TY - JOUR
T1 - How to prevent contamination with Candida albicans during the fabrication of transplantable oral mucosal epithelial cell sheets
AU - Takagi, Ryo
AU - Kobayashi, Shinichiro
AU - Yamato, Masayuki
AU - Owaki, Toshiyuki
AU - Kasai, Yoshiyuki
AU - Hosoi, Takahiro
AU - Sakai, Yusuke
AU - Kanetaka, Kengo
AU - Minamizato, Tokutaro
AU - Minematsu, Asuka
AU - Kondo, Makoto
AU - Kanai, Nobuo
AU - Yamaguchi, Naoyuki
AU - Nagai, Kazuhiro
AU - Miyazaki, Yasushi
AU - Takeda, Naoya
AU - Fukai, Fumio
AU - Asahina, Izumi
AU - Miyazaki, Taiga
AU - Kohno, Shigeru
AU - Yamamoto, Masakazu
AU - Nakao, Kazuhiko
AU - Eguchi, Susumu
AU - Okano, Teruo
N1 - Publisher Copyright:
© 2015 the Japanese Society for Regenerative Medicine.
PY - 2015/6/1
Y1 - 2015/6/1
N2 - We have utilized patients' own oral mucosa as a cell source for the fabrication of transplantable epithelial cell sheets to treat limbal stem cell deficiency and mucosal defects after endoscopic submucosal dissection of esophageal cancer. Because there are abundant microbiotas in the human oral cavity, the oral mucosa was sterilized and 40μg/mL gentamicin and 0.27μg/mL amphotericin B were added to the culture medium in our protocol. Although an oral surgeon carefully checked each patient's oral cavity and although candidiasis was not observed before taking the biopsy, contamination with Candida albicans (C.albicans) was detected in the conditioned medium during cell sheet fabrication. After adding 1μg/mL amphotericin B to the transportation medium during transport from Nagasaki University Hospital to Tokyo Women's Medical University, which are 1200km apart, no proliferation of C.albicans was observed. These results indicated that the supplementation of transportation medium with antimycotics would be useful for preventing contamination with C.albicans derived from the oral mucosa without hampering cell proliferation.
AB - We have utilized patients' own oral mucosa as a cell source for the fabrication of transplantable epithelial cell sheets to treat limbal stem cell deficiency and mucosal defects after endoscopic submucosal dissection of esophageal cancer. Because there are abundant microbiotas in the human oral cavity, the oral mucosa was sterilized and 40μg/mL gentamicin and 0.27μg/mL amphotericin B were added to the culture medium in our protocol. Although an oral surgeon carefully checked each patient's oral cavity and although candidiasis was not observed before taking the biopsy, contamination with Candida albicans (C.albicans) was detected in the conditioned medium during cell sheet fabrication. After adding 1μg/mL amphotericin B to the transportation medium during transport from Nagasaki University Hospital to Tokyo Women's Medical University, which are 1200km apart, no proliferation of C.albicans was observed. These results indicated that the supplementation of transportation medium with antimycotics would be useful for preventing contamination with C.albicans derived from the oral mucosa without hampering cell proliferation.
KW - Amphotericin B
KW - C.albicans
KW - Candida albicans
KW - DMEM
KW - Oral mucosal epithelial cell
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U2 - 10.1016/j.reth.2014.12.002
DO - 10.1016/j.reth.2014.12.002
M3 - Article
AN - SCOPUS:85041046557
SN - 2352-3204
VL - 1
SP - 1
EP - 4
JO - Regenerative Therapy
JF - Regenerative Therapy
ER -