TY - JOUR
T1 - Importance of forkhead transcription factor Fkhl18 for development of testicular vasculature
AU - Sato, Yuko
AU - Baba, Takashi
AU - Zubair, Mohamad
AU - Miyabayashi, Kanako
AU - Toyama, Yoshiro
AU - Maekawa, Mamiko
AU - Owaki, Akiko
AU - Mizusaki, Hirofumi
AU - Sawamura, Tatsuya
AU - Toshimori, Kiyotaka
AU - Morohashi, Ken Ichirou
AU - Katoh-Fukui, Yuko
PY - 2008/9
Y1 - 2008/9
N2 - Forkhead transcription factors are characterized by a winged helix DNA binding domain, and the members of this family are classified into 20 subclasses by phylogenetic analyses. Fkhl18 is structurally unique, and is classified into FoxS subfamily. We found Fkhl18 expression in periendothelial cells of the developing mouse fetal testis. In an attempt to clarify its function, we generated mice with Fkhl18 gene disruption. Although KO mice developed normally and were fertile in both sexes, we frequently noticed unusual blood accumulation in the fetal testis. Electron microscopic analysis demonstrated frequent gaps, measuring 100-400 nm, in endothelial cells of blood vessels. These gaps probably represented ectopic apoptosis of testicular periendothelial cells, identified by caspase-3 expression, in KO fetuses. No apoptosis of endothelial cells was noted. Fkhl18 suppressed the transcriptional activity of FoxO3a and FoxO4. Considering that Fas ligand gene expression is activated by Foxs, the elevated activity of Foxs in the absence of Fkhl18 probably explains the marked apoptosis of periendothelial cells in Fkhl18 KO mice.
AB - Forkhead transcription factors are characterized by a winged helix DNA binding domain, and the members of this family are classified into 20 subclasses by phylogenetic analyses. Fkhl18 is structurally unique, and is classified into FoxS subfamily. We found Fkhl18 expression in periendothelial cells of the developing mouse fetal testis. In an attempt to clarify its function, we generated mice with Fkhl18 gene disruption. Although KO mice developed normally and were fertile in both sexes, we frequently noticed unusual blood accumulation in the fetal testis. Electron microscopic analysis demonstrated frequent gaps, measuring 100-400 nm, in endothelial cells of blood vessels. These gaps probably represented ectopic apoptosis of testicular periendothelial cells, identified by caspase-3 expression, in KO fetuses. No apoptosis of endothelial cells was noted. Fkhl18 suppressed the transcriptional activity of FoxO3a and FoxO4. Considering that Fas ligand gene expression is activated by Foxs, the elevated activity of Foxs in the absence of Fkhl18 probably explains the marked apoptosis of periendothelial cells in Fkhl18 KO mice.
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U2 - 10.1002/mrd.20888
DO - 10.1002/mrd.20888
M3 - Article
C2 - 18288644
AN - SCOPUS:47749103330
SN - 1040-452X
VL - 75
SP - 1361
EP - 1371
JO - Molecular Reproduction and Development
JF - Molecular Reproduction and Development
IS - 9
ER -