Abstract

BackgroundTo determine whether matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMP-1 and TIMP-2) in human follicular fluid, have any relationships with oocyte maturation in vivo and subsequent fertilization during in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) cycles.MethodsThe follicular fluids were obtained from 150 female patients undergoing IVF/ICSI cycles and a total of 1504 oocytes were retrieved for analysis. MMP-2 and MMP-9 activities were measured using zymography assay. TIMP-1 and TIMP-2 concentrations were quantitatively assessed using enzyme-linked immunosorbent assay (ELISA).ResultsHuman follicular fluid MMP-2 level was significantly associated with the rate of maturity of oocytes (P < 0.001). Furthermore, the MMP-2 was significantly associated with the higher fertilization rate (P < 0.01). There was no significant correlation between follicular MMP-9 and the maturation rate of oocytes. The TIMP-1 and TIMP-2 also showed no correlation with the oocyte maturation rate.ConclusionsThe level of gelatinase MMP-2 in human follicular fluid might be a reliable marker of mature oocytes during IVF/ICSI cycles. Furthermore, the MMP-2 expression has a strong association with higher fertilization rate. Further studies are needed to support this theory.

Highlights

  • To determine whether matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMP-1 and tissue inhibitors of metalloproteinases (TIMPs)-2) in human follicular fluid, have any relationships with oocyte maturation in vivo and subsequent fertilization during in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) cycles

  • Matrix metalloproteinase-2 (MMP-2) and matrix metalloproteinase-9 (MMP-9) belong to gelatinases and their activities are inhibited by tissue inhibitors of metalloproteinases (TIMPs)

  • We proposed that the MMP-2 is a reliable factor associated with oocyte maturation in IVF/ICSI cycles

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Summary

Introduction

To determine whether matrix metalloproteinases (MMPs) and their tissue inhibitors (TIMP-1 and TIMP-2) in human follicular fluid, have any relationships with oocyte maturation in vivo and subsequent fertilization during in vitro fertilization (IVF) or intracytoplasmic sperm injection (ICSI) cycles. During an assisted reproductive technology cycle, human pregnancy is dependent on a number of physiologic conditions, including oocyte maturation, successful fertilization, and embryonic blastocyst development [1, 2]. The clinical prediction of oocyte maturation in in vitro fertilization (IVF) / intracytoplasmic sperm injection (ICSI) cycles mainly depend on the size of leading follicles (>17 mm in diameter) and are sometimes accompanied by serum estradiol level. MMP and TIMP proteins have been detected in the sperm-oocyte interaction.

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