Sertoli cells from non-obstructive azoospermia and obstructive azoospermia patients show distinct morphology, Raman spectrum and biochemical phenotype.

نویسندگان

  • Meng Ma
  • Shi Yang
  • Zhenzhen Zhang
  • Peng Li
  • Yuehua Gong
  • Linhong Liu
  • Yong Zhu
  • Ruhui Tian
  • Yufei Liu
  • Xiaobo Wang
  • Feng Liu
  • Lin He
  • Yang Liu
  • Hao Yang
  • Zheng Li
  • Zuping He
چکیده

STUDY QUESTION Are there differences in the morphology, spectrum and biochemical phenotype between Sertoli cells from non-obstructive azoospermia (NOA) patients and those from obstructive azoospermia (OA) patients with normal spermatogenesis? SUMMARY ANSWER Sertoli cells from NOA patients are distinct from those from OA patients in terms of morphological features, Raman spectrum and phenotype including the expression of genes and proteins (e.g. SCF, BMP4 and GDNF). WHAT IS KNOWN ALREADY NOA affects 10% of infertile men and has been diagnosed in 60% of azoospermic men. In contrast with OA patients who have normal spermatogenesis, NOA patients have an impaired spermatogenesis. STUDY DESIGN, SIZE AND DURATION This case-control study included 100 NOA patients (as cases) and 100 OA patients with normal spermatogenesis (as controls). The study was performed between January 2012 and January 2013. PARTICIPANTS/MATERIALS, SETTING AND METHODS Karyotype analysis was performed to check the chromosome content and multiplex PCR was carried out to determine the expression of numerous Y chromosome genes in NOA patients. Human Sertoli cells were then isolated from the testes of NOA and OA patients by two-step enzymatic digestion and differential plating. Transmission electron microscopy was used to determine the ultrastructure of the Sertoli cells and real-time Raman microspectroscopy was used to assess their spectrum. We further compared the two groups of patients for expression of SCF, GDNF and BMP4 in Sertoli cells, using RT-PCR, microarray analysis, immunofluorescence, immunohistochemistry and Western blots. MAIN RESULTS AND THE ROLE OF CHANCE NOA patients had normal chromosome karyotypes and Y chromosome microdeletions were excluded. In morphology, Sertoli cells isolated from NOA patients had a series of abnormal ultrastructural features compared with the control Sertoli cells: (i) existence of small and spindle-shaped nuclei, (ii) smaller diameter, (iii) deficient nucleolus or endoplasmic reticulum and (iv) more vacuoles. Spectral intensities in Sertoli cells of NOA patients were distinct at four typical Raman peaks compared with the control Sertoli cells. In phenotype, SCF, BMP4 and GDNF transcripts and proteins were significantly lower in Sertoli cells of NOA patients than in the control Sertoli cells. LIMITATIONS AND REASONS FOR CAUTION The Sertoli cells of NOA patients were not compared with Sertoli cells of normal fertile men due to the fact that it is hard to obtain adult testes from normal donors. WIDER IMPLICATIONS OF THE FINDINGS This study provides novel insights into understanding the underlying causes for NOA and might offer a basis for developing new therapeutic strategies for patients with NOA.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

P-231: Androgen Receptor Gene Expression in Azoospermia Men

Background: Androgens are critical steroid hormones in progression of spermatogenesis process and determine the male phenotype that their actions are mediated by the androgen receptor (AR), a member of the nuclear receptor superfamily. In the Androgen receptor, transactivation domain encoded by exon 1, DNA binding domain encoded by exons 2 and 3, hinge region encoded by part of exon 4, and C-te...

متن کامل

Absence of anti-Müllerian hormone (AMH) and M2A immunoreactivities in Sertoli cell-only syndrome and maturation arrest with and without AZF microdeletions.

BACKGROUND Some genes identified in the AZF locus are expressed only in germinal cells; others are ubiquitous. AZF microdeletions seem to occur at the earliest stages of ontogenetic development, and one might therefore assume that Sertoli cells preserve some immature characteristics and that their immunophenotype may be modified by the existence of a molecular defect. MATERIALS AND METHODS Tw...

متن کامل

P-40: Characteristics of Gonadotrophins in Azoospermic Patients in Plateau State, Nigeria

Background: Azoospermia is the total absence of sperm cells from a patients semen sample after centrifugation. It could be obstructive or non-obstructive and its associated causes include chromosomal defects, infections, gonadotrophins imbalance, and etc in the patients. The objective is to determine the prevalence of primary testicular failure, germinal insufficiency, obstructive azoospermia a...

متن کامل

P-232: Gene Expression Analysis of the Histon Variant H2BFWT in Testis Tissues of Non-Obstructive Azoospermic Patients Referred to Royan Institute

Background: During the later stages of spermatogenesis, spermatid nuclear remodeling and condensation are associated with histone modifications and the sequential displacement of histones by transition proteins and then by protamines. In humans, approximately 15% of the sperm DNA remains packaged by histones in sequence-specific areas. The histone variant H2B, member W, testis-specific (H2BFWT)...

متن کامل

O-40: MTHFR Promoter Hypermethylationin Testicular Biopsies of patients with Non-Azoospermia: the Role of Epigeneticsin Male Infertility

Background: MTHFR promoter hypermethylation in testicular biopsies of patients with non-obstructive azoospermia: the role of epigenetics in male infertility. Materials and Methods: DNA from peripheral blood (PB) samples of 50 patients with NOA and 50 fertile men (controls) as well as DNA from testicular biopsies of 32 patients with NOA and five patients with obstructive azoospemia, but normal s...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Human reproduction

دوره 28 7  شماره 

صفحات  -

تاریخ انتشار 2013