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Mahbub, S. B.

Publications and source records attributed to Mahbub, S. B..

3 recordsLinked to original sources

Automated identification of aneuploid cells within the inner cell mass of an embryo using a numerical extraction of morphological signatures

STUDY QUESTIONCan artificial intelligence distinguish between euploid and aneuploid cells within the inner cell mass of mouse embryos using brightfield images? SUMMARY ANSWERA deep morphological signature (DMS) generated by deep learning followed by swarm intelligence and discriminative analysis can identify the ploidy state of inner cell mass (ICM) in the mouse blastocyst-stage embryo. WHAT IS KNOWN ALREADYThe presence of aneuploidy - a deviation from the expected number of chromosomes - is predicted to cause early pregnancy loss or congenital disorders. To date, available techniques to detect embryo aneuploidy in IVF clinics involve an invasive biopsy of trophectoderm cells or a non-invasive analysis of cell-free DNA from spent media. These approaches, however, are not specific to the ICM and will consequently not always give an accurate indication of the presence of aneuploid cells with known ploidy therein. STUDY DESIGN, SIZE, DURATIONThe effect of aneuploidy on the morphology of ICMs from mouse embryos was studied using images taken using a standard brightfield microscope. Aneuploidy was induced using the spindle assembly checkpoint inhibitor, reversine (n = 13 euploid and n = 9 aneuploid). The morphology of primary human fibroblast cells with known ploidy was also assessed. PARTICIPANTS/MATERIALS, SETTING, METHODSTwo models were applied to investigate whether the morphological details captured by brightfield microscopy could be used to identify aneuploidy. First, primary human fibroblasts with known karyotypes (two euploid and trisomy: 21, 18, 13, 15, 22, XXX and XXY) were imaged. An advanced methodology of deep learning followed by swarm intelligence and discriminative analysis was used to train a deep morphological signature (DMS). Testing of the DMS demonstrated that there are common cellular features across different forms of aneuploidy detectable by this approach. Second, the same approach was applied to ICM images from control and reversine treated embryos. Karyotype of ICMs was confirmed by mechanical dissection and whole genome sequencing. MAIN RESULTS AND THE ROLE OF CHANCEThe DMS for discriminating euploid and aneuploid fibroblasts had an area under the receiver operator characteristic curve (AUC-ROC) of 0.89. The presence of aneuploidy also had a strong impact on ICM morphology (AUC-ROC = 0.98). Aneuploid fibroblasts treated with reversine and projected onto the DMS space mapped with untreated aneuploid fibroblasts, supported that the DMS is sensitive to aneuploidy in the ICMs, and not a non-specific effect of the reversine treatment. Consistent findings in different contexts suggests that the role of chance low. LARGE SCALE DATAN/A LIMITATIONS, REASON FOR CAUTIONConfirmation of this approach in humans is necessary for translation. WIDER IMPLICATIONS OF THE FINDINGSThe application of deep learning followed by swarm intelligence and discriminative analysis for the development of a DMS to detect euploidy and aneuploidy in the ICM has high potential for clinical implementation as the only equipment it requires is a brightfield microscope, which are already present in any embryology laboratory. This makes it a low cost, a non-invasive approach compared to other types of pre-implantation genetic testing for aneuploidy. This study gives proof of concept for a novel strategy with the potential to enhance the treatment efficacy and prognosis capability for infertility patients. STUDY FUNDING/COMPETING INTEREST(S)K.R.D. is supported by a Mid-Career Fellowship from the Hospital Research Foundation (C-MCF-58-2019). This study was funded by the Australian Research Council Centre of Excellence for Nanoscale Biophotonics (CE140100003), the National Health and Medical Research Council (APP2003786) and an ARC Discovery Project (DP210102960). The authors declare that there is no conflict of interest.

bioinformatics↗

Oocyte and cumulus cell cooperativity and metabolic plasticity under the direction of oocyte paracrine factors

Mammalian oocytes develop and mature in a mutually dependent relationship with surrounding cumulus cells. The oocyte actively regulates cumulus cell differentiation and function by secreting soluble paracrine oocyte-secreted factors (OSFs). We characterized the molecular mechanisms by which two model OSFs, cumulin and BMP15, regulate oocyte maturation and cumulus-oocyte cooperativity. Exposure to these OSFs during maturation altered the proteomic and multispectral autofluorescence profiles of both the oocyte and cumulus cells. In oocytes, cumulin significantly upregulated proteins involved in nuclear function. In cumulus cells, both OSFs elicited marked upregulation of a variety of metabolic processes (mostly anabolic), including lipid, nucleotide, and carbohydrate metabolism, while mitochondrial metabolic processes were downregulated. The mitochondrial changes were validated by functional assays confirming altered mitochondrial morphology, respiration, and content, whilst maintaining ATP homeostasis. Collectively, these data demonstrate that OSFs remodel cumulus cell metabolism during oocyte maturation in preparation for ensuing fertilization and embryonic development. HIGHLIGHTSO_LIDuring oocyte maturation, oocyte-secreted factors promote cell cooperativity between the oocyte and cumulus cells by altering the molecular composition of both cell types. C_LIO_LIOocyte-secreted factors downregulate protein catabolic processes, and upregulate DNA binding, translation, and ribosome assembly in oocytes. C_LIO_LIOocyte-secreted factors alter mitochondrial number, morphology, and function in cumulus cells. C_LIO_LIOocyte-secreted factors further enhance metabolic plasticity in cumulus cells by upregulating anabolic pathways for macromolecules and small molecule organics. C_LIO_LIThe oocyte, via oocyte-secreted factors, instructs cumulus cells to increase metabolic workload on its behalf, thereby subduing oocyte metabolism. C_LI

