TY - JOUR
T1 - The air liquid-interface, a skin microenvironment, promotes growth of melanoma cells, but not their apoptosis and invasion, through activation of mitogen-activated protein kinase
AU - Yee, Chong Hong
AU - Aoki, Shigehisa
AU - Uchihashi, Kazuyoshi
AU - Matsunobu, Aki
AU - Yamasaki, Fumio
AU - Misago, Noriyuki
AU - Piao, Meihua
AU - Tetsuji, Uemura
AU - Yonemitsu, Nobuhisa
AU - Sugihara, Hajime
AU - Toda, Shuji
PY - 2010/2/27
Y1 - 2010/2/27
N2 - The air-liquid interface (ALI) is a common microenvironment of the skin, but it is unknown whether the ALI affects melanoma cell behaviors. Using a collagen gel invasion assay, immuno histochemistry, and Western blots, here we show that melanoma cell proliferation in cultures with an ALI is higher than melanoma cell proliferation in submerged cultures. Bromodeoxyuridine (BrdU) uptake, an indicator of cell proliferation, of melanoma cells at the ALI was about 3 times that of submerged cells, while ALI and submerged melanoma cells had similar levels of single-stranded DNA (a marker of apoptosis). The ALI enhanced the expression of Raf-1, MEK-1 and pERK-1/2 components of the mitogen-activated protein kinase (MAPK) cascade, in cells more than the submerged condition did. The increases in BrdU uptake and pERK-1/2 expression promoted by ALI was abolished by the MEK inhibitor, PD-98059. ALI-treated and submerged melanoma cells did not infiltrate into the collagen gel, and they showed no significant difference in the expression of the invasion and motility-related molecules, matrix metalloproteinase-1 and -9, laminin 5, and filamin A. Our data indicate that the ALI, a skin microenvironment, accelerates the growth, but not the apoptosis or invasion, of melanoma cells through MAPK activation.
AB - The air-liquid interface (ALI) is a common microenvironment of the skin, but it is unknown whether the ALI affects melanoma cell behaviors. Using a collagen gel invasion assay, immuno histochemistry, and Western blots, here we show that melanoma cell proliferation in cultures with an ALI is higher than melanoma cell proliferation in submerged cultures. Bromodeoxyuridine (BrdU) uptake, an indicator of cell proliferation, of melanoma cells at the ALI was about 3 times that of submerged cells, while ALI and submerged melanoma cells had similar levels of single-stranded DNA (a marker of apoptosis). The ALI enhanced the expression of Raf-1, MEK-1 and pERK-1/2 components of the mitogen-activated protein kinase (MAPK) cascade, in cells more than the submerged condition did. The increases in BrdU uptake and pERK-1/2 expression promoted by ALI was abolished by the MEK inhibitor, PD-98059. ALI-treated and submerged melanoma cells did not infiltrate into the collagen gel, and they showed no significant difference in the expression of the invasion and motility-related molecules, matrix metalloproteinase-1 and -9, laminin 5, and filamin A. Our data indicate that the ALI, a skin microenvironment, accelerates the growth, but not the apoptosis or invasion, of melanoma cells through MAPK activation.
KW - Air-liquid interface
KW - Collagen gel invasion assay
KW - Melanoma
KW - Mitogen-activated protein kinase
KW - Proliferation
UR - https://www.scopus.com/pages/publications/77950836644
UR - https://www.scopus.com/inward/citedby.url?scp=77950836644&partnerID=8YFLogxK
U2 - 10.1267/ahc.09036
DO - 10.1267/ahc.09036
M3 - Article
AN - SCOPUS:77950836644
SN - 0044-5991
VL - 43
SP - 1
EP - 7
JO - Acta Histochemica et Cytochemica
JF - Acta Histochemica et Cytochemica
IS - 1
ER -