Disruption of androgen signaling during puberty affects Notch pathway in rat seminiferous epithelium

Autor: Laura Pardyak, Sylwia Marek, Malgorzata Brzoskwinia, Barbara Bilińska, Anna Hejmej, Alicja Kamińska, P. Pawlicki
Rok vydání: 2020
Předmět:
Male
0301 basic medicine
puberty
medicine.medical_treatment
Gene Expression
Flutamide
chemistry.chemical_compound
0302 clinical medicine
Endocrinology
Testis
Basic Helix-Loop-Helix Transcription Factors
lcsh:Reproduction
Testosterone
Sexual Maturation
Notch signaling
Receptors
Notch

Obstetrics and Gynecology
Seminiferous Epithelium
Receptors
Androgen

030220 oncology & carcinogenesis
Androgens
Signal Transduction
medicine.medical_specialty
JAG1
lcsh:QH471-489
medicine.drug_class
Notch signaling pathway
testis
Biology
lcsh:Gynecology and obstetrics
03 medical and health sciences
Internal medicine
medicine
Animals
Humans
Rats
Wistar

lcsh:RG1-991
Research
Puberty
androgens
Androgen Antagonists
Androgen
Repressor Proteins
Androgen receptor
Steroid hormone
030104 developmental biology
Reproductive Medicine
chemistry
Transcription Factor HES-1
Spermatogenesis
Jagged-1 Protein
Developmental Biology
Zdroj: Reproductive Biology and Endocrinology, Vol 18, Iss 1, Pp 1-14 (2020)
Reproductive Biology and Endocrinology : RB&E
ISSN: 1477-7827
DOI: 10.1186/s12958-020-00582-3
Popis: Background Onset of spermatogenesis at puberty is critically dependent on the activity of hypothalamic-pituitary-gonadal axis and testosterone production by Leydig cells. The aim of this study was to examine whether activation of Notch receptors and expression of Notch ligands and effector genes in rat seminiferous epithelium are controlled by androgen signaling during puberty. Methods Peripubertal (5-week-old) Wistar rats received injections of flutamide (50 mg/kg bw) daily for 7 days to reduce androgen receptor (AR) signaling or a single injection of ethanedimethane sulphonate (EDS; 75 mg/kg bw) to reduce testosterone production. Gene and protein expressions were analyzed by real-time RT-PCR and western blotting, respectively, protein distribution by immunohistochemistry, and steroid hormone concentrations by enzyme-linked immunosorbent assay. Statistical analyses were performed using one-way ANOVA followed by Tukey’s post hoc test or by Kruskal-Wallis test, followed by Dunn’s test. Results In both experimental models changes of a similar nature in the expression of Notch pathway components were found. Androgen deprivation caused the reduction of mRNA and protein expression of DLL4 ligand, activated forms of Notch1 and Notch2 receptors and HES1 and HEY1 effector genes (p p p p p p Conclusions Androgens and androgen receptor signaling may be considered as factors regulating Notch pathway activity and the expression of Hes and Hey genes in rat seminiferous epithelium during pubertal development. Further studies should focus on functional significance of androgen-Notch signaling cross-talk in the initiation and maintenance of spermatogenesis.
Databáze: OpenAIRE