 5 days. Therefore, c-MycERTAM-derived PA5 hOMCs have potential as a regenerative therapy for neural cells.


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