developmental biology↗

Non-invasive, label-free optical analysis to detect aneuploidy within the inner cell mass of the preimplantation embryo

Study questionCan label-free, non-invasive optical imaging by hyperspectral microscopy discern between euploid and aneuploid cells within the inner cell mass of the mouse preimplantation embryo? Summary answerHyperspectral microscopy shows a variance in metabolic activity which enables discrimination between euploid and aneuploid cells. What is known alreadyEuploid/aneuploid mosaicism affects up to 17.3% of human blastocyst embryos with trophectoderm biopsy or spent media currently utilised to diagnose aneuploidy and mosaicism in clinical in vitro fertilisation. Based on their design, these approaches will fail to diagnose the presence or proportion of aneuploid cells within the fetal lineage (inner cell mass (ICM)) of some blastocyst embryos. Study design, size, durationThe impact of aneuploidy on cellular metabolism of primary human fibroblast cells and mouse embryos was assessed by a fluorescence microscope adapted for imaging with multiple spectral channels (hyperspectral imaging). Primary human fibroblast cells with known ploidy were subjected to hyperspectral imaging to record native cell fluorescence (euploid n= 467; aneuploid n= 969). For mouse embryos, 50-70 individual euploid and aneuploid blastomeres (8-cell stage embryo) and chimeric blastocysts (40-50 per group: euploid; aneuploid; or 1:1 and 1:3 ratio of euploid:aneuploid) were utilised for hyperspectral imaging. Participants/materials, setting, methodsTwo models were employed: (i) Primary human fibroblasts with known karyotype and (ii) a mouse model of embryo aneuploidy where mouse embryos were treated with reversine, a reversible spindle assembly checkpoint inhibitor, during the 4-to 8-cell division. Individual blastomeres were dissociated from reversine treated (aneuploid) and control (euploid) 8-cell embryos and either imaged directly or used to generate chimeric blastocysts with differing ratios of euploid:aneuploid cells. Individual blastomeres and embryos were subjected to hyperspectral imaging. Changes in cellular metabolism were determined by quantification of metabolic cofactors (inferred from their autofluorescence signature): reduced nicotinamide adenine dinucleotide (NAD(P)H), flavins with the subsequent calculation of the optical redox ratio (ORR: Flavins/[NAD(P)H + Flavins]). Mathematical algorithms were applied to extract features from the autofluorescence signals of each cell/blastomere/inner cell mass to discriminate between euploid and aneuploid. Main results and the role of chanceAn increase in the relative abundance of NAD(P)H with a decrease in flavins led to a significant reduction in the ORR for aneuploid cells in both primary human fibroblasts and individual mouse blastomeres (P < 0.05). Mathematical algorithms were able to achieve good separation between (i) euploid and aneuploid primary human fibroblast cells, (ii) euploid and aneuploid mouse blastomeres cells and (iii) euploid and aneuploid chimeric blastocysts and (iv) 1:1 and 1:3 chimeric blastocysts. The accuracy of these separations was supported by receiver operating characteristic curves with areas under the curve of 0.85, 0.99, 0.87 and 0.88, respectively. We believe that the role of chance is low as multiple cellular models (human somatic cells and mouse embryos) demonstrated a consistent shift in cellular metabolism in response to aneuploidy as well as the robust capacity of mathematical features to separate euploid and aneuploid cells in a statistically significant manner. Limitations, reasons for cautionThere would be added value in determining the degree of embryo mosaicism by sequencing the inner cell mass (ICM) of individual blastocysts to correlate with metabolic profile and level of discrimination achieved using the mathematical features approach. Wider implications of the findingsHyperspectral imaging was able to discriminate between euploid and aneuploid human fibroblasts and mouse embryos. This may lead to the development of an accurate and non-invasive optical approach to assess mosaicism within the ICM of human embryos in the absence of fluorescent tags. Study funding/competing interest(s)K.R.D. is supported by a Mid-Career Fellowship from the Hospital Research Foundation (C-MCF-58-2019). This study was funded by the Australian Research Council Centre of Excellence for Nanoscale Biophotonics (CEI40100003). The authors declare that there is no conflict of interest.

cell biology↗