Norbornene Polymer Cell Differentiation Promoter

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Solution Overview

Problem

Current methods for promoting the differentiation of cultured cells, such as those used in skin regenerative medicine, are time-consuming and costly, and existing promoters like fermented milk products and cherry extracts are not suitable for regenerative medicine applications due to their composition or limited effectiveness in advancing cells to the horny cell stage.

Innovation Solution

A norbornene-based polymer formed article is used as a cultured cell differentiation promoter, contacting cultured cells within a culture vessel to enhance differentiation, specifically increasing mRNA levels indicative of differentiation markers like loricrin, thereby accelerating the differentiation process.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If conventional differentiation-inducing methods are used, then cell differentiation occurs, but the process is time-consuming and costly

Engineering Contradiction:
Improvedifferentiation speedVSAvoidtime required for differentiation
Core Design Contradiction:
ProductivityVSLoss of time

Solution Approach 1:

The invention changes the physical-chemical parameters of the culture vessel surface by using specific polymer materials with controlled hydrophobicity and surface energy. This modifies the cell-substrate interaction parameters, thereby accelerating the differentiation process without requiring extended culture periods or additional chemical inducers

Inventive Principle:
Principle #35Parameter changes

Solution Approach 2:

The polymer-formed article acts as an intermediary between the culture medium and the cultured cells. It mediates cell-substrate adhesion and signaling, providing mechanical cues that promote differentiation. The material serves as a bridge that translates physical substrate properties into biological responses, enabling faster differentiation

Inventive Principle:
Principle #24Intermediary (Mediator)

2Productivity

If fermented milk product is used to promote differentiation, then hornification is promoted, but lactic acid bacteria contaminate the culture medium

Engineering Contradiction:
Improvedifferentiation promotionVSAvoidbacterial contamination
Core Design Contradiction:
ProductivityVSObject-affected harmful factors

Solution Approach 1:

The invention extracts and isolates the beneficial differentiation-promoting components from fermented milk products while eliminating the harmful lactic acid bacteria. The polymer material embodies the functional properties needed for differentiation promotion without the contamination risk, effectively separating the useful effect from the harmful agent

Inventive Principle:
Principle #2Taking out (Extraction)

3Quantity of substance

If cherry extract is used to promote differentiation, then mRNA production for keratin 10 and profilaggrin is promoted, but differentiation into horny cells is not achieved

Engineering Contradiction:
ImprovemRNA productionVSAvoiddifferentiation completion
Core Design Contradiction:
Quantity of substanceVSReliability

Solution Approach 1:

The invention changes the physical parameters of the culture substrate to provide mechanical cues that complement the chemical signals. By adjusting surface hydrophobicity, roughness, and elasticity of the polymer-formed article, the system creates optimal conditions for complete differentiation into horny cells, not just intermediate mRNA expression

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentEP3162891B1Cultured cell differentiation promotion method and cultured cell differentiation promoter
Publication Date: 2019.12.11 ZEON CORP
  • EP3162891B1 patent drawingFigure 1
  • EP3162891B1 patent drawingFigure 2

AI summary

The present invention is a method that can promote the differentiation of cultured cells, and a cultured cell differentiation promoter that may suitably be used for the method. The differentiation of cultured cells is induced by bringing an alicyclic structure-containing polymer formed article into contact with cells that are being cultured.