开展6 000和10 000 k N·m能级强夯的现场试验,以强夯前后多道瞬态面波测试和重型动力触探试验方法,对强夯处理效果进行测试。试验结果表明:强夯加固处理后地基承载力和土体工程特性得到改善,但地基承载力特征值和压缩模量局部深度...开展6 000和10 000 k N·m能级强夯的现场试验,以强夯前后多道瞬态面波测试和重型动力触探试验方法,对强夯处理效果进行测试。试验结果表明:强夯加固处理后地基承载力和土体工程特性得到改善,但地基承载力特征值和压缩模量局部深度仍不能满足设计要求;6 000和10 000 k N·m能级有效加固深度分别为6.0~7.0 m和7.0~8.0 m;10 000 k N·m能级试验区浅层加固处理效果较差,与浅层存在淤泥质土、夯坑回填方式及第3遍夯点间距过大和夯能过小等因素有关,需采取相应的处理措施。展开更多
Deletion of HAX1 in mice causes a severe reduction in the numbers of lymphocytes in the bone marrow and in the spleen. Additionally, B220＋ B progenitor cells in the bone marrow are reduced, suggesting an important fu...Deletion of HAX1 in mice causes a severe reduction in the numbers of lymphocytes in the bone marrow and in the spleen. Additionally, B220＋ B progenitor cells in the bone marrow are reduced, suggesting an important function of HAX1 in B cell development. HAX1 is thought to play a protective role in apoptotic processes; therefore, we investigated the role of HAX1 in bone marrow B progenitor cells and splenic B cells. We did not observe an effect on the survival of Hax1-/- bone marrow cells but detected enhanced survival of splenic Hax1-/- B cells upon in vitro starvation/ growth-factor withdrawal. To explain this apparent inconsistency with previous reports of HAX1 function, we also studied the B cell receptor （BCR）-induced apoptosis of IgM-stimulated splenic naive B cells and found that apoptosis decreased in these cells. We further found impaired internalization of the BCR from Hax1-/- splenic B cells after IgM crosslinking; this impaired internalization may result in decreased BCR signaling and, consequently, decreased BCR-mediated apoptosis. We measured HAX1 binding to the cytoplasmic domains of different Ig subtypes and identified KVKWI（V）F as the putative binding motif for HAX1 within the cytoplasmic domains. Because this motif can be found in almost all Ig subtypes, it is likely that HAX1 plays a general role in BCR-mediated internalization events and BCR-mediated apoptosis.展开更多
文摘开展6 000和10 000 k N·m能级强夯的现场试验,以强夯前后多道瞬态面波测试和重型动力触探试验方法,对强夯处理效果进行测试。试验结果表明:强夯加固处理后地基承载力和土体工程特性得到改善,但地基承载力特征值和压缩模量局部深度仍不能满足设计要求;6 000和10 000 k N·m能级有效加固深度分别为6.0~7.0 m和7.0~8.0 m;10 000 k N·m能级试验区浅层加固处理效果较差,与浅层存在淤泥质土、夯坑回填方式及第3遍夯点间距过大和夯能过小等因素有关,需采取相应的处理措施。
文摘Deletion of HAX1 in mice causes a severe reduction in the numbers of lymphocytes in the bone marrow and in the spleen. Additionally, B220＋ B progenitor cells in the bone marrow are reduced, suggesting an important function of HAX1 in B cell development. HAX1 is thought to play a protective role in apoptotic processes; therefore, we investigated the role of HAX1 in bone marrow B progenitor cells and splenic B cells. We did not observe an effect on the survival of Hax1-/- bone marrow cells but detected enhanced survival of splenic Hax1-/- B cells upon in vitro starvation/ growth-factor withdrawal. To explain this apparent inconsistency with previous reports of HAX1 function, we also studied the B cell receptor （BCR）-induced apoptosis of IgM-stimulated splenic naive B cells and found that apoptosis decreased in these cells. We further found impaired internalization of the BCR from Hax1-/- splenic B cells after IgM crosslinking; this impaired internalization may result in decreased BCR signaling and, consequently, decreased BCR-mediated apoptosis. We measured HAX1 binding to the cytoplasmic domains of different Ig subtypes and identified KVKWI（V）F as the putative binding motif for HAX1 within the cytoplasmic domains. Because this motif can be found in almost all Ig subtypes, it is likely that HAX1 plays a general role in BCR-mediated internalization events and BCR-mediated apoptosis.
