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Devices and methods for isolating a migratory cell population

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  • Publication Date:
    April 01, 2025
  • معلومة اضافية
    • Patent Number:
      12264,305
    • Appl. No:
      16/574587
    • Application Filed:
      September 18, 2019
    • نبذة مختصرة :
      A method and device for isolating a migratory cell population from a mixed population of migratory cells and non-migratory cells is described herein. The method comprises placing the mixed population of migratory cells and non-migratory cells in contact with a device having one or more microchannels; and isolating the migratory cell population within the microchannels following an incubation period, wherein the one or more microchannels have an average size in a proliferation direction of the migratory cells that is less than a minimum proliferation space of the migratory cells along the proliferation direction.
    • Inventors:
      Board of Regents, The University of Texas System (Austin, TX, US); THE BOARD OF REGENTS OF THE UNIVERSITY OF OKLAHOMA (Norman, OK, US)
    • Assignees:
      BOARD OF REGENTS, THE UNIVERSITY OF TEXAS SYSTEM (Austin, TX, US), THE BOARD OF REGENTS OF THE UNIVERSITY OF OKLAHOMA (Norman, OK, US)
    • Claim:
      1. A method of isolating a migratory cell population from a mixed population of migratory cells and non-migratory cells, the method comprising: placing the mixed population of migratory cells and non-migratory cells in contact with one or more microchannels; commencing an incubation period to allow the migratory cells to migrate into the microchannels; isolating the migratory cell population within the microchannels following the incubation period by attaching the migratory cells to the surface of the microchannels; and collecting the migratory cell population from the microchannels, wherein the one or more microchannels have an average size in a proliferation direction of the migratory cells that is less than a minimum proliferation space of the migratory cells along the proliferation direction, and wherein at least 500 migratory cells are isolatable within the microchannels at the same time by carrying out the steps as a single method of placing the mixed population of migratory cells and non-migratory cells in contact with one or more microchannels, commencing an incubation period to allow the migratory cells to migrate into the microchannels, isolating the migratory cell population within the microchannels following the incubation period by attaching the migratory cells to the surface of the microchannels, and collecting the migratory cell population from the microchannels only once.
    • Claim:
      2. The method of claim 1 , wherein collecting the migratory cell population from the microchannels comprises extracting the migratory cell population from inside the microchannels.
    • Claim:
      3. The method of claim 1 , wherein the proliferation direction is horizontal and the mixed population of cells are eukaryotic.
    • Claim:
      4. The method of claim 1 , wherein the proliferation direction is vertical and the mixed population of cells are microbial.
    • Claim:
      5. The method of claim 1 , wherein the microchannels free of a chemoattractant.
    • Claim:
      6. The method of claim 1 , wherein the mixed population is placed in contact with a plurality of microchannels, and the plurality of microchannels comprise an array.
    • Claim:
      7. The method of claim 1 , wherein the microchannels are positioned in a cell culture.
    • Claim:
      8. The method of claim 1 , wherein the one or more microchannels have a cell receiving space with an average width of less than 10 μm that prevents cell proliferation within the microchannels.
    • Claim:
      9. The method of claim 1 , wherein the microchannels comprise an opening on one end.
    • Claim:
      10. The method of claim 1 , wherein each of the microchannels comprise an opening permeable to a liquid media via capillary action along the length of the microchannels.
    • Claim:
      11. The method of claim 1 , wherein the microchannels have sidewalls that are impermeable to the migratory and non-migratory cells.
    • Claim:
      12. The method of claim 1 , wherein placing the mixed population of migratory cells and non-migratory cells in contact with one or more microchannels comprises seeding the mixed population proximate an opening on an end of each of the microchannels.
    • Claim:
      13. The method of claim 1 , wherein placing the mixed population of migratory cells and non-migratory cells in contact with one or more microchannels comprises placing the one or more microchannels adjacent to seeded cells of the mixed population.
    • Claim:
      14. The method of claim 7 , wherein isolating the migratory cells within the microchannels comprises removing the microchannels from the cell culture.
    • Claim:
      15. The method of claim 1 , wherein the average size in the proliferation direction of the migratory cells confines the migratory cells to a native size of the migratory cells.
    • Claim:
      16. The method of claim 15 , wherein the native size of the migratory cells is the size of a whole cell or cell soma of the migratory cells while the migratory cells are in a non-dividing and non-differentiating state.
    • Claim:
      17. The method of claim 1 , wherein the one or more microchannels have an average width of less than 10 μm.
    • Patent References Cited:








    • Other References:
      Chen et al. Single-cell Migration Chip for Chemotaxis-based Microfluidic Selection of Heterogeneous Cell Populations. Scientific Reports (2015). 5(09980), 13 pages. (Year: 2015). cited by examiner
      Liu et al. A Microfluidic Device for Blood Cell Sorting and Morphology Analysis. 17th International Conference on Miniaturized Systems for Chemistry and Life Sciences (2013), 1003-1005 (Year: 2013). cited by examiner
      Invitrogen technical manual B-084243 0110 (“Cell Culture Basics” (2010), 56 pages. (Year: 2010). cited by examiner
      Baghat et al. Pinched flow coupled shear-modulated inertial microfluidics for high-throughput rare blood cell separation. Lab on a Chip (2011), 11, 1870-1878. (Year: 2011). cited by examiner
      Dean L. Blood Groups and Red Cell Antigens [Internet]. Bethesda (MD): National Center for Biotechnology Information (US); 2005. Chapter 1, Blood and the cells it contains. Available from: https://www.ncbi.nlm.nih.gov/books/NBK2263/ (Year: 2005). cited by examiner
      Mcfaul et al. Cell separation based on size and deformability using microfluidic funnel ratchets. Lab on a Chip (2012), 12, 2369- 2376. (Year: 2012). cited by examiner
      Meyer et al. Multi-depth valved microfluidics for biofilm segmentation. J. Micromech. Microeng. 25 (2015) 095003. (Year: 2015). cited by examiner
      Friedl et al., “Nuclear mechanics during cell migration”, Curr Opin Cell Biol., 23(1), 2011, pp. 55-64. cited by applicant
      Ridley et al., “Cell Migration: Integrating Signals from Front to Back”, Science, vol. 302, Issue 5651, 2003, pp. 1704-1709. cited by applicant
    • Primary Examiner:
      Barron, Sean C.
    • Attorney, Agent or Firm:
      Maynard Nexsen PC
      Zimmer, John P.
    • الرقم المعرف:
      edspgr.12264305