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Cell Counting and Image Cytometry

Wound Healing

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Topic
Wound Healing
Chemotaxis
Invasion into Matrigel
Transwell Migration
Wound Healing

Perform a wound healing migration assay by monitoring and quantifying cell growth in a defined area

  1. Measure the confluence and cell count of cells migrated into the exclusion (scratch) zone
  2. Acquire multiple images of the same plate to produce a kinetic reading of wound healing
  3. Perform wound healing assay using brightfield and/or fluorescent imaging

Imaging and quantification of a wound healing assay

Wound healing migration assay

In a wound healing migration assay, a wound is produced on a fully confluent cell layer by a mechanical tool or by a device inhibiting cell growth in a defined area. The Celigo™ is used to image the entire well with a wound at multiple time points. Confluence is y calculated for each well. The increase of confluence directly measures cell migration.

The Celigo image cytometer wound healing application using the 96-well Platypus Oris™ plates

Removing the well stopper leaves an exclusion zone into where the cells migrate.

The Celigo image cytometer detects cell migrating into the exclusion zone either in brightfield or fluorescence.

Wound healing application protocol

  1. Seeded cells overnight
  2. Removed the well stopper from the Platypus Oris™ plate (alternatively, perform a manual scratch)
  3. Wells were imaged using The Celigo green channel (various exposure time for dim or bright GFP cells)

    a. Plate was acquired at: 0h, 19h, 24h, 43h and 71h post stopper removal

  4. Analysis

    a. Wound Healing application was setup with a 36% well mask reduction to define the analysis area

    b. Acquisition and analysis parameters were saved to re-use for all time points

Wound healing plate map

Plate map: Cell type and conditions

Legend: NC – Negative control, KD – Knockdown

Measuring the migration of GFP-labeled cells using Platypus Oris™ 96-well plates

Whole-well images are acquired and the analysis area is defined by the Celigo software.  The Celigo Wound Healing application reports the wound healing confluence and cell count for each well over time within the defined analysis area.

Migration whole well image

Whole well fluorescent image

Plate cells: Remove stopper and Image whole well in fluorescence.

Migration definition of analysis area

Definition of analysis area

Analysis area is defined by reducing well mask size (36% of the total well area).

Migration analysis area

Analysis area (Zoomed)

The Celigo measures and reports the confluence and cell count within the analysis area.

Wound healing quantification of GFP-labeled H1299 cells

Wound healing qualification of labeled h1299 cells BF

The Celigo generated growth curves at the well and plate level for H1299-GFP cells

  • Increased Wound Healing % = Wound Healing % (71h) – Wound Healing % (0h)
  • Two seeding densities were tested: 70% and 85%. These seeding densities refer to the confluence of the original plate that was used for seeding onto the Platypus Oris™ plate.
  • Data indicates that similar wound healing trends were seen for both 70 and 85 percent confluent samples.
  • In the table below, A549 cells appear to have migrated the least into the wound compared to other cell types in the study.
Mean increased wound healing percentage data 1
Mean increased wound healing percentage plot 1

The Celigo live cell analysis of wound healing imaging and quantification using brightfield analysis

Migration whole well image BF

Whole-well brightfield image

Plate cells: Remove stopper and image whole well in brightfield.

Migration definition of analysis area BF

Definition of analysis area 

Analysis area is defined by reducing well mask size (36% of the total well area).

Migration analysis area BF

Analysis area (Zoomed)

The Celigo measures and reports the confluence and cell count within the analysis area.

Cell type and plating density

The Celigo Wound Healing application reports the wound healing confluence and cell count for each well over time using bright field imaging without requiring dye staining or GFP transfection.
U87 and HepG2 cells were plates at initial confluence measurement of 70 and 85%.

Cell type and plating density data

Measuring the migration of labeled hepG2 cells using Platypus Oris™ 96-well plates

Migration of labeled hepg2 cells using platypus 0h

0 hours after stopper removal

Migration of labeled hepg2 cells using platypus 24h

24 hours after stopper removal

Migration of labeled hepg2 cells using platypus 43h

43 hours after stopper removal

Migration of labeled hepg2 cell using platypus 71h

71 hours after stopper removal

The top row of images shows the whole-well brightfield image with fill. The bottom row shows a zoomed view of the segmentation.

Wound healing quantification of labeled H1299 cells using brightfield analysis

Wound healing qualification of labeled h1299 cells BF
Increased wound healing percentage data plot
Mean increased wound healing percentage data

Live cell analysis of increased Wound Healing % = Wound Healing % (71h) – Wound Healing % (0h)
Two seeding densities were tested 70% and 85%. These seeding densities refer to the confluence of the original plate that was used for seeding onto the Platypus Oris™ plate.
Data indicates that similar wound healing trends between U87 and HepG2 cells were seen for both 70 and 85 percent confluent samples.

Comparison of wound healing confluence between brightfield and fluorescence analysis

Bright field confluence wound healing

Brightfield Analysis

Fluorescent confluence wound healing

Fluorescent Analysis

Bright field fluorescent comparison data wound healing
Bright field h1299 gfp 85 percent

Brightfield H1299-GFP (85%)

Fluorescent h1299 gfp 85 percent

Fluorescent H1299-GFP (85%)

Wound healing confluence between Brightfield and Fluorescence analysis showed no significant difference between the two analysis methods.

Wound Healing Assay using Schwann and HUVEC Cells in 24-Well Plate

Protocol

  1. Place Cyto-select insert into well
  2. Plate high number of cells so that confluence is reached overnight
  3. Remove insert (Ideal time 0)
  4. Read plate
  5. Add growth or conditioned media to wells
  6. Read plate at 0,4,8, 24, 31 hours

Zoom View of Schwann Cell Wound “Closure” Over the Course of 31 Hours

The diagram shows the area of the well shown in zoomed images 0, 4, 8, 24 and 31 hours.

Schwann cell wound closer at 0hrs

0 Hours

Schwann cell wound closure at 4hrs

4 Hours

Schwann cell wound closure at 8hrs

8 Hours

Schwann cell wound closure at 24hrs

24 Hours

Schwann cell wound closure at 31hrs

31 Hours

The Celigo wound healing application reports the wound healing confluence and cell count for each well.

For research use only. Not for use in diagnostic procedures.

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