The first Open Innovation Lab research unit at IBEC will be Bioengineering in Reproductive Health @Biorephealth, led by Dr. Samuel Ojosnegros.
The main research focus of our lab is to study the development of human and mouse embryos. We combine bioengineering and optics tools to generate novel technologies that allow us to study the mechanisms controlling mammalian embryo implantation. Our proprietary solutions can be used to improve in vitro fertilization (IVF) and have been licensed by the pharma industry. The strong translational component of our research is not limited to embryology but convey into other disciplines such as diagnostics and cell therapies.
The development of the embryo E in humans (and mammals in general) requires the embryo to implantat, which proceeds with the attachment of the embryo into the walls of the mother uterus and invasion of the tissue to form the placenta. This process is crucial for natural conception and especially for in vitro fertilization (IVF) as only 30% of IVF embryos successfully implant into the mother uterus’ and develop to term. However, despite the importance of implantation in human fertility, this process is still elusive for experimentation because the uterus is rather inaccessible and difficult to be analysed
In our lab we create microscopes and bioengineered platforms to study the 3D environments that support embryonic development outside of the mother uterus. Our systems allow us to interrogation of the genetics, metabolomics and mechanics of the embryo in a high throughput manner. Using our systems, we are capable to (i) improve embryo culture conditions and (ii) diagnose embryos with improved implantation potential.
Our dual research philosophy with a basic-translational component, has granted us collaboration contracts with the pharma industry, hospitals, and venture capital to bring our technology to the clinics and to the market. Our innovative Open Lab is a multidisciplinary environment where biologists, biophysicists, clinicians, and business developers synergize to create a unique environment shaped by science and entrepreneurship.
Molecular mechanisms of embryo implantation
Human reproduction is surprisingly inefficient compared to other mammalian species. On average, 25–30% of natural conceptions lead to successful live births. IVF leads to a successful live birth only in about 30% of the times (averaged per embryo transferred). Around 60% of all conceptions are lost at the time of (or soon after) implantation. Implantation is not only a cornerstone of reproduction but an evolutionary novelty of mammals.
During implantation, the embryo at blastocyst stage attaches to the epithelial lining of the uterus (the endometrium). A specialized embryonic tissue, termed the trophoblast, invades the endometrium reaching out and connecting to the blood vessels. The trophoblast will give rise to the placenta and umbilical cord allowing continuous nutrient supply to the embryo and consequently a prolonged intrauterine retention of the embryo during pregnancy. However, the study of implantation is mainly inaccessible because it takes place inside the adult. To overcome this problem, we have developed proprietary culture methods and ex vivo implantation platforms which mimic the uterine microenvironment, allowing the embryo to progress towards post-implantation stages in an amenable way for optical microscopy.
Development of Human Plasma-Derived Protein Supplement to Improve Embryo Culture and Promote Embryo Implantation
Embryo culture in vitro from one cell stage to blastocyst stage in IVF clinics is carried out using human serum albumin (HSA). However non-clinical grade serums (such as FBS) have the potential to push the development of embryos further, but of course they cannot be used in the clinics. In the last years, in collaboration with GRIFOLS we have co-developed serums with batch consistency and clinical approval to culture human embryos. In addition to albumin these serums also provide growth factors, vitamins and other components that are removed during the purification process of albumin. This cocktail improves the efficiency of the development towards blastocyst stage and promote embryo ex vivo implantation.
Spectroscopy and label-free imaging
Spectroscopy refers to a family of imaging techniques which aim to extract information from the sample signal beyond the intensity profile. These techniques provide an additional dimension (i.e., spectral, oligomeric) to the image acquired.
Label-free microscopy, such as the imaging of autofluorescence signals from the cells, provide metabolic information of living tissues when analyzed using multispectral techniques.
In our lab we have specialized in spectroscopy imaging with emphasis on label-free methods. These methods are non-invasive, they do not require staining or sample manipulation whatsoever. For these reasons label-free imaging enables us to bring state-of-the-art microscopy techniques from the lab into the clinics, and study samples of biomedical relevance undisturbed at unprecedented level of detail.
Enhanced Number and Brightness a novel Imaging technique reveals protein dynamics in live cells
Proteins continuously interact with other proteins in the cell yet revealing these interactions in live-cell microscopy is technically challenging. Using statistical tools, we designed the Enhanced Number and Brightness method, which quantifies and maps protein aggregation in live cells in high resolution movies.
