Current research in embryology by Sabine Globig

By Sabine Globig

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Marguerat S, Jensen TS, de Lichtenberg U, Wilhelm BT, Jensen LJ, Bahler J: The more the merrier: comparative analysis of microarray studies on cell cycleregulated genes in fission yeast. Yeast 2006, 23(4):261–277. 39. Jiang B, Kumar SD, Loh WT, Manikandan J, Ling EA, Tay SS, Dheen ST: Global gene expression analysis of cranial neural tubes in embryos of diabetic mice. J Neurosci Res 2008, 86(16):3481–3493. 40. Reece EA, Pinter E, Homko C, Wu Y-K, Naftolin F: The Yolk Sac Theory: Closing the Circle on Why Diabetes-Associated Malformations Occur.

5) using Trizol® (Invitrogen, Carlsbad, CA). We processed 2 controls and five diabetes-exposed embryos; the latter group included two specimen with neural tube defects (NTD) so as to capture the full phenotype spectrum of diabetes-exposure in pregnancy. Individual RNA samples (5 μg) from whole embryos were reverse transcribed (Invitrogen) and labeled (Affymetrix, Santa Clara, CA). 0 chips, which were scanned using a GeneChip3000 scanner; Affymetrix GCOS imaging software was used for quality control.

In response to implanting embryos the underlying endometrial stromal cells undergo decidualization that involves proliferation and differentiation through cell division and apoptosis [20,21]. Apoptosis is a physiological process which remodels tissue by removing expendable cells without allowing the entry of proteolytic enzymes and other harmful or corrosive substances into the surrounding tissue, and thus reducing the likelihood of an inflammatory response[22,23]. Localization of apoptotic cells in relation to the expression of apoptosis-related molecules, such as Fas/FasL, Bcl-2/Bax, and P53 have been demonstrated in the materno-fetal boundary of rhesus monkeys in pregnancy [24,25].

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