596 resultados para Ufer, Clarence
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Proteinase inhibitor I (Inh I) and proteinase inhibitor II (Inh II) from potato tubers are effective proteinase inhibitors of chymotrypsin and trypsin. Inh I and Inh II were shown to suppress irradiation-induced transformation in mouse embryo fibroblasts suggesting that they possess anticarcinogenic characteristics. We have previously demonstrated that Inh I and Inh II could effectively block UV irradiation-induced activation of transcription activator protein 1 (AP-1) in mouse JB6 epidermal cells, which mechanistically may explain their anticarcinogenic actions. In the present study, we investigated the effects of Inh I and Inh II on the expression and composition pattern of the AP-1 complex following stimulation by UV B (UVB) irradiation in the JB6 model. We found that Inh I and Inh II specifically inhibited UVB-induced AP-1, but not NFκB, activity in JB6 cells. Both Inh I and Inh II up-regulated AP-1 constituent proteins, JunD and Fra-2, and suppressed c-Jun and c-Fos expression and composition in bound AP-1 in response to UVB stimulation. This regulation of the AP-1 protein compositional pattern in response to Inh I or Inh II may be critical for the inhibition of UVB-induced AP-1 activity by these agents found in potatoes.
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Systemin-mediated defense signaling in tomato (Lycopersicon esculentum) plants is analogous to the cytokine-mediated inflammatory response in animals. Herein, we report that the initiation of defense signaling in suspension-cultured cells of Lycopersicon peruvianum by the peptide systemin, as well as by chitosan and β-glucan elicitor from Phytophtora megasperma, is inhibited by the polysulfonated naphtylurea compound suramin, a known inhibitor of cytokine and growth factor receptor interactions in animal cells. Using a radioreceptor assay, we show that suramin interfered with the binding of the systemin analog 125I-Tyr-2,Ala-15-systemin to the systemin receptor with an IC50 of 160 μM. Additionally, labeling of the systemin receptor with a photoaffinity analog of systemin was inhibited in the presence of suramin. Receptor-mediated tyrosine phosphorylation of a 48-kDa mitogen-activated protein kinase and alkalinization of the medium of suspension-cultured cells in response to systemin and carbohydrate elicitors were also inhibited by suramin. The inhibition of medium alkalinization by suramin was reversible in the presence of high concentrations of systemin and carbohydrate elicitors. Calyculin A and erythrosin B, intracellular inhibitors of phosphatases and plasma membrane proton ATPases, respectively, both induce medium alkalinization, but neither response was inhibited by suramin. The polysulfonated compound heparin did not inhibit systemin-induced medium alkalinization. NF 007, a suramin derivative, induced medium alkalinization, indicating that neither NF 007 nor heparin interact with elicitor receptors like suramin. The data indicate that cell-surface receptors in plants show some common structural features with animal cytokine and growth factor receptors that can interact with suramin to interfere with ligand binding.
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Plants that have been wounded by insects or other herbivores may be more susceptible to infection by adventitious microbes. Wound-induced signal molecules, which serve to induce responses in the plant that retard further feeding, might also act to prepare a plant for possible pathogen attack. We have examined the effect of a wound-generated systemic messenger (systemin) on a pathogen-stimulated defense-response marker, the oxidative burst. We observed that neither systemin nor its inactive analog (A-17) was able to directly induce H2O2 biosynthesis in suspension-cultured tomato (Lycopersicon esculentum L.) cells, regardless of the duration of exposure of the cells to the two peptides. Similarly, neither systemin nor A-17 was capable of modifying an oligogalacturonide-elicited oxidative burst, as long as elicitor addition occurred within minutes of treatment with systemin or A-17. In contrast, preexposure of the cell cultures to systemin (but not to A-17) led to a time-dependent enhancement of the oligogalacturonide-elicited oxidative burst. By 12 h of exposure, the H2O2 biosynthetic capacity of systemin-treated cells exceeded that of the control cells by a factor of 16 ± 2. A similar up-regulation by systemin of a mechanically stimulated oxidative burst was also observed. Because the systemin-induced augmentation in oxidant synthesis is quantitatively prevented by coincubation with 2 μm cycloheximide, and because the oxidative burst of oligogalacturonic acid-elicited control cells (no systemin exposure) is unaffected by preincubation with cycloheximide, we conclude that systemin enhancement of the tomato-cell oxidative burst requires protein synthesis.
