Methods for Accelerated and Enhanced Cardiac Differentiation of IPS Cells by Electrical Stimulation
US-2016201035-A1 · Jul 14, 2016 · US
US11746328B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-11746328-B2 |
| Application number | US-201816490302-A |
| Country | US |
| Kind code | B2 |
| Filing date | Mar 3, 2018 |
| Priority date | Mar 3, 2017 |
| Publication date | Sep 5, 2023 |
| Grant date | Sep 5, 2023 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
Methods of inducing functional maturation of immature cardiomyocytes derived from induced pluripotent stem cells (iPSCs) and embryonic stem cells (ESCs) by electrically pacing the immature cardiomyocytes according to a pulse profile that induces maturation until the immature cardiomyocytes mature into functionally adult cardiomyocytes.
Opening claim text (preview).
What is claimed is: 1. A method of maturing functionally immature cardiomyocytes, the method comprising: a) providing a system configured to culture, electrically pace, and monitor beating of beating cells; b) culturing immature cardiomyocytes in the system; c) determining whether or not beating of the immature cardiomyocytes is synchronized by electrically monitoring the immature cardiomyocytes; d) if the beating is not synchronized, electrically pacing the immature cardiomyocytes until the cardiomyocyte beating is synchronized; and e) if the beating is synchronized, electrically pacing the immature cardiomyocytes according to a pulse profile that induces maturation until the immature cardiomyocytes mature into functionally adult cardiomyocytes; wherein the electric pacing in step 1d) is at a different pulse frequency than the electric pacing of step 1e). 2. The method of claim 1 , wherein the electric monitoring of the immature cardiomyocytes is by a method selected from the group consisting of monitoring cell-substrate impedance of the immature cardiomyocytes, performing extracellular recording of the immature cardiomyocytes, and both monitoring cell-substrate impedance and performing extracellular recording of the immature cardiomyocytes. 3. The method of claim 1 , wherein the pulse profile comprises one or more characteristics selected from the group consisting of a rectangular pulse shape, a pulse intensity of 0.7 V to 1 V, a pulse duration from 0.1 milliseconds to 0.2 milliseconds, and a pulse frequency between 1 Hz and 2 Hz. 4. The method of claim 1 , wherein the pulse profile comprises an increasing pulse frequency over time, optionally from 0.75 Hz to 2 Hz. 5. The method of claim 1 , wherein the immature cardiomyocytes are paced until displaying a positive beating force-frequency relationship in step e).
Culture process characterised by the use of electromagnetic stimulation · CPC title
from artificially induced pluripotent stem cells · CPC title
Circuits therefor (measuring impedance per se G01R27/02) · CPC title
Artificially induced pluripotent stem cells, e.g. iPS · CPC title
Cardiomyocytes; Heart cells · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.