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951.
Sequential augmentation reveals life history and suitable conditions for colonization of the rare mahogany mistletoe in South Florida 下载免费PDF全文
Janice A. Duquesnel Joyce Maschinski Robert McElderry George D. Gann Keith Bradley Ernest Cowan 《Restoration Ecology》2017,25(4):516-523
Successfully reintroducing rare plant populations to recover historical community composition may require multiple efforts and greater lengths of time than is typically devoted by researchers. To improve the probability of successful colonization and to learn about the life history of the regionally endangered mahogany mistletoe (Phoradendron rubrum) in the Florida Keys, United States, we conducted sequential augmentations for 10 years across two host tree sizes, two seed sources, and six recipient sites. Long‐term monitoring for 13 years revealed that sowing fresh seeds in dry periods from introduced versus wild plants onto small diameter trees (<20 cm diameter at breast height [dbh]) that had branch diameters 15–20 mm resulted in the greatest colonization success. An average of 38.7% of seeds germinated and 23.8% survived to 2015. Plant development was quite slow. Seeds required over 100 days to germinate, 1.6 years for cotyledon emergence, and over 4.7 years to produce fruit. We detected first recruitment nearly 8 years after installation. Population growth improved following multiple attempts and expanded spatial extent as is predicted by theory. Portions of the life cycle are undetectable and thus could give false indications of reintroduction success or failure. Achieving and documenting unequivocal success of this reintroduction has required over a decade. 相似文献
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Background
Trophoblast migration into maternal decidua is essential for normal pregnancy. It occurs in a defined time window, is spatially highly restricted, and is aberrant in some pathological pregnancies, but the control mechanisms are as yet ill-defined. At the periphery of the placenta, chorionic villi make contact with decidua to form specialised anchoring sites that feed interstitially migrating cytotrophoblast into the placental bed. 相似文献953.
Julia Reiriz Pontus C. Holm Jordi Alberch Ernest Arenas 《Developmental neurobiology》2002,50(4):291-304
The locus coeruleus (LC) is a major target of several neurodegenerative disorders, including Parkinson's and Alzheimer's diseases. However, very little is known of the trophic requirements of LC neurons. In the present work, we have studied the biological activity of neurotrophic factors from different families in E15 primary cultures of LC neurons. In agreement with previous results, neurotrophin‐3 (NT‐3) and also glial cell line‐ derived neurotrophic factor (GDNF) increased the number of embryonic LC noradrenergic neurons in the presence of serum. In serum‐free conditions, none of the factors tested, including NT‐3, GDNF, neurturin, basic fibroblast growth factor (bFGF), or bone morphogenetic protein‐2 (BMP‐2), promoted the survival of tyrosine hydroxylase (TH)‐immunoreactive neurons at 6 days in vitro. However, when BMP‐2 was coadministered with any of these factors the number of LC TH‐positive neurons increased twofold. Similar results were obtained by cotreatment of LC neurons with forskolin and NT‐3, bFGF, or BMP‐2. The strongest effect (a fourfold increase in the number of TH‐positive cells) was induced by cotreatment with forskolin, BMP‐2, and GDNF. Thus, our results show that LC neurons require multiple factors for their survival and development, and suggest that activation of LC neurons by bone morphogenetic proteins and cAMP plays a decisive role in conferring noradrenergic neuron responsiveness to several trophic factors. © 2002 Wiley Periodicals, Inc. J Neurobiol 50: 291–304, 2002; DOI 10.1002/neu.10034 相似文献
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Molecular and Cellular Biochemistry - 相似文献
955.
Murine homolog of SALL1 is essential for ureteric bud invasion in kidney development. 总被引:19,自引:0,他引:19
R Nishinakamura Y Matsumoto K Nakao K Nakamura A Sato N G Copeland D J Gilbert N A Jenkins S Scully D L Lacey M Katsuki M Asashima T Yokota 《Development (Cambridge, England)》2001,128(16):3105-3115
SALL1 is a mammalian homolog of the Drosophila region-specific homeotic gene spalt (sal); heterozygous mutations in SALL1 in humans lead to Townes-Brocks syndrome. We have isolated a mouse homolog of SALL1 (Sall1) and found that mice deficient in Sall1 die in the perinatal period and that kidney agenesis or severe dysgenesis are present. Sall1 is expressed in the metanephric mesenchyme surrounding ureteric bud; homozygous deletion of Sall1 results in an incomplete ureteric bud outgrowth, a failure of tubule formation in the mesenchyme and an apoptosis of the mesenchyme. This phenotype is likely to be primarily caused by the absence of the inductive signal from the ureter, as the Sall1-deficient mesenchyme is competent with respect to epithelial differentiation. Sall1 is therefore essential for ureteric bud invasion, the initial key step for metanephros development. 相似文献
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Bruce L. Riser Feridoon Najmabadi Bernard Perbal Jo Ann Rambow Melisa L. Riser Ernest Sukowski Herman Yeger Sarah C. Riser Darryl R. Peterson 《Journal of cell communication and signaling》2010,4(1):39-50
Prior work in the CCN field, including our own, suggested to us that there might be co-regulatory activity and function as part of the actions of this family of cysteine rich cytokines. CCN2 is now regarded as a major pro-fibrotic molecule acting both down-stream and independent of TGF-β1, and appears causal in the disease afflicting multiple organs. Since diabetic renal fibrosis is a common complication of diabetes, and a major cause of end stage renal disease (ESRD), we examined the possibility that CCN3 (NOV), might act as an endogenous negative regulator of CCN2 with the capacity to limit the overproduction of extracellular matrix (ECM), and thus prevent, or ameliorate fibrosis. We demonstrate, using an in vitro model of diabetic renal fibrosis, that both exogenous treatment with CCN3 and transfection with the over-expression of the CCN3 gene in mesangial cells markedly down-regulates CCN2 activity and blocks ECM over-accumulation stimulated by TGF-β1. Conversely, TGF-β1 treatment reduces endogenous CCN3 expression and increases CCN2 activity and matrix accumulation, indicating an important, novel yin/yang effect. Using the db/db mouse model of diabetic nephropathy, we confirm the expression of CCN3 in the kidney, with temporal localization that supports these in vitro findings. In summary, the results corroborate our hypothesis that one function of CCN3 is to regulate CCN2 activity and at the concentrations and conditions used down-regulates the effects of TGF-β1, acting to limit ECM turnover and fibrosis in vivo. The findings suggest opportunities for novel endogenous-based therapy either by the administration, or the upregulation of CCN3. 相似文献
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