Infertility in Fabry's Disease: role of hypoxia and inflammation in determining testicular damage
被引:2
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作者:
Sansone, Luigi
论文数: 0引用数: 0
h-index: 0
机构:
IRCCS San Raffaele, Lab Cellular & Mol Pathol, Rome, Italy
San Raffaele Roma Open Univ, Dept Human Sci & Promot Qual Life, Rome, ItalyIRCCS San Raffaele, Lab Cellular & Mol Pathol, Rome, Italy
机构:
IRCCS San Raffaele, Lab Cellular & Mol Pathol, Rome, Italy
San Raffaele Roma Open Univ, Dept Human Sci & Promot Qual Life, Rome, ItalyIRCCS San Raffaele, Lab Cellular & Mol Pathol, Rome, Italy
[4] IRCCS Regina Elena, Dept Pathol Anat, Rome, Italy
[5] San Filippo Neri Hosp, UOC Pathol Anat, Rome, Italy
来源:
FRONTIERS IN ENDOCRINOLOGY
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2024年
/
15卷
关键词:
Fabry's disease;
hypoxia;
inflammation;
cellular and molecular rehabilitation;
testicular damage;
new therapeutic targets for infertility rehabilitation;
NF-KAPPA-B;
GLOBOTRIAOSYLCERAMIDE;
INVOLVEMENT;
EXPRESSION;
TARGET;
VEGF;
D O I:
10.3389/fendo.2024.1340188
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Introduction Fabry's disease (FD) is a genetic X-linked systemic and progressive rare disease characterized by the accumulation of globotriaosylceramide (GB3) into the lysosomes of many tissues. FD is due to loss-of-function mutations of alpha-galactosidase, a key-enzyme for lysosomal catabolism of glycosphingolipids, which accumulate as glycolipid bodies (GB). In homozygous males the progressive deposition of GB3 into the cells leads to clinical symptoms in CNS, skin, kidney, etc. In testis GB accumulation causes infertility and alterations of spermatogenesis. However, the precise damaging mechanism is still unknown. Our hypothesis is that GB accumulation reduces blood vessel lumen and increases the distance of vessels from both stromal cells and seminiferous parenchyma; this, in turn, impairs oxygen and nutrients diffusion leading to subcellular degradation of seminiferous epithelium and sterility.Methods To test this hypothesis, we have studied a 42-year-old patient presenting a severe FD and infertility, with reduced number of spermatozoa, but preserved sexual activity. Testicular biopsies were analyzed by optical (OM) and transmission electron microscopy (TEM). Activation and cellular localization of HIF-1 alpha and NF kappa B was analyzed by immunofluorescence (IF) and RT-PCR on homogeneous tissue fractions after laser capture microdissection (LCMD).Results OM and TEM showed that GB were abundant in vessel wall cells and in interstitial cells. By contrast, GB were absent in seminiferous epithelium, Sertoli's and Leydig's cells. However, seminiferous tubular epithelium and Sertoli's cells showed reduced diameter, thickening of basement membrane and tunica propria, and swollen or degenerated spermatogonia. IF showed an accumulation of HIF-1 alpha in stromal cells but not in seminiferous tubules. On the contrary, NF kappa B fluorescence was evident in tubules, but very low in interstitial cells. Finally, RT-PCR analysis on LCMD fractions showed the expression of pro-inflammatory genes connected to the HIF-1 alpha/NF kappa B inflammatory-like pathway.Conclusion Our study demonstrates that infertility in FD may be caused by reduced oxygen and nutrients due to GB accumulation in blood vessels cells. Reduced oxygen and nutrients alter HIF-1 alpha/NF kappa B expression and localization while activating HIF-1 alpha/NF kappa B driven-inflammation-like response damaging seminiferous tubular epithelium and Sertoli's cells.