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Publication : LXR and ABCA1 control cholesterol homeostasis in the proximal mouse epididymis in a cell-specific manner.

First Author  Ouvrier A Year  2009
Journal  J Lipid Res Volume  50
Issue  9 Pages  1766-75
PubMed ID  19395734 Mgi Jnum  J:153781
Mgi Id  MGI:4366224 Doi  10.1194/jlr.M800657-JLR200
Citation  Ouvrier A, et al. (2009) LXR and ABCA1 control cholesterol homeostasis in the proximal mouse epididymis in a cell specific manner. J Lipid Res 50:1766-1775
abstractText  Mammalian spermatozoa undergo important plasma membrane maturation steps during epididymal transit. Among these, changes in lipids and cholesterol are of particular interest as they are necessary for fertilization. However, molecular mechanisms regulating these transformations inside the epididymis are still poorly understood. Liver X receptors (LXR), the nuclear receptors for oxysterols, are of major importance in intracellular cholesterol homeostasis, and LXR-/- deficient male mice have already been shown to have reduced fertility at an age of 5 months, and complete sterility for nine month-old animals. This sterility phenotype is associated with testes and caput epididymides epithelial defects. The research presented in this paper was aimed at investigating how LXR act in the male caput epididymidis by analyzing key actors in cholesterol homeostasis. We show that accumulation of cholesteryl esters in LXR-/- male mice is associated with a specific loss of ABCA1 and an increase in apoptosis of apical cells of the proximal caput epididymidis. ABCG1 and SR-B1, two other cholesterol transporters, show little if any modifications. Our study also revealed that SR-B1 appears to have a peculiar expression pattern along the epididymal duct. These results should help in understanding the functional roles of LXR in cholesterol trafficking processes in caput epididymidis.
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