Comparison of colony formation of human spermatogonial stem cells (SSCs) with and without collagen

J Pak Med Assoc. 2016 Mar;66(3):285-91.

Abstract

Objective: To investigate the effects of collagen and growth factors on in vitro proliferation of human spermatogonial stem cells obtained from patients with non-obstructive azoospermia.

Methods: The experimental cross-sectional study was conducted from February 2013 to April 2015 after obtaining approval from the ethics committee of Ahvaz Jundishapur University of Medical Sciences, Iran. Testicular sperm extractions of non-obstructive azoospermic patients were obtained from the Clinical Urology and Embryology, In Vitro Fertilization Department of Imam Khomeini Hospital. Spermatogonial stem cells and Sertoli cells, obtained from human testis biopsies by a two-step enzymatic digestion method, were purified using fluorescence- activated cell-sorting and daturastramonium-lectin, and were cultured separately. To investigate a more direct influential factor on colony formation, one control and two experimental groups were formed. Group 1 acted as the control in which spermatogonial stem cells were co-cultured with Sertoli cells alone. In group 2 they were co-cultured with Sertoli cells and growth factors such as leukaemia inhibitory factor, epidermal growth factor and glial cell-derived neurotrophic factor, and in group 3 with Sertoli cells along with growth factors in the presence of collagen-coated dishes. Number and diameter of the colonies were evaluated after 7 weeks.

Results: Specimens obtained related to 21 patients. Number and diameter of the colonies in group 3 (18±2.6 and 276.6±45.5) were significantly more than both groups 1 (3.5±1 and D1:81.6±12) and group 2(11±2.2 and 165.2±32.5) (p<0.05 each). Also, the number and diameter of colony in group 2 were significantly better than the control group (p<0.05).Expression profile of the VASA, promyelocytic leukaemia zinc-finger (PLZF), Octamer-binding transcription factor 4 (OCT4) and integrin a6 (INTGa6) were detected in all groups. Based on cytochemical findings, OCT4 was expressed in the colonies of all three groups.

Conclusions: According to positive effects of collagen and growth factors on the colonisation of spermatogonial stem cells, it seems that using the cells may lead to better colonisation of this type of stem cells.

Keywords: Spermatogonial stem cells, SSCs, Growth factor, Collagen, Co-culture..

Publication types

  • Comparative Study

MeSH terms

  • Adult Germline Stem Cells / cytology
  • Adult Germline Stem Cells / drug effects*
  • Azoospermia
  • Cell Culture Techniques
  • Cell Proliferation / drug effects*
  • Coculture Techniques
  • Collagen / pharmacology*
  • Cross-Sectional Studies
  • DEAD-box RNA Helicases / drug effects
  • DEAD-box RNA Helicases / metabolism
  • Epidermal Growth Factor / pharmacology
  • Flow Cytometry
  • Glial Cell Line-Derived Neurotrophic Factor / pharmacology
  • Humans
  • Integrin alpha6 / drug effects
  • Integrin alpha6 / metabolism
  • Kruppel-Like Transcription Factors / drug effects
  • Kruppel-Like Transcription Factors / metabolism
  • Leukemia Inhibitory Factor / pharmacology
  • Male
  • Octamer Transcription Factor-3 / drug effects
  • Octamer Transcription Factor-3 / metabolism
  • Promyelocytic Leukemia Zinc Finger Protein
  • Sertoli Cells

Substances

  • Glial Cell Line-Derived Neurotrophic Factor
  • Integrin alpha6
  • Kruppel-Like Transcription Factors
  • Leukemia Inhibitory Factor
  • Octamer Transcription Factor-3
  • Promyelocytic Leukemia Zinc Finger Protein
  • ZBTB16 protein, human
  • Epidermal Growth Factor
  • Collagen
  • DDX4 protein, human
  • DEAD-box RNA Helicases

Supplementary concepts

  • Azoospermia, Nonobstructive