Figure 6
Figure 6. Bleeding time and thromboembolism in ERα, ERβ, or ERα AF-10 hematopoietic chimeric mice. (A) Tail-bleeding times of control mice (WT) engrafted with normal bone marrow (ERα+/+ and ERβ+/+) and treated or not with E2. (B) Tail-bleeding times of ERα−/− and ERβ−/− bone marrow chimeras treated or not with E2. (C) Mice engrafted with normal bone marrow or (D) with bone marrow from ERα−/− or ERβ−/− mice were treated or not with E2 and thromboembolism assays were performed as in Figure 5. Fourteen of 15 mice engrafted with ERα−/− bone marrow died whereas all (7 of 7) mice engrafted with ERβ−/− survived. (E) Thromboembolism assays were performed in mice engrafted with ERα AF-10 bone marrow and treated or not with E2. All non-E2–treated mice (8 of 8) died, whereas all E2-treated mice (9 of 9) survived.

Bleeding time and thromboembolism in ERα, ERβ, or ERα AF-10 hematopoietic chimeric mice. (A) Tail-bleeding times of control mice (WT) engrafted with normal bone marrow (ERα+/+ and ERβ+/+) and treated or not with E2. (B) Tail-bleeding times of ERα−/− and ERβ−/− bone marrow chimeras treated or not with E2. (C) Mice engrafted with normal bone marrow or (D) with bone marrow from ERα−/− or ERβ−/− mice were treated or not with E2 and thromboembolism assays were performed as in Figure 5. Fourteen of 15 mice engrafted with ERα−/− bone marrow died whereas all (7 of 7) mice engrafted with ERβ−/− survived. (E) Thromboembolism assays were performed in mice engrafted with ERα AF-10 bone marrow and treated or not with E2. All non-E2–treated mice (8 of 8) died, whereas all E2-treated mice (9 of 9) survived.

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