Several fluorescence microscopy methods are used to measure protein interactions in cells. However, most of these methods struggle to capture both the diversity of these interactions across the entire cellular area and their dynamics over time. To overcome these limitations, we enhanced the spatiotemporal resolution of Number and Brightness, a spectroscopy method that transforms fluorescence fluctuations into protein aggregation values.
The Enhanced Number and Brightness method implements two algorithms, the first one uses statistical tools to extract the distribution of protein oligomers (monomers, dimers, trimers and so on) in single pixels, thus revealing protein diversity across an entire cell image. The second one corrects the fluorescence intensity loss due to continuous light exposure, which enables measurements over prolonged periods of time. By combining these two algorithms, Enhanced Number and Brightness allows extended live imaging, providing dynamic maps of protein oligomerization overlaid on top of the corresponding cell image.
Figure: Enhanced Number and Brightness provides oligomerization maps (color-coded according to reference bar) during time-lapse movies. The image shows from left to right the dynamics of Eph receptor aggregation after stimulation with the ligand Ephrin. Each row depicts a cell stimulated with different types of ligands (i.e. soluble, surface-bound etc.).
|HSMe-ImPredict · Development of non-invasive imaging methodology for improving embryo implantation prediction, via hyper-spectral metabolic profiling (2022-2024)||Marie Curie Individual Fellowship||Samuel Ojosnegros|
|HYSPLANT · Selección de embriones para fecundación in vitro: predicción del éxito de implantación mediante clasificación metabólica de embriones (2020-2023)||MINECO|
Retos investigación: Proyectos I+D
|Prediction of implantation success by hyperspectral metabolic profiling of human embryos obtained by in vitro fertilization (2020-2022)||AGAUR|
Beatriu de Pinós 2018
|Estudio del mecanismo de acción de OXO-001 (2020-2022)||Oxolife||Samuel Ojosnegros|
|Evaluación de derivados plasmáticos humanos para el cultivo de embriones (2019-2021)||IVFTECH S.L.||Samuel Ojosnegros|
|Evaluación de derivados plasmáticos humanos para el cultivo de células mesenquimales y CAR-T (2020-2022)||IVFTECH S.L.||Samuel Ojosnegros|
|Prediction of implantation success by single-cell transcriptomic profiling of human embryos obtained by in vitro fertilization (2018-2022)||Scranton Enterprises BV||Samuel Ojosnegros|
|HYSPLANT · Metabolic profiling of in vitro fertilization embryos using hyspectral imaging (2019-2020)||European Commission ATTRACT||Samuel Ojosnegros|
|Embryo on a chip: Smart microdevice development for high-throughput screening embryo implantation (2020)||Tecniospring 2020||Maria Demestre Viladevall|
S Ojosnegros, A Seriola, AL Godeau, A Veiga (2021) Embryo implantation in the laboratory: an update on current techniques. Human Reproduction Update, Vol.00, No.0, pp. 1–30.
Martin Plöschner, Denitza Denkova, Simone De Camillis, Minakshi Das, Lindsay M. Parker, Xianlin Zheng, Yiqing Lu, Samuel Ojosnegros, and James A. Piper (2020) Simultaneous super-linear excitation-emission and emission depletion allows imaging of upconversion nanoparticles with higher sub-diffraction resolution. Optics Express 28 (16), 24308-24326.
- Micromanipulation-microinjection station
- Embryo biopsy laser
- Embryo culture laboratory
- Genome editing
- In vitro fertilization
- Cell culture laboratory
- 3D cell culture
- Advanced live imaging: photoconversion, 3D imaging, light scattering, spectroscopy
- Image analysis workstation
- Prof. Anna Veiga – Barcelona Stem Cell Bank (IDIBELL) and Dexeus Mujer, Barcelona
- Dr. Montserrat Boada/ Dr. Pere Barri – Dexeus Mujer, Barcelona
- Dr. Ayelet Lesman – Tel Aviv University (TAU), Israel
- Dr. Elena Martínez – IBEC
- Dr. Francesco Cutrale, University of Southern California (USC), USA
- Dr. Manuel Irimia – CRG, Barcelona
- Dr. Javier Ramón – IBEC
· Jorge Fuentes,
Business Strategy, A_Ventures, Barcelona, Spain
Follow us on Twitter: @Biorephealth