Перегляд вихідного коду сторінки Completely New Viewpoint Around diglyceride Just Revealed

Tie1Cre transgenic mice are well characterized and have been shown to have extensive Cre activity in the majority of endothelial cells 28. By crossing ��6-floxed mice with Tie1Cre mice, we generated ��6-floxed/floxed-Tie1Cre+ (��6fl/fl-Tie1Cre+) mice. ��6fl/fl-Tie1Cre+ mice were born in normal Mendelian ratios. PCR of endothelial cells from ��6fl/fl-Tie1Cre+ [http://en.wikipedia.org/wiki/Diglyceride diglyceride] mice generated bands at 700 bp for the presence of the Cre insert, 154 bp for the ��6-floxed allele, and 120 bp for the wild-type allele (Figure 2a). Together with flow cytometric, immunofluorescence, and western blot analyses, these data confirmed that ��6-integrin expression was deleted successfully in the endothelial cells isolated from the ��6fl/fl-Tie1Cre+ mice (Figures 2b�C2d). Age-matched ��6fl/fl-Tie1Cre? and ��6fl/fl-Tie1-Cre+ mice were injected subcutaneously with either 1 �� 106 B16F0 murine melanoma cells or 0.5 �� 106 Lewis lung carcinoma (LLC) cells, and tumour size was measured at 10 or 12 days, respectively. Both B16F0 and LLC tumour sizes were significantly larger in ��6fl/fl-Tie1Cre+ mice than in ��6fl/fl-Tie1Cre? controls (**p [http://www.selleckchem.com/products/AZD8055.html AZD8055 nmr] that there was a significant increase in tumour blood vessel density in ��6fl/fl-Tie1Cre+ mice compared with ��6fl/fl-Tie1Cre? controls (*p [http://www.selleckchem.com/products/S31-201.html www.selleckchem.com/products/S31-201.html] unchallenged skin of ��6fl/fl-Tie1Cre? and ��6fl/fl-Tie1Cre+ mice showed no difference in vascularization (Supporting information, Supplementary Figure 1). To confirm the loss of ��6 in tumour blood vessels in vivo, cryosections of B16F0 tumours from ��6fl/fl-Tie1Cre? and ��6fl/fl-Tie1Cre+ mice were double-immunostained for ��6-integrin and a blood vessel marker. Since all the other blood vessel marker antibodies were the same species as the ��6 antibody, we used ��SMA to detect blood vessels. The staining revealed that ��6-integrin was significantly reduced in the ��6fl/fl-Tie1Cre+ tumour blood vessels (*p