Infertility in Fabry's Disease: role of hypoxia and inflammation in determining testicular damage.

Fabry’s disease cellular and molecular rehabilitation hypoxia inflammation new therapeutic targets for infertility rehabilitation testicular damage

Journal

Frontiers in endocrinology
ISSN: 1664-2392
Titre abrégé: Front Endocrinol (Lausanne)
Pays: Switzerland
ID NLM: 101555782

Informations de publication

Date de publication:
2024
Historique:
received: 17 11 2023
accepted: 12 02 2024
medline: 8 3 2024
pubmed: 8 3 2024
entrez: 8 3 2024
Statut: epublish

Résumé

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 α-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. 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-1α and NFκB was analyzed by immunofluorescence (IF) and RT-PCR on homogeneous tissue fractions after laser capture microdissection (LCMD). 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-1α in stromal cells but not in seminiferous tubules. On the contrary, NFκB 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-1α/NFκB inflammatory-like pathway. 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-1α/NFκB expression and localization while activating HIF-1α/NFκB driven-inflammation-like response damaging seminiferous tubular epithelium and Sertoli's cells.

Identifiants

pubmed: 38455658
doi: 10.3389/fendo.2024.1340188
pmc: PMC10917934
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1340188

Informations de copyright

Copyright © 2024 Sansone, Barreca, Belli, Aventaggiato, Russo, Perrone, Russo, Tafani and Frustaci.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The author(s) declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Auteurs

Luigi Sansone (L)

Laboratory of Cellular and Molecular Pathology, IRCCS San Raffaele, Rome, Italy.
Department of Human Sciences and Promotion of the Quality of Life, San Raffaele Roma Open University, Rome, Italy.

Federica Barreca (F)

Laboratory of Cellular and Molecular Pathology, Department of Experimental Medicine, Sapienza University, Rome, Italy.

Manuel Belli (M)

Laboratory of Cellular and Molecular Pathology, IRCCS San Raffaele, Rome, Italy.
Department of Human Sciences and Promotion of the Quality of Life, San Raffaele Roma Open University, Rome, Italy.

Michele Aventaggiato (M)

Laboratory of Cellular and Molecular Pathology, Department of Experimental Medicine, Sapienza University, Rome, Italy.

Andrea Russo (A)

Department of Pathologic Anatomy, IRCCS Regina Elena, Rome, Italy.

Giulietta A Perrone (GA)

UOC of Pathologic Anatomy, San Filippo Neri Hospital, Rome, Italy.

Matteo A Russo (MA)

Laboratory of Cellular and Molecular Pathology, IRCCS San Raffaele, Rome, Italy.

Marco Tafani (M)

Laboratory of Cellular and Molecular Pathology, Department of Experimental Medicine, Sapienza University, Rome, Italy.

Andrea Frustaci (A)

Laboratory of Cellular and Molecular Pathology, IRCCS San Raffaele, Rome, Italy.

Classifications MeSH