DLL3 expression perturbs the balance between neuroendocrine and non-neuroendocrine cells in a mouse model of SCLC
(A) Schematic representation of the Cre-inducible Dll3 allele and the genetically engineered mouse model of SCLC.
(B) Representative hematoxylin and eosin (H&E) staining of sections from RPR2;R26Luc and RPR2;R26Dll3mutant lungs (top, scale bar 1 mm) and lung tumors (bottom, scale bar 100 μm) 6 months after tumor initiation (n ≥ 6 mice).
(C) Representative flow cytometry analysis of DLL3 cell surface expression in SCLC cells from RPR2;R26Luc and RPR2;R26Dll3mutant mice 5.5 months after tumor initiation.
(D) Quantification of (C) (n = 5 independent experiments).
(E) As in (C) with RPR2;R26Luc SCLC cells differentiated by NCAM and ICAM expression.
(F) Quantification of (E) (n = 6 independent experiments).
(G) Representative flow cytometry dot plots of control cancer cells from RPR2;R26Luc tumors with no stain, stained cells from RPR2;R26Luc tumors, and stained cells from RPR2;R26Dll3 tumors (from left to right).
(H–J) Quantification of NCAMhigh ICAMlow, NCAMlow ICAMhigh, and NCAMlow ICAMlow populations in (G).
Unpaired t-test, data represented as mean ± s.d. ∗p<0.05, ∗∗p<0.01, ∗∗∗p<0.001. See also Figure S3.