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¡¾ÔÎÄժ¼¡¿Nature Cell Biology 12, 598 - 604 (2010)
A distinctive role for focal adhesion proteins in three-dimensional cell motility
Stephanie I. Fraley£¬Yunfeng Feng, Ranjini Krishnamurthy, Dong-Hwee Kim, Alfredo Celedon, Gregory D. Longmore & Denis Wirtz
Focal adhesions are large multi-protein assemblies that form at the basal surface of cells on planar dishes, and that mediate cell signalling, force transduction and adhesion to the substratum. Although much is known about focal adhesion components in two-dimensional (2D) systems, their role in migrating cells in a more physiological three-dimensional (3D) matrix is largely unknown. Live-cell microscopy shows that for cells fully embedded in a 3D matrix, focal adhesion proteins, including vinculin, paxillin, talin, ¦Á-actinin, zyxin, VASP, FAK and p130Cas, do not form aggregates but are diffusely distributed throughout the cytoplasm. Despite the absence of detectable focal adhesions, focal adhesion proteins still modulate cell motility, but in a manner distinct from cells on planar substrates. Rather, focal adhesion proteins in matrix-embedded cells regulate cell speed and persistence by affecting protrusion activity and matrix deformation, two processes that have no direct role in controlling 2D cell speed. This study shows that membrane protrusions constitute a critical motility/matrix-traction module that drives cell motility in a 3D matrix.
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¡¡¡¡¡¾ÕªÒª¡¿ScienceDaily (June 26, 2010) À´×ÔÃÀ¹ú¿ÆÑ§¼Ò·¢Ã÷£¬ºì¾ÆËùº¬µÄ°×޼«´¼£¨resveratrol£©¿ÉÒÔ±ÜÃâÓꦵÄѪ¹ÜÉú³¤£¬ÓÐÖú±ÜÃâÊÓÁ¦Ë¥ÍË¡£»ªÊ¢¶Ù´óѧҽѧԺµÄר¼ÒÀ½ðÀµÂ °¢ÆÕÌØÔÚ¡¶ÃÀ¹ú²¡ÀíѧÔÓÖ¾¡·ÉÏÖ¸³ö£¬°×޼«´¼¿ÉÒÔÖ±½ÓµØÒÖÖÆÑÛ¾¦ÄÚÍâµÄÒ쳣Ѫ¹ÜÐÂÉú¡£°×޼«´¼ÊÇÒ»ÖÖ¿¹Î¢ÉúÎïÎïÖÊ£¬¿ÉÓɶàݪֲÎï×ÔÈ»±¬·¢£¬¿ÉÒÔ±ÜÃâϸ¾úºÍÕæ¾úµÄѬȾ¡£ËüÔÚÆÏÌÑÆ¤ÀﺬÁ¿ÓÈÆä¸ß£¬Òò´ËÔÚºì¾ÆÖеķÖÁ¿ÒàÊ®·Ö¸»ºñ£»Æä´Î¾ÍÊÇÔÚÀ¶Ý®¡¢»¨ÉúµÈÖ²Îï¡£ÔÚÕâÏîÑо¿Ç°£¬Ò½Ñ§½çÒÑ·¢Ã÷°×޼«´¼ÓÐÖúÑÓ»ºÐàÂõºÍÔ¤·À°©Ö¢¡£Ò쳣Ѫ¹ÜÐÂÉúÊdz¤³ö²»¿µ½¡»òÍ»±äµÄѪ¹ÜµÄÕ÷Ïó£¬Óë°©Ö¢¡¢ÐÄÔಡÒÔ¼°ÑÛ¼²£¨ÈçÍíÄê»Æ°ß²¡±ä£©Ïà¹Ø¡£°¢ÆÕÌØÏàÐÅÕâÒ»Ñо¿Ð§¹û½«»á´ó´óÓ°Ïìҽѧ½ç¶Ô°×޼«´¼µÄÊìϤ£¬´Ù³ÉеÄÑÛ¼²ÁÆ·¨¡£ÖÚËùÖÜÖª£¬½üÄê²»ÉÙÑо¿·¢Ã÷ÊÊÁ¿ÒûÓÃºì¾Æ¿ÉÒÔΪ¿µ½¡´øÀ´Ä³Ð©Òæ´¦£¬³ýÁËÔ¤·ÀÖз磬»¹¿ÉÒÔÔ¤·ÀÐÄѪ¹Ü¼²²¡¡£²»ÉÙÈËÒÔΪºì¾Æµ¼ÖÂÁËËùνµÄ¡°·¨¹úµõ¹î¡±£¨French paradox£©µÄÕ÷Ï󣺷¨¹úÈËËäÈ»³£³ÔÅ£ÓÍ¡¢Ö¥Ê¿µÈ¸ß֬ʳÎÐÄѪ¹Ü¼²²¡µÄ·¢²¡ÂÊÈ´Æ«µÍ¡£
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¡¾ÔÎÄժ¼¡¿A. Khan, D. S. Dace, A. G. Ryazanov, J. Kelly, R. S. Apte. Resveratrol Regulates Pathologic Angiogenesis by a Eukaryotic Elongation Factor-2 Kinase-Regulated Pathway. American Journal Of Pathology, 2010; DOI: 10.2353/ajpath.2010.090836
Abnormal angiogenesis is central to the pathophysiology of diverse disease processes including cancers, ischemic and atherosclerotic heart disease, and visually debilitating eye disease. Resveratrol is a naturally occurring phytoalexin that has been demonstrated to ameliorate and decelerate the aging process as well as blunt end organ damage from obesity. These effects of resveratrol are largely mediated by members of the sirtuin family of proteins. We demonstrate that resveratrol can inhibit pathological angiogenesis in vivo and in vitro by a sirtuin-independent pathway. Resveratrol inhibits the proliferation and migration of vascular endothelial cells by activating eukaryotic elongation factor-2 kinase. The active kinase in turn phosphorylates and inactivates elongation factor-2, a key mediator of ribosomal