This video demonstrates the tracking of leukocyte recruitment using transgenic zebrafish larvae expressing photoconvertible green fluorescent protein. Pre-injecting red fluorescent dye-labeled bacteria into the otic vesicle and inducing photoconversion enables observation of leukocytes' migration, phagocytosis, and dispersal throughout the body, providing valuable insights into immune response dynamics.
Protocol
1. Preparing Microinjection Needles Prepare thin wall glass capillary injection needles (1.0 OD/0.75 ID) using a micropipette puller device with the following settings: air pressure 200, heat 502, pull 90, velocity 80, time 70, air time at the start of pull 5, air time at end of pull 5. Using fine tweezers, break off the tip of the pulled needle so that the tip opening has a diameter of approximately 10 µm. 2. Preparing Larval Injection …
Representative Results
Figure 1: Leukocyte recruitment to otic vesicle infection with S. iniae. (A) Neutrophil recruitment to S. iniae infection. (i) Successful injection of a phenol red-labeled inoculum into the otic vesicle. (ii-iv) Sudan Black staining of larvae for investigation of neutrophil recruitment at 2 h…
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The authors have nothing to disclose.
Materials
1.7 ml eppendorfs
MidSci
AVSS1700
14 ml falcon tube
BD Falcon
352059
96 well plate
Corning Incorporated
3596
Agar
BD Biosciences
214030
CellTracker Red
Molecular Probes, Invitrogen
C34552
CNA agar
Dot Scientific, Inc
7126A
Disposable transfer pipets
Fisher Scientific
13-711-7m
Dissecting Scope
Nikon
SMZ745
DMSO
Sigma Aldrich
D2650
Fine tweezers
Fine Science Tools
11251-20
Gel comb
VWR
27372-482
4.2 mm width, 1.5 mm thick
Glass bottom dishes
Custom made by drilling a 16–18 mm hole in the center of a 35-mm tissue culture dish bottom and placing a 22-mm round #1 coverslip in the hole and sealing with a thin layer of Norland Optical Adhesive 68 cured by UV light.