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. Author manuscript; available in PMC: 2019 Jun 7.
Published in final edited form as: Cell Rep. 2019 May 7;27(6):1755–1768.e4. doi: 10.1016/j.celrep.2019.04.049

Figure 3. Endothelial-Specific Tlr4 Deletion with a Tie2-Cre Driver Protects against LPS-Induced Preterm Birth.

Figure 3.

(A) DIG-in situ hybridization for Tlr4 in decidual endothelia of Tlr4f/f and PgrCre/+Tlr4f/f mice on day 16 of pregnancy. Blue color indicates the Tlr4 signal. Dec, decidua. Arrow heads indicate blood vessels (Bv). Scale bar, 100 μm.

(B) PR (progesterone receptor)-positive cells are absent in the endothelium in days 4 (left) and 16 (right) uteri. Arrow head indicates blood vessel. Scale bars for the left and right panels represent 50 μm and 200 μm, respectively.

(C and D) The ratio of preterm birth (C) and dead pups (D) compared to total number of pups in Tlr4f/f and Tie2Cre/+Tlr4f/f mice with or without a high dose of LPS (40 μg/mouse). n, number of dams examined.

(E) Parturition timing in Tlr4f/f and Tie2Cre/+Tlr4f/f mice with or without LPS. n, number of dams examined.

(F) Dark-field and bright-field images of in situ hybridization for Cox2 in Tlr4f/f and Tie2Cre/+Tlr4f/f deciduae after 1 h of LPS exposure (40 μg/mouse). Arrow heads indicate blood vessels. Scale bar, 500 μm.

(G) Dark-field and bright-field images of in situ hybridization for Il6 in Tlr4f/f and Tie2Cre/+Tlr4f/f deciduae after 1 h of LPS exposure (40 μg/mouse). Arrow heads indicate blood vessels. Scale bar, 500 μm.

See also Figure S4.