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. 2011 Dec 21;287(8):5574–5587. doi: 10.1074/jbc.M111.286120

FIGURE 4.

FIGURE 4.

Recruitment of LAMP1 on SCP. A, Western blot showing levels of LAMP1 on indicated purified phagosomes (80 μg of protein per lane). Flagellin was used as a loading control. Right panel of the figure indicates quantification of the data by densitometry. Results are represented as mean ± S.D. of three observations, normalized to the loading control. The amount of LAMP1 present on respective 5-min phagosome is arbitrarily chosen as 1 unit. Data from three independent experiments were analyzed by t test, and the significance is indicated by p values between the respective 120 min phagosomes (*). B, confocal image showing the localization of respective Salmonella (green) near Golgi (labeled with GM130-red) or their colocalization with LAMP1 (red), after 120 min of internalization into macrophages. Salmonella was visualized by probing with Salmonella H antiserum followed by Alexa 488-labeled anti-rabbit secondary antibody. Image represents a single x/y plane of a Z-section, and arrows indicate colocalization. Inset shows the enlarged region. The graphs represent the percentage of SCP positive for LAMP1 or in vicinity of Golgi from at least 50 observations.