Cell Selection System for Migratory Subpopulation Isolation
Find Innovative SolutionsGenerate Solutions
Solution Overview
Problem
Current cell-based therapies for degenerative diseases face challenges such as unpredictable phenotype maintenance, survival, and migration of transplanted stem cells in the central nervous system, leading to suboptimal therapeutic outcomes.
Innovation Solution
A method for in vitro selection of therapeutic cell subpopulations from mesenchymal stem cells and astroglia using a cell culture system with a selection agent having openings of 8-12 μm diameter, allowing cells with increased migration potential to migrate into a separate reservoir, thereby isolating cells that can target specific tissues more effectively.
Engineering Contradictions & Design Principles
Engineering Contradiction Analysis
1Reliability
If stem cells are transplanted into the central nervous system, then therapeutic effects are achieved, but the cells fail to maintain desired phenotype, survive stably, or migrate to target areas
Solution Approach 1:
The patent applies preliminary action by pre-selecting and pre-differentiating stem cells in vitro before transplantation. The method involves culturing stem cells under specific conditions to induce differentiation into desired cell types (such as neurons or glial cells) and selecting cells with high migration potential before they are transplanted into the central nervous system. This preliminary preparation ensures that the transplanted cells have the correct phenotype and enhanced ability to migrate to target areas, thereby improving reliability while maintaining therapeutic efficacy.
2Ease of operation
If unselected stem cell populations are used, then cell therapy can be performed, but the cells lack sufficient migration potential to reach degenerated tissue
Solution Approach 1:
The patent applies the extraction principle by isolating and selecting specific subpopulations of stem cells that exhibit high migration potential from the total stem cell population. This is achieved through in vitro selection methods that identify and separate cells with enhanced migratory capabilities. By extracting this specific subpopulation, the patent ensures that the transplanted cells have sufficient migration speed to reach degenerated tissue effectively, while the overall cell therapy procedure remains feasible and manageable.
3Productivity
If stem cells are transplanted, then tissue regeneration is attempted, but the cells may migrate out of the transplanted area, preventing regeneration
Solution Approach 1:
The patent applies local quality by differentiating stem cells into specific cell types (such as neurons, astrocytes, or oligodendrocytes) that are appropriate for the specific type of tissue to be regenerated in the central nervous system. The differentiation process creates cells with localized functional properties and adhesion characteristics suited for their intended target tissue. This ensures that the transplanted cells not only remain in the transplanted area but also perform their specific regenerative functions effectively, thereby improving both retention and regeneration capability.
Applied Scientific Principles
This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.
Function Achieved in This Case
This method enables the targeted selection of cells with enhanced migration potential, leading to faster and more effective regeneration of degenerated tissue, improving the efficacy and safety of cell-based therapies.
Implementation Method 1
Application of an original cell population to an initial reservoir which is connected to at least one selection reservoir via at least one selection agent having at least one opening, the at least one opening of the at least one selection agent having a diameter of between 8 μm and 12 μm
Data Source
Figure 1A~1B
Figure 1C~1D
Figure 2
AI summary
The present invention relates to a method for the in vitro selection of at least one eukaryotic cell subpopulation from an original cell population. In said method, a reservoir system (10) comprising a starting reservoir (20) and at least one selection reservoir (12, 13, 14, 15, 16, 17; 30) is used, and at least one selection means (18; 19) having at least one opening (19; 29) is used, through which opening the cell subpopulations migrate into the selection reservoirs (12, 13, 14, 15, 16, 17; 30), which are equipped with cell culture medium and possibly additional additives. The invention further relates to the use of the cells obtained by means of the method and to the use of the reservoir system.