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21.
IGF1 receptor expression protects against microenvironmental stress found in the solid tumor 总被引:7,自引:0,他引:7
The insulin-like growth factor 1 receptor (IGF1R) is a tyrosine kinase, transmembrane receptor expressed in most body tissues and required for normal growth of cells. In cell culture, overexpression of the receptor has been shown to promote transformation and enhance cell survival in response to selected cytotoxic agents. As tumors develop, abnormalities in vascularization lead to a heterogeneous environment that includes areas of hypoxia, low pH and low glucose. Here we report that the overexpression of the IGF1R promotes increased survival in cells exposed to hypoxia, low pH and low glucose. Furthermore, cells lacking the receptor due to targeted disruption of the IGF1R gene do not survive as well as normal cells in such conditions. In addition, we find that cells can activate the IGF1R gene promoter in response to these conditions, and immunoblot analyses show increased receptor protein levels in cell exposed to hypoxia. Our results suggest a pathway of cancer cell adaptation to the tumor microenvironment in which conditions of the environment may induce expression of IGF1R, and this subsequent overexpression of the receptor may increase cell survival in such conditions. 相似文献
22.
Estrogen induces a rapid increase in microvascular permeability in the rodent uterus, leading to stromal edema and a marked increase in uterine wet weight. This edema is believed to create an environment optimal for the growth and remodeling of the endometrium in preparation for implantation and pregnancy. Increased endometrial microvascular permeability also occurs in conjunction with implantation. Estrogen-induced uterine edema is immediately preceded by an increase in the expression of vascular endothelial growth factor (VEGF), a potent stimulator of microvascular permeability. The objective of this study was to determine to what degree immunoneutralization of VEGF would interfere with a) estradiol-induced uterine edema and b) pregnancy. In the first set of experiments, immature female rats were injected with either VEGF antiserum or normal rabbit serum (NRS) prior to 17beta-estradiol treatment. Rats treated with estradiol alone showed a 57% increase in uterine wet weight at 6 h compared with controls. Injection of 200 or 300 micro l of VEGF antiserum reduced the response to only 20% and 10% above controls, respectively. In the second set of experiments, young adult female mice were treated with 100 micro l of either VEGF antiserum or NRS at 1200 h on the fourth day after mating. NRS-treated mice had normal pregnancies. VEGF antiserum, however, completely blocked pregnancy. When VEGF antiserum-treated females were examined on Day 5 for the presence of implantation sites, none were found. These results show that a) VEGF is the major mediator of estrogen-induced increase in uterine vascular permeability and b) VEGF-induced edema is absolutely essential for implantation to take place. 相似文献
23.
24.
Extensor tendon: anatomy, injury, and reconstruction 总被引:5,自引:0,他引:5
Rockwell WB Butler PN Byrne BA 《Plastic and reconstructive surgery》2000,106(7):1592-603; quiz 1604, 1673
Although seemingly simple in its anatomy and function, the extensor mechanism of the hand is actually a complex set of interlinked muscles, tendons, and ligaments. A thorough understanding of the extensor anatomy is required to understand the consequences of injury at various levels. Reconstructive options must restore normal function. Whereas primary repair of anatomic structures is frequently possible in acute injury, it is rarely possible in chronic situations. Technically exacting procedures may be necessary to restore function. 相似文献
25.
The detection of vegetational change by multitemporal analysis of LANDSAT data: the effects of goose foraging 总被引:3,自引:1,他引:2
1 The North American mid-continent population of lesser snow geese now exceeds 3 million birds and the population is increasing in the order of 7% per annum. The foraging activities of the birds on Arctic breeding grounds are leading to loss of vegetation and habitat destruction, particularly in coastal areas bordering the Hudson and James Bays.
2 Multitemporal analysis of LANDSAT data has been carried out to detect vegetational change from 1973 to 1993 at La Pérouse Bay and its vicinity, the site of a breeding colony of snow geese.
3 Difference vegetation images (DVI) (difference between infra-red and red images) were prepared from images obtained in late summer in 1973, 1984 and 1993, in order to enhance vegetation density. Pair-wise differences were calculated between these DVI images, which resulted in three, secondary, classified images. Classification of the three secondary images (1973–84, 1984–93, 1973–93) yielded three well-defined classes: water, vegetation decline and no change in vegetation.
4 Histogram counts gave the following values for areas of vegetation decline: 1973–84, 1026 ha; 1984–93, 1428 ha; 1973–93, 2454 ha.
5 The loss of vegetation and the destruction of habitat are discussed in relation to the foraging activities of the expanding goose population. 相似文献
2 Multitemporal analysis of LANDSAT data has been carried out to detect vegetational change from 1973 to 1993 at La Pérouse Bay and its vicinity, the site of a breeding colony of snow geese.
3 Difference vegetation images (DVI) (difference between infra-red and red images) were prepared from images obtained in late summer in 1973, 1984 and 1993, in order to enhance vegetation density. Pair-wise differences were calculated between these DVI images, which resulted in three, secondary, classified images. Classification of the three secondary images (1973–84, 1984–93, 1973–93) yielded three well-defined classes: water, vegetation decline and no change in vegetation.
4 Histogram counts gave the following values for areas of vegetation decline: 1973–84, 1026 ha; 1984–93, 1428 ha; 1973–93, 2454 ha.
5 The loss of vegetation and the destruction of habitat are discussed in relation to the foraging activities of the expanding goose population. 相似文献
26.
27.
Identifying prosurvival mechanisms in stressed neuronal cells would provide protective strategies to hinder neurodegeneration.
