scholarly journals Induction of Anisotropic Orientation and Enhancement of Gene Functional Expression of Human Pluripotent Stem Cell-Derived Cardiomyocytes Cultured on Nanofabricated Substrates Consisting of Micron Planar Lines and Nano Dot Structures.

Author(s):  
Hisako Tokuno ◽  
Kotaro Dai ◽  
Kei Shinotsuka

Abstract Human-induced pluripotent stem cell-derived cardiomyocytes (hiPS-CMs) are expected to have applications in the fields of regenerative medicine and drug discovery. However, the immaturity of hiPS-CMs is an issue to be considered, and in order to replicate in vivo responsivity, there have been several attempts to induce maturation in hiPS-CMs, including methods to induce differentiation of hiPS-CMs by changing culture medium and culture substrate. In particular, anisotropic culture, in which the cultured cells are aligned in one direction, induces the cellular morphology resembling that of in vivo cardiomyocytes and is expected to be a useful method for maturation of hiPS-CMs. We tried forming a nanostructure on the surface of the cell culture substrate using our original nanofabrication technology, with the aim of aligning cardiomyocytes and inducing maturation. Our newly developed nanostructure for anisotropic culture (line/dot structure) comprises a region of cone-shaped nanopillars with pitch distance of several hundred nm and a planar region, alternating in a striped pattern with intervals of several tens of µm, arranged on the surface of the cell culture substrate. The hiPS-CMs cultured using the line/dot structure showed anisotropic orientation, and increased mRNA expression was observed in myocardial structural protein genes, genes relating to ion channels, and the gene for Cx43. These results suggest that the line/dot nanostructure is effective for anisotropic culture and cell maturation of hiPS-CMs.

2021 ◽  
Vol 4 (4) ◽  
pp. 3035-3040
Author(s):  
Sara Borrego-González ◽  
Berta de la Cerda ◽  
Francisco J. Díaz-Corrales ◽  
Aránzazu Díaz-Cuenca

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Gabriel Peinkofer ◽  
Martina Maass ◽  
Kurt Pfannkuche ◽  
Agapios Sachinidis ◽  
Stephan Baldus ◽  
...  

Abstract Background Induced pluripotent stem cell-derived cardiomyocytes (iPSC-CM) are regarded as promising cell type for cardiac cell replacement therapy, but it is not known whether the developmental stage influences their persistence and functional integration in the host tissue, which are crucial for a long-term therapeutic benefit. To investigate this, we first tested the cell adhesion capability of murine iPSC-CM in vitro at three different time points during the differentiation process and then examined cell persistence and quality of electrical integration in the infarcted myocardium in vivo. Methods To test cell adhesion capabilities in vitro, iPSC-CM were seeded on fibronectin-coated cell culture dishes and decellularized ventricular extracellular matrix (ECM) scaffolds. After fixed periods of time, stably attached cells were quantified. For in vivo experiments, murine iPSC-CM expressing enhanced green fluorescent protein was injected into infarcted hearts of adult mice. After 6–7 days, viable ventricular tissue slices were prepared to enable action potential (AP) recordings in transplanted iPSC-CM and surrounding host cardiomyocytes. Afterwards, slices were lysed, and genomic DNA was prepared, which was then used for quantitative real-time PCR to evaluate grafted iPSC-CM count. Results The in vitro results indicated differences in cell adhesion capabilities between day 14, day 16, and day 18 iPSC-CM with day 14 iPSC-CM showing the largest number of attached cells on ECM scaffolds. After intramyocardial injection, day 14 iPSC-CM showed a significant higher cell count compared to day 16 iPSC-CM. AP measurements revealed no significant difference in the quality of electrical integration and only minor differences in AP properties between d14 and d16 iPSC-CM. Conclusion The results of the present study demonstrate that the developmental stage at the time of transplantation is crucial for the persistence of transplanted iPSC-CM. iPSC-CM at day 14 of differentiation showed the highest persistence after transplantation in vivo, which may be explained by a higher capability to adhere to the extracellular matrix.


2021 ◽  
Author(s):  
Jitske Jansen ◽  
Bartholomeus T van den Berge ◽  
Martijn van den Broek ◽  
Rutger J Maas ◽  
Brigith Willemsen ◽  
...  

Nephrotic syndrome (NS) is characterized by severe proteinuria as a consequence of kidney glomerular injury due to podocyte damage. In vitro models mimicking in vivo podocyte characteristics are a prerequisite to resolve NS pathogenesis. Here, we report human induced pluripotent stem cell derived kidney organoids containing a podocyte population that heads towards adult podocytes and were superior compared to 2D counterparts, based on scRNA sequencing, super-resolution imaging and electron microscopy. In this study, these next-generation podocytes in kidney organoids enabled personalized idiopathic nephrotic syndrome modeling as shown by activated slit diaphragm signaling and podocyte injury following protamine sulfate treatment and exposure to NS plasma containing pathogenic permeability factors. Organoids cultured from cells of a patient with heterozygous NPHS2 mutations showed poor NPHS2 expression and aberrant NPHS1 localization, which was reversible after genetic correction. Repaired organoids displayed increased VEGFA pathway activity and transcription factor activity known to be essential for podocyte physiology, as shown by RNA sequencing. This study shows that organoids are the preferred model of choice to study idiopathic and congenital podocytopathies.


2019 ◽  
Vol 128 (2) ◽  
pp. 209-217 ◽  
Author(s):  
Kei Yoshida ◽  
Mika Okada ◽  
Risako Nagasaka ◽  
Hiroto Sasaki ◽  
Mai Okada ◽  
...  

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