Translational IVF research

Within this line of research, the 'Reproductive Medicine Research Group' focuses on the development of novel diagnostic tools and alternative treatment options for patients experiencing failed ART. Research is always conducted under the supervision of Prof. Björn Heindryckx and Dr. Annekatrien Boel (post-doc).

Research projects

Failed fertilization with intracytoplasmic sperm injection (ICSI)

Injecting the sperm into the egg leads, in the majority of cases, to fertilization and the development of an embryo. Still, there is a population of patients who have repeated failed fertilization after this intracytoplasmic sperm injection (ICSI). Furthermore, it is also possible that the embryo development during the first division stages is repeatedly compromised. We investigate the molecular mechanisms underlying these problems and to identify the underlying genetic causes. 

For instance, we have developed a diagnostic test in mouse, by which we assess the oocyte-activating capacity of human sperm cells, after ICSI in mouse oocytes (mouse oocyte activation test – MOAT). Furthermore, we can also more specifically evaluate the calcium pattern, induced by sperm cells, after ICSI in mouse (mouse oocyte calcium analysis – MOCA), or human (human oocyte calcium analysis – HOCA) oocytes.

The Department for Reproductive Medicine has obtained worldwide expertise in the treatment of this specific patient population, overcoming failed fertilization, by evoking artificial calcium rises (assisted oocyte activation – AOA). With this AOA technique, most couples experiencing failed fertilization after ICSI significantly increase their chances to obtain a genetically related child.

  • researcher: Arantxa Cardona Barberán
  • funding: Funding for doctoral research of AAP (assisting academic staff), Ghent University

 

Study of early embryo developmental processes

Genes that contribute to the early development of mouse and human embryos have recently become easier to study by targeted gene disruption via the genome-modifying technique CRISPR/Cas. Also, the disruption of genes that play a crucial role in later developmental stages, such as embryo differentiation, implantation and stem cell derivation, is being investigated.

 

Mitochondrial disorders

Mitochondrial disorders, caused by mitochondrial DNA mutations, which are always inherited from mother to child, can be prevented by either pre-implantation genetic testing (PGT) or nuclear transfer. This nuclear transfer procedure involves the transfer of the nucleus from the mother's egg to a healthy donor egg, containing healthy mitochondrial DNA. In the general press, this technique is also called the "three-parent baby". 

Different nuclear transfer technologies are currently being evaluated both in mouse and human, amongst which spindle transfer and nuclear transfer (see figure) are the most well-known.

Nuclear Transfer

In addition to investigating nuclear transfer in the context of overcoming mitochondrial disorders, we also want to generate proof that the technique is valuable to overcome certain forms of female infertility, such as failed fertilization after ICSI-AOA, embryo developmental arrest and a limited ovarian reserve. For these women, oocyte donation is currently the only treatment option.

By using both mouse models as well as human cases, we aim to indicate which forms of female infertility could potentially benefit from this novel nuclear transfer technique.

 

Germline mutation correction

With the genome-editing technique CRISPR/Cas, it is possible to correct genetic mutations during fertilization. Our research is currently focused on the correction of mutations that lead to infertility, to prevent that babies, born after certain fertility treatments, will also suffer from infertility.

Collaborations

Publications

Questions?

  • Björn Heindryckx, principal investigator

+32 9 332 47 48

  • Annekatrien Boel, postdoctoral researcher

+32 9 332 52 76