Recent evidence shows that vascular endothelial growth factor (VEGF), a well-established mitogen in endothelial cells, can
mediate neuroprotection against damaging insults through the activation of its cognate receptor VEGFR2. In addition, growth
factor receptor signaling pathways have been shown to crosstalk with cAMP-dependent Protein Kinase A (PKA) to protect neuronal
cells from harmful stimuli. Whether a relationship exists between VEGFR2 and PKA in mediating neuroprotection under stressful
conditions is unknown. Using SK-N-SH neuronal cells as a model system, we show that serum deprivation induces an upregulation
in VEGF and VEGFR2 that concomitantly serves as a prosurvival signaling pathway. Inhibitor studies revealed that PKA functioned
concurrently with VEGFR2 pathway to signal the activation of the extracellular signal-regulated protein kinases (ERK1/2) as
protection against caspase-3/7 activation and a subsequent cell death. The loss in cell viability induced by VEGFR2 and PKA
inhibition was prevented by caspase inhibition or overexpression of ERK1. Overexpression of the antiapoptotic protein Bcl-xL
also promoted survival when VEGFR2 function was blocked. However, the protection elicited by all three treatments were prevented
by the inclusion of a selective inhibitor of mitogen-activated protein kinase kinase (MEK), the upstream kinase that activates
ERK1/2. Taken together, these findings suggested that PKA and VEGFR2 converge at the MEK/ERK1/2 pathway to protect serum starved
neuronal cells from a caspase-dependent cell death.
Electronic supplementary material The online version of this article (doi:) contains supplementary material, which is available to authorized users. 相似文献
28.
Karen E. Sears Allison K. Bormet Alexander Rockwell Lisa E. Powers Lisa Noelle Cooper Matthew B. Wheeler 《Evolution & development》2011,13(6):533-541
Digit reduction has occurred in parallel in many mammalian lineages. However, despite this pattern's prevalence, the developmental mechanisms underlying mammalian digit reduction remain controversial. We therefore undertook a study of digit development in the pig (Sus scrofa), a mammal with reduced first, second, and fifth digits. Our results indicate that from its earliest formation, the pig limb bud is significantly narrower than that of the model pentadactyl mammal, mouse. Furthermore, the cartilage condensations of the pig's reduced digits are noticeably smaller than those of their nonreduced counterparts from the time of their formation. In addition, growth rates of pig digits are comparable, as are the patterns of cell death in developing pig and mouse limbs. Taken together, results suggest that pig's first, second, and fifth digits are primarily reduced through evolutionary modifications in the early developmental patterning of their limbs. Results of this study, coupled with those from study of limb development in other mammals, suggest that although major developmental reorganizations (e.g., complete digit or limb loss) during early limb development may be selected against, it may be common for more subtle evolutionary modifications in limb development (e.g., changes in relative digit size) to occur at this time. 相似文献
29.
Animal models for radiation injury, protection and therapy 总被引:1,自引:0,他引:1
Augustine AD Gondré-Lewis T McBride W Miller L Pellmar TC Rockwell S 《Radiation research》2005,164(1):100-109
Current events throughout the world underscore the growing threat of different forms of terrorism, including radiological or nuclear attack. Pharmaceutical products and other approaches are needed to protect the civilian population from radiation and to treat those with radiation-induced injuries. In the event of an attack, radiation exposures will be heterogeneous in terms of both dose and quality, depending on the type of device used and each victim's location relative to the radiation source. Therefore, methods are needed to protect against and treat a wide range of early and slowly developing radiation-induced injuries. Equally important is the development of rapid and accurate biodosimetry methods for estimating radiation doses to individuals and guiding clinical treatment decisions. Acute effects of high-dose radiation include hematopoietic cell loss, immune suppression, mucosal damage (gastrointestinal and oral), and potential injury to other sites such as the lung, kidney and central nervous system (CNS). Long-term effects, as a result of both high- and low-dose radiation, include dysfunction or fibrosis in a wide range of organs and tissues and cancer. The availability of appropriate types of animal models, as well as adequate numbers of animals, is likely to be a major bottleneck in the development of new or improved radioprotectors, mitigators and therapeutic agents to prevent or treat radiation injuries and of biodosimetry methods to measure radiation doses to individuals. 相似文献
30.
Seow HA Penketh PG Belcourt MF Tomasz M Rockwell S Sartorelli AC 《The Journal of biological chemistry》2004,279(30):31606-31612
The effects of the subcellular localization of overexpressed bioreductive enzyme NAD(P)H:quinone oxidoreductase 1 (NQO1) on the activity of the antineoplastic agent mitomycin C (MC) under aerobic and hypoxic conditions were examined. Chinese hamster ovary (CHO-K1/dhfr(-)) cells were transfected with NQO1 cDNA to produce cells that overexpressed NQO1 activity in the nucleus (148-fold) or the cytosol (163-fold) over the constitutive level of the enzyme in parental cells. Subcellular localization of the enzyme was confirmed using antibody-assisted immunofluorescence. Nuclear localization of transfected NQO1 activity increased the cytotoxicity of MC over that produced by overexpression in the cytosol under both aerobic and hypoxic conditions, with greater cytotoxicity being produced under hypoxia. The greater cytotoxicity of nuclear localized NQO1 was not attributable to greater metabolic activation of MC but instead was the result of activation of the drug in close proximity to its target, nuclear DNA. A positive relationship existed between the degree of MC-induced cytotoxicity and the number of MC-DNA adducts produced. The findings indicate that activation of MC proximal to nuclear DNA by the nuclear localization of transfected NQO1 increases the cytotoxic effects of MC regardless of the degree of oxygenation and support the concept that the mechanism of action of MC involves alkylation of DNA. 相似文献