Mammary ductal morphogenesis requires paracrine activation of stromal EGFR via ADAM17-dependent shedding of epithelial amphiregulin
Development Sternlicht et al.
132: 3923
Supplemental Figure 1
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Fig.
S1. Differential
expression and signal intensity plots for potential interacting genes in
5-week-old mouse mammary glands. Modified Log2-Log10
MA-plots in which arithmetic means and standard deviations were obtained after
the fluorescence intensity ratios for TEBs or ducts versus distal stroma (M=Log2(Cy5/Cy3))
and mean overall signal intensities (A=0.5[log2(Cy5) + log2(Cy3)])
were converted to linear values for each of six independent arrays are shown
for the ERBB ligands on the TEB versus distal stroma (A) and duct versus distal
stroma arrays (B) and for the ADAMs and TIMPs represented on the TEB versus
distal stroma (C) and duct versus distal stroma arrays (D). The relative
expression ratio of 1 (equivalent expression) and mean overall expression value
of 2A=256 (A=8, below which it was difficult to distinguish true
signal from noise) are shown as broken lines. (A,B) AREG is expressed at high
levels and relatively concentrated in TEBs and ducts. NRG4 is expressed at
higher levels in the stroma than in TEBs or ducts. All other ERBB ligands are
neither readily detectable nor highly expressed at high levels in any tissue
compartment. (C,D) All ADAMs on the array are expressed; ADAM17 is equivalently
expressed in stromal and epithelial compartments; TIMP1 is expressed at high
levels in the TEB (but not duct) compartment; TIMP3 is more expressed ay higher
levels in the stroma than in the TEBs. (E) The relative and absolute expression
of TIMP1 is greater in TEBs and distal stroma than in ducts and distal stroma;
the relative and absolute values for TIMP3 are lower in TEBs and distal stroma
than in the ducts and distal stroma; ADAM17 is similarly expressed in ducts,
TEBs and distal stroma.