Localization of EFA6 (exchange factor for ARF6) isoform D in steroidogenic testicular Leydig cells of adult mice

被引:0
作者
Chomphoo, Surang [1 ]
Pakkarato, Sawetree [2 ]
Sawatpanich, Tarinee [1 ]
Sakagami, Hiroyuki [3 ]
Kondo, Hisatake [1 ]
Hipkaeo, Wiphawi [1 ]
机构
[1] Khon Kaen Univ, Electron Microscopy Unit, Fac Med, Dept Anat, Khon Kaen 40002, Thailand
[2] Rajamangala Univ Technol Isan, Fac Sci & Liberal Arts, Dept Social Sci, Sura Narai Rd, Nai Muang Muang 30000, Nakhon Ratchasi, Thailand
[3] Kitasato Univ, Sch Med, Dept Anat, Tokyo, Japan
关键词
EFA6D; Ultrastructural localization; Membrane trafficking; Leydig cells; RIBOSYLATION FACTOR 6; SUBCELLULAR-LOCALIZATION; RECEPTOR DESENSITIZATION; PLASMA-MEMBRANE; MOUSE-BRAIN; FAMILY; ACTIVATION; TRANSPORT; PROTEINS; ROLES;
D O I
10.1016/j.acthis.2018.02.009
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
EFA6 (exchange factor for ARF6) activates Arf6 (ADP ribosylation factor 6) by exchanging ADP to ATP and the resulting activated form of Arf6 is involved in the membrane trafficking and actin remodeling of cells. Our previous study has shown the selective expression/localization of EFA6D in steroidogenic adrenocortical cells in situ of adult mice. In view of the previous finding, the present study was undertaken to examine its localization in mouse Leydig cells representing another steroidogenic cell species in order to further support the possible involvement of the EFA6/Arf6 cascade via membrane trafficking in the regulation of steroidogenesis and/or secretion. A distinct band for EFA6D with the same size as that of the brain was detected in the testis of adult mice. In immuno-light microscopy, immunoreactivity for EFA6D was seen throughout the cytoplasm in most Leydig cells without any distinct accumulation along the plasmalemma. Lack of immunoreactivity for EFA6D was seen in the seminiferous tubular epithelium. In immuno-electron microscopy, the immune-labeling was seen in sporadic/focal patterns on plasma membranes and some vesicles and vacuoles subjacent to the plasma membranes. More constant and rather predominant is the labeling on numerous mitochondria. No immuno-labeling was seen in lipid droplets. The present study suggests that EFA6D is somehow involved in regulation of the synthesis and/or secretion of testosterone through the membrane-traffic by activation of Arf6. In addition, EFA6D is suggested to play in mitochondria some yet unidentified roles rather independent of Arf6-activation, which remains to be elucidated.
引用
收藏
页码:263 / 268
页数:6
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