Skip to main content
. 2017 Jun 23;7:4165. doi: 10.1038/s41598-017-04220-8

Figure 2.

Figure 2

Embryos and their nuclear architecture visualized by OCM. (a) Stages in oogenesis and embryonic development subjected to OCM scanning. At some stages only intracellular structures were visualized (structural imaging in a single time-point), in other – both the structures and the dynamics of cellular processes such as pronuclei formation and movement or cell divisions were imaged (time-lapse imaging). (b–e) Pronuclei and nucleoli in a mouse zygote (b), 2-cell embryo (c) and blastocyst (d), and in a porcine 1-cell embryo obtained by parthenogenetic activation of an oocyte (e). BF – bright field images. OCM images of mouse zygotes and 2-cell embryos (DTIsp #3 protocol) were processed with the minimum intensity projection over 15 μm (Procedure #2). The mouse blastocyst was imaged using DTIsp #3 protocol without spatial averaging (Procedure #1). OCM images of a porcine embryo (DTIsp #2) are shown without spatial averaging (Procedure #1). Asterisks indicate the nucleoli, arrows - specular light reflexes visible in the nuclei that label the nucleoli. Cropped regions are encircled with a dashed line. Scale bars represent 20 μm. See also Supplementary Videos S1S3 and S14 for more images of these cells.