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 JoVE Biology

Isolation of Human Umbilical Vein Endothelial Cells (HUVEC)

1, 1, 1

1Department of Molecular Biology and Biochemistry, University of California, Irvine (UCI)

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    Summary

    This video protocol illustrates the isolation and culture of human umbilical vein endothelial cells (HUVEC) from human umbilical cord. Once isolated these cells can be used for in vitro angiogenesis assays like the Optimized Fibrin Gel Bead Assay also demonstrated by the Hughes lab.

    Date Published: 4/28/2007, Issue 3; doi: 10.3791/183

    Cite this Article

    Davis, J., Crampton, S. P., Hughes, C. C. Isolation of Human Umbilical Vein Endothelial Cells (HUVEC). J. Vis. Exp. (3), e183, doi:10.3791/183 (2007).

    Abstract

    Angiogenesis is a complex multi-step process, where in response to angiogenic stimuli, new vessels are created from the existing vasculature. These steps include: degradation of the basement membrane, proliferation and migration (sprouting) of endothelial cells (EC) into the extracellular matrix, alignment of EC into cords, lumen formation, anastomosis, and formation of a new basement membrane. Many in vitro assays have been developed to study this process, but most only mimic certain stages of angiogenesis, and morphologically the vessels often do not resemble vessels in vivo. Here we demonstrate an optimized in vitro angiogenesis assay that utilizes human umbilical vein EC and fibroblasts. This model recapitulates all of the key early stages of angiogenesis, and importantly the vessels display patent intercellular lumens surrounded by polarized EC. Vessels can be easily observed by phase-contrast and time-lapse microscopy, and recovered in pure form for downstream applications.

    Protocol

    Procedure

    1. Lay cord on clean pad and dab off excess blood. Make fresh cuts on both ends of the cord.
    2. Insert 21 1/2 G needle with the plastic needle sheath ON, into the vein. (The vein is the largest opening; the 2 smaller ones are arteries)
    3. Clamp the needle in place with a hemostat and attach the 20cc syringe of Hanks to the needle.
    4. Push the Hanks through the vein with moderate pressure. Collect the waste in the beaker with bleach. (Holding the needle and cord with one hand while pushing would prevent the needle popping out of the vein.) If there is a lot of blood in vein, wash a second time.
    5. Lay cord on pad and clamp the other end of the vein. Fill with a few mL of Hanks to check for leaks along the cord. Withdraw the 5 mL and disconnect the bottom clamp.
    6. Disconnect the 20cc syringe. Remove the plunger from the 10cc syringe. Attach 10cc syringe to needle, pour in 10ml collagenase and replace plunger. Push collagenase into vein until you see the first amount exit the open end. Re-clamp the open end and fill with collagenase until there is moderate distention of vein. Too much distention results in smooth muscle contamination.
    7. Massage the cord gently.
    8. Incubate cord (with hemostats, needle and syringe attached) in DPBS at 37°C for 15 min.
    9. While incubating, continue steps 1-8 with 2nd cord.
    10. After incubation, take cord out of beaker and while holding the cord over the 50mL tube cut the end above the bottom clamp. Be sure to collect everything in the tube. Push the remaining collagenase through the cord, then attach the 20cc syringe and push Hanks through with moderate pressure.
    11. If no smooth muscle cells are needed, discard the cord at this time. Otherwise, place the same cord into a second 50mL tube with ~5ml collagenase and incubate at 37°C for 30-60 min.
    12. Keep the tube until all cords are done.
    13. Spin tubes at ~1200 rpm for 5 min.
    14. Aspirate supernatant (except for ~1-2 mL). Resuspend the pellet in 5mls PHEC+ and plate in a T25.
    15. Incubate at 37°C with 5% CO2 overnight.
    16. Next day remove supernatant and replace with fresh media. If there are many RBCs, wash once with M199, then add PHEC+. Continue incubating as usual until the plate is confluent (1-4 days). Split into a gelatinized T75.
    17. Once T75 is confluent, split into three T75s. Freeze two vials per flask.

    Note: Endothelial cells (unactivated) have a cobblestone appearance. Endothelial cells are sometimes activated (long and pointy) right after isolation, after a couple of passes they usually return into an unactive state.

    Cleanup

    1. Very carefully, dispose of needles in sharps container.
    2. Dispose of syringes in big biohazard container.
    3. Put all tissue into small biohazard bag. Close bag and freeze at -20° until incineration.
    4. Soak all instruments in virucide for at least 10 min.
    5. Add incubation media to waste/bleach beaker. Let sit for at least 10 min.
    6. Discard the bench pads into biohazard waste.
    7. Spray down the inside and outside of beakers, bench top and the water bath lid with vircide. Let sit 10 min, then wipe.
    8. Rinse beakers and instruments with warm water and hang on rack to dry (blot off the instruments so they don't rust).
    9. Dispose of decontaminated waste down the sink.
    10. Return unused media to fridge.
    11. Dispose of gloves in biohazard waste.

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    Disclosures

    Materials

    Name Company Catalog Number Comments
    0.1% Collagenase 10ml per cord, warmed to 37°C
    Tissue culture flasks T75, one per cord.
    Hanks medium
    scissors sterile
    beaker sterile
    50 ml tubes

    Comments

    10 Comments

    may you tell me wath kind of collagenase do you use? thank you!
    Reply

    Posted by: AnonymousMay 16, 2008, 5:47 AM

    hi   i have been using dispase to isolate cells. iam succeeding in getting the cells but they are not spreading properly . even after two days iam not able to see  the typical cobble stone appearance. can you help.  Rathna  
    Reply

    Posted by: AnonymousJune 1, 2008, 11:25 AM

    hallo,can you tell me what's the  PHEC+ ?thank you !
    Reply

    Posted by: AnonymousDecember 15, 2008, 6:27 AM

    Hi, do you have any idea how many cells I can get from a 90% confluent flask (²5 or 75 qcm)? Many thanks in advance, Karin
    Reply

    Posted by: AnonymousAugust 26, 2009, 8:06 AM

    From my experience working with HUVEC, a confluent T²5 flask has about 400,000 to 600,000 million cells while a confluent T75 flask has approximately ²-4 millions cells. From this, you can probably roughly deduce how many cells are in a 90% confluent T²5/T75 flask. I hope this help.
    Reply

    Posted by: AnonymousSeptember 8, 2009, 5:45 AM

    hi
    how to i prepare collagenase for HUVEC isolation
    Reply

    Posted by: swati s.October 22, 2009, 1:45 PM

    Hi,

    I was a synthetic organic chemist and am trying to conduct a bio-organic project. I will be very thankful if you would share some info with me about how to lysate the HUVECs.

    Ge
    Reply

    Posted by: Ge Z.January 11, 2010, 6:56 PM

    To answer Ge's question, our lab lysate the HUVEC by adding lysate buffer 1x either in DPBS or water.
    Reply

    Posted by: AnonymousJanuary 20, 2010, 2:54 PM

    Thank you so much for the answer. May I have more info regarding the components of your lysate buffer and at what condition do you lysate HUVECs?
    Reply

    Posted by: AnonymousJanuary 20, 2010, 3:09 PM

    hi,

    Very Intresting way, but I wonder how many passages they can be usefull?
    Is there any difference between commercially available ones and freshly isolated ones(these ones)?
    Thanks in advance:-)
    Reply

    Posted by: AnonymousAugust 3, 2012, 11:57 AM

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