Microfluidic versus molecular assays - different approaches in assessing oocyte developmental competence

J Biol Regul Homeost Agents. 2016 Jul-Sep;30(3):635-640.

Abstract

In recent years, molecular techniques have brought about new solutions that focus on the developmental capacity of female oocytes and reproductive performance in the mammalian species. The developmental potency is the ability of oocytes to reach the MII stage following the long stages of folliculo- and oogenesis. The main proteins involved in this process belong to the connexin (Cx) family, which are responsible for the formation of gap junction (GJC) connections between the female gamete and surrounding somatic cells. The Cx are involved in bi-directional transport of small molecules and are therefore responsible for correct oocyte-somatic cell nutrition, proliferation, and differentiation. However, the application of certain molecular techniques often leads to destabilization or destruction of the materials of interest, such as cells or whole tissues. Therefore, the applications of microfluidic methods, which are non-invasive and quantitative, give new opportunities to further this area of biomedical research. Microfluidic research is based on real-time experiments that allow for control and/ or observation of the results during each step. The purpose of this review is to present both positive and negative aspects of molecular-microfluidic methods while describing the role of connexins in oocyte developmental capacity.

Publication types

  • Review

MeSH terms

  • Animals
  • Biological Transport
  • Cell Communication
  • Cells, Cultured
  • Connexins / analysis*
  • Connexins / genetics
  • Connexins / physiology
  • Culture Media
  • Cumulus Cells / chemistry
  • Cumulus Cells / physiology
  • Female
  • Gap Junctions
  • Gene Expression Regulation, Developmental
  • Lab-On-A-Chip Devices
  • Mammals / physiology
  • Microfluidic Analytical Techniques*
  • Molecular Biology / methods
  • Oocytes / chemistry*
  • Oocytes / physiology
  • Oogenesis*
  • RNA, Messenger / analysis

Substances

  • Connexins
  • Culture Media
  • RNA, Messenger