transfer and protein translation. Functional inhibition of the kinase by gene deletion in vivo or RNA as well as pharmacological inhibition in vitro is able to completely reverse the effects of resveratrol on blood vessel growth. These studies have identified a novel and critical pathway that promotes aberrant vascular proliferation and one that is amenable to modulation by pharmacological means. In addition, these results have uncovered a sirtuin-independent pathway by which resveratrol regulates angiogenesis.
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¡¾ÔÎÄժ¼¡¿Nature 466, 133-137 (1 July 2010) | doi:10.1038/nature09161
Alexander D. Boiko, Olga V. Razorenova, Matt van de Rijn£¬et al.
The question of whether tumorigenic cancer stem cells exist in human melanomas has arisen in the last few years1. Here we show that in melanomas, tumour stem cells (MTSCs, for melanoma tumour stem cells) can be isolated prospectively as a highly enriched CD271+ MTSC population using a process that maximizes viable cell transplantation. The tumours sampled in this study were taken from a broad spectrum of sites and stages. High-viability cells isolated by fluorescence-activated cell sorting and re-suspended in a matrigel vehicle were implanted into T-, B- and natural-killer-deficient Rag2−/−¦Ãc−/− mice. The CD271+ subset of cells was the tumour-initiating population in 90% (nine out of ten) of melanomas tested. Transplantation of isolated CD271+ melanoma cells into engrafted human skin or bone in Rag2−/−¦Ãc−/− mice resulted in melanoma; however, melanoma did not develop after transplantation of isolated CD271− cells. We also show that in mice, tumours derived from transplanted human CD271+ melanoma cells were capable of metastatsis in vivo. CD271+ melanoma cells lacked expression of TYR, MART1 and MAGE in 86%, 69% and 68% of melanoma patients, respectively, which helps to explain why T-cell therapies directed at these antigens usually result in only temporary tumour shrinkage.
4. ¹ÇÐÎ̬±¬·¢ÂѰ×ά»¤Éñ¾¸Éϸ°û´¢±¸
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¡¾ÔÎÄժ¼¡¿Cell Stem Cell, Volume 7, Issue 1, 78-89, 2 July 2010
Signaling through BMPR-IA Regulates Quiescence and Long-Term Activity of Neural Stem Cells in the Adult Hippocampus
Helena Mira,Zoraida Andreu,Hoonkyo Suh
Neural stem cells (NSCs) in the adult hippocampus divide infrequently, and the molecules that modulate their quiescence are largely unknown. Here, we show that bone morphogenetic protein (BMP) signaling is active in hippocampal NSCs, downstream of BMPR-IA. BMPs reversibly diminish proliferation of cultured NSCs while maintaining their undifferentiated state. In vivo, acute blockade of BMP signaling in the hippocampus by intracerebral infusion of Noggin first recruits quiescent NSCs into the cycle and increases neurogenesis; subsequently, it leads to decreased stem cell division and depletion of precursors and newborn neurons. Consistently, selective ablation of Bmpr1a in hippocampal NSCs, or inactivation of BMP canonical signaling in conditional Smad4 knockout mice, transiently enhances proliferation but later leads to a reduced number of precursors, thereby limiting neuronal birth. BMPs are therefore required to balance NSC quiescence/proliferation and to prevent loss of the stem cell activity that supports continuous neurogenesis in the mature hippocampus.
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