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. 2018 Nov 19;47(4):409–424.e9. doi: 10.1016/j.devcel.2018.10.026

Figure 1.

Figure 1

Centrosome Amplification Induces Paracrine Invasion

(A) Experimental flowchart.

(B) Left, quantification of invasive structures. Right, normal and invasive 3D acini. White arrowheads indicate invasive protrusions. Scale bar: 20 μM.

(C) Quantification of centrosome amplification.

(D) Quantification of invasive structures.

(E) Quantification of invasive structures.

(F) Top, schematic representation of mammary organoids isolation and growth. Bottom, non-invasive and invasive mammary organoids. Scale bar: 20 μM.

(G) Quantification of invasive organoids.

(H) Images of zebrafish injected with cells with (+DOX) or without (−DOX) extra centrosomes (left) or co-injected +DOX/−DOX (right).

(I) Incidence of invasive cells in zebrafish embryos. Number of injected fish −DOX = 121; +DOX = 103; and co-injection +/−DOX = 116.

(J) Number of disseminated cells in the zebrafish tail. Error bars represent mean ± SEM.

For all graphics, error bars represent mean ± SD from three independent experiments. p < 0.05, ∗∗p < 0.01, ∗∗∗p < 0.001, ∗∗∗∗p < 0.0001; ns not significant.

See also Figure S1; Videos S1, S2, S3, and S4; Table S1.