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. 2017 Oct 20;7:13708. doi: 10.1038/s41598-017-14053-0

Figure 2.

Figure 2

TEM images of vascularized iPSC-CM 3D-tissues 4 days after construction. (a) The iPSC-CMs (CM) are assembled to contact with each other within some amount of extracellular matrices (ECM) and the endothelial (blue) tubes (ET) extends along the iPSC-CMs. FB, fibroblast. (b) Higher magnification of the boxed area in a. Numerous myofilaments assemble to form myofibrils (mf), whereas some myofilaments with poor connectivity (white arrow) are also seen. Small mitochondria (m) with a few cristae are sparsely distributed within sarcoplasm. Black arrows, white and black arrowheads indicate sarcoplasmic reticula, Z-bands and desmosomes between the adjacent iPSC-CMs, respectively. (c) Higher magnification of the contact area of the iPSC-CMs. Many desmosomes (black arrowheads) are seen between the cells, but gap junction is indistinguishable. The cell at the top shows intracellular edema. White arrowheads indicate Z-bands of myofibrils (mf). m, mitochondria. (d) Higher magnification of the boxed area in a. The endothelial cells connect to each other by overlapping (arrows) with junctional complex (black arrowheads) to form vascular lumen. The endothelial pores (white arrowheads) are also seen. (e) A insertion of extracellular tissue (*) is seen in the endothelial cords (EC). CM, iPSC-CM. Inset: Higher magnification of the boxed area in e. The endothelial cell contains abundant rough endoplasmic reticula (rer), coated vesicles (black arrows), Golgi apparatuses (G) and lysosomes (white arrow). Scale bar: 500 nm.