Cargando…

Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia

Mechanisms underlying severe male infertility are still largely elusive. However, recently, a single-cell transcription study by our group identified several differentially expressed coding genes in all the somatic cell types in testes of patients with idiopathic germ cell aplasia (iGCA). Here, we l...

Descripción completa

Detalles Bibliográficos
Autores principales: Lavorgna, Giovanni, Tascini, Anna Sofia, Bertini, Alessandro, Lanzaro, Francesco, Montorsi, Francesco, Alfano, Massimo, Salonia, Andrea
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486010/
https://www.ncbi.nlm.nih.gov/pubmed/36147743
http://dx.doi.org/10.3389/fcell.2022.952518
_version_ 1784792183789846528
author Lavorgna, Giovanni
Tascini, Anna Sofia
Bertini, Alessandro
Lanzaro, Francesco
Montorsi, Francesco
Alfano, Massimo
Salonia, Andrea
author_facet Lavorgna, Giovanni
Tascini, Anna Sofia
Bertini, Alessandro
Lanzaro, Francesco
Montorsi, Francesco
Alfano, Massimo
Salonia, Andrea
author_sort Lavorgna, Giovanni
collection PubMed
description Mechanisms underlying severe male infertility are still largely elusive. However, recently, a single-cell transcription study by our group identified several differentially expressed coding genes in all the somatic cell types in testes of patients with idiopathic germ cell aplasia (iGCA). Here, we leverage this work by extending the analysis also to the non-coding portion of the genome. As a result, we found that 43 LncRNAs were differentially expressed in the somatic cells of these patients. Interestingly, a significant portion of the overexpressed LncRNAs was found to be a target of TAF9B, a transcription factor known to be involved in germ cell survival. Moreover, several overexpressed LncRNAs were also found to be activated in a mouse model of Sertoli cells treated with bisphenol A, a widespread environmental contaminant, long suspected to impair male fertility. Finally, a literature search for MEG3, a maternally imprinted LncRNA overexpressed as well in our patients, found it to be involved, among other things, in obesity and inflammation, known comorbidities of iGCA, ultimately suggesting that our findings deepen the understanding of the molecular insights coupled not only to the pathogenesis, but also to the clinical course of this class of patients.
format Online
Article
Text
id pubmed-9486010
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-94860102022-09-21 Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia Lavorgna, Giovanni Tascini, Anna Sofia Bertini, Alessandro Lanzaro, Francesco Montorsi, Francesco Alfano, Massimo Salonia, Andrea Front Cell Dev Biol Cell and Developmental Biology Mechanisms underlying severe male infertility are still largely elusive. However, recently, a single-cell transcription study by our group identified several differentially expressed coding genes in all the somatic cell types in testes of patients with idiopathic germ cell aplasia (iGCA). Here, we leverage this work by extending the analysis also to the non-coding portion of the genome. As a result, we found that 43 LncRNAs were differentially expressed in the somatic cells of these patients. Interestingly, a significant portion of the overexpressed LncRNAs was found to be a target of TAF9B, a transcription factor known to be involved in germ cell survival. Moreover, several overexpressed LncRNAs were also found to be activated in a mouse model of Sertoli cells treated with bisphenol A, a widespread environmental contaminant, long suspected to impair male fertility. Finally, a literature search for MEG3, a maternally imprinted LncRNA overexpressed as well in our patients, found it to be involved, among other things, in obesity and inflammation, known comorbidities of iGCA, ultimately suggesting that our findings deepen the understanding of the molecular insights coupled not only to the pathogenesis, but also to the clinical course of this class of patients. Frontiers Media S.A. 2022-09-06 /pmc/articles/PMC9486010/ /pubmed/36147743 http://dx.doi.org/10.3389/fcell.2022.952518 Text en Copyright © 2022 Lavorgna, Tascini, Bertini, Lanzaro, Montorsi, Alfano and Salonia. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cell and Developmental Biology
Lavorgna, Giovanni
Tascini, Anna Sofia
Bertini, Alessandro
Lanzaro, Francesco
Montorsi, Francesco
Alfano, Massimo
Salonia, Andrea
Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia
title Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia
title_full Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia
title_fullStr Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia
title_full_unstemmed Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia
title_short Single-cell transcriptome profiling reveals several LncRNAs differentially expressed in idiopathic germ cell aplasia
title_sort single-cell transcriptome profiling reveals several lncrnas differentially expressed in idiopathic germ cell aplasia
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9486010/
https://www.ncbi.nlm.nih.gov/pubmed/36147743
http://dx.doi.org/10.3389/fcell.2022.952518
work_keys_str_mv AT lavorgnagiovanni singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia
AT tasciniannasofia singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia
AT bertinialessandro singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia
AT lanzarofrancesco singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia
AT montorsifrancesco singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia
AT alfanomassimo singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia
AT saloniaandrea singlecelltranscriptomeprofilingrevealsseverallncrnasdifferentiallyexpressedinidiopathicgermcellaplasia