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IACUC / LARC STANDARD PROCEDURES
SHORT-TERM IN VIVO LYMPHOCYTE HOMING
IN MICE (Posted May 2007)
Description of procedure:
Donor mice will be euthanized and lymphoid organs will be
harvested to prepare leukocytes for injection into the recipients of the same
genetic background. These leukocytes may be labeled with a non-toxic fluorescent
dye for tracking purposes. Recipient mice will be kept warm to facilitate
vasodilation and restrained briefly in a mouse restrainer. At time 0, antibody
or other test compound in sterile saline or phosphate buffered saline may be
injected i.v. into the tail vein. After 1 hr, the mouse is again briefly restrained
in a mouse restrainer, and 3 x 10e6 leukocytes from the donor mice in sterile saline
or phosphate buffered saline are injected i.v. (tail vein). The mouse is returned to
the cage Endpoints for each experiment are varied, the timeline will be specified in
the individual protocol.
Mice will also be evaluated for general appearance, ability to
move normally around cage and reach food and water, ability to eat and drink, grooming
habits, skin color, lethargy, aggression (animals will be housed individually if
aggressive behavior is shown). Mice will be monitored for 15 min following each i.v.
injection and the following day (in the case of the 18 hr experiments).
The mouse will be euthanized immediately if the mouse displays
any evidence of respiratory distress or problems with normal movement. All mice will
be euthanized at termination of the experiment.
Literature search words required:
Literature search was performed for refinement of this Standard Procedure on April 9, 2007
| Key Words |
Search Site |
Years Covered |
| Lymphocyte homing in mice |
Pubmed |
1972- present |
Agents:
This procedure requires fluorescent dye, test compound,
saline. All agents administered to animals should be listed in the "Agents" section of RIO.
Adverse Effects:
| Procedure, Agent or Phenotype |
Potential Adverse Effects |
Management |
| Tail vein injections |
Reaction to agent, lethargy, labored breathing |
Euthanasia |
Monitoring Parameters:
| Monitoring Parameters |
Frequency |
PI/Lab will Document |
| General appearance/activity |
For 15 minutes after each IV injection and then the next day for 18 hr experiments |
No |
| Describe the conditions, complications, and criteria
(e.g. uncontrolled infection, loss of more than 15% body weight, etc.) that would
lead to removal of an animal from the study, and describe how this will be
accomplished (e.g. stopping treatment, euthanasia). |
| Labored breathing, euthanasia. |
| For all investigators housing animals with tumor formation,
skin lesions, neurological deficits, or that are in Category E, list the expected
characteristics/clinical presentations and endpoints of the animal model and the
criteria for euthanasia. Note: The IACUC also requires such lists to be posted in the
respective animal rooms and monitored by the IACUC compliance staff and LARC, to assure
PI adherence to the endpoints listed. |
| N/A. |
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