Extended Data Fig. 2: Derivation of Mural-Tlr4KO mice and systemic phenotype following high fat diet feeding.
From: Perivascular mesenchymal cells control adipose-tissue macrophage accrual in obesity

a, Mural-Tlr4KO (PdgfrbrtTA; TRE-Cre; Tlr4loxP/loxP) mice were generated by breeding the PdgfrbrtTA transgenic mice to animals expressing Cre recombinase under the control of the tetracycline-response element (TRE-Cre) and carrying floxed Tlr4 alleles (Tlr4loxP/loxP). Littermates carrying only PdgfrbrtTA and Tlr4loxP/loxP alleles (that is Cre-) were used as the control animals (Control). The addition of doxycycline (Dox) leads to inactivation of Tlr4 in Pdgfrb-expressing cells. b, Intraperitoneal glucose tolerance tests (GTT) of RT-housed Control (n=9) and Mural-Tlr4KO (n=6) mice after HFD feeding. * denotes p< 0.05 by unpaired two-tailed Student’s t-test. c, Intraperitoneal insulin tolerance tests (ITT) of RT-housed Control (n=9) and Mural-Tlr4KO (n=6) mice after HFD feeding. * denotes p< 0.05 by unpaired two-tailed Student’s t-test. d–f, Levels of total monocytes and pro-inflammatory monocytes (LY6C+) in blood (d), bone marrow (e), and spleen (f) of Control (n=8) and Mural-Tlr4KO (n=8) mice after 5 months of HFD feeding. Bars represent mean ± s.e.m. Exact p values can be found in Source Data Extended Data Figure 2. Data were reproduced two times in independent experiments.