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The effects of abscisic acid (ABA) on the accumulation of proteinase inhibitors I (Inh I) and II (Inh II) in young, excised tomato (Lycopersicon esculentum L.) plants were investigated. When supplied to excised plants through the cut stems, 100 μm ABA induced the activation of the ABA-responsive le4 gene. However, under the same conditions of assay, ABA at concentrations of up to 100 μm induced only low levels of proteinase-inhibitor proteins or mRNAs, compared with levels induced by systemin or jasmonic acid over the 24 h following treatment. In addition, ABA only weakly induced the accumulation of mRNAs of several other wound-response proteins. Assays of the ABA concentrations in leaves following wounding indicated that the ABA levels increased preferentially near the wound site, suggesting that ABA may have accumulated because of desiccation. The evidence suggests that ABA is not a component of the wound-inducible signal transduction pathway leading to defense gene activation but is likely involved in the general maintenance of a healthy plant physiology that facilitates a normal wound response.
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Excavations were carried out in a Late Palaeolithic site in the community of Bad Buchau-Kappel between 2003 and 2007. Archaeological investigations covered a total of more than 200 m**2. This site is the product of what likely were multiple occupations that occurred during the Late Glacial on the Federsee shore in this location. The site is situated on a mineral ridge that projected into the former Late Glacial lake Federsee. This beach ridge consists of deposits of fine to coarse gravel and sand and was surrounded by open water, except for a connection to the solid shore on the south. A lagoon lay between the hook-shaped ridge and the shore of the Federsee. This exposed location provided optimal access to the water of the lake. In addition, the small lagoon may have served as a natural harbor for landing boats or canoes. Sedimentological and palynological investigations document the dynamic history of the location between 14,500 and 11,600 years before present (cal BP). Evidence of the deposition of sands, gravels and muds since the Bølling Interstadial is provided by stratigraphic and palynological analyses. The major occupation occurred in the second half of the Younger Dryas period. Most of the finds were located on or in the sediments of the ridge; fewer finds occurred in the surrounding mud, which was also deposited during the Younger Dryas. Direct dates on some bone fragments, however, demonstrate that intermittent sporadic occupations also took place during the two millennia of the Meiendorf, Bølling, and Allerød Interstadials. These bones were reworked during the Younger Dryas and redeposited in the mud. A 14C date from one bone of 11,600 years ago (cal BP) places the Late Palaeolithic occupation of the ridge at the very end of the Younger Dryas, which is in agreement with stratigraphic observations. Stone artifacts, numbering 3,281, comprise the majority of finds from the site. These include typical artifacts of the Late Palaeolithic, such as backed points, short scrapers, and small burins. There are no bipointes or Malaurie-Points, which is in accord with the absolute date of the occupation. A majority of the artifacts are made from a brown chert that is obtainable a few kilometers north of the site in sediments of the Graupensandrinne. Other raw materials include red and green radiolarite that occur in the fluvioglacial gravels of Oberschwaben, as well as quartzite and lydite. The only non-local material present is a few artifacts of tabular chert from the region near Kelheim in Bavaria. A unique find consists of two fragments of a double-barbed harpoon made of red deer antler, which was found in the Younger Dryas mud. It is likely, but not certain, that this find belongs to the same assemblage as the numerous stone artifacts. Although not numerous, animal bones were also found in the excavations. Most of them lay in sediments of the Younger Dryas, but several 14C dates place some of these bones in earlier periods, including the Meiendorf, Bølling, and Allerød Interstadials. These bones were reworked by water and redeposited in mud sediments during the Younger Dryas. As a result, it is difficult to attribute individual bones to particular chronological positions without exact dates. Species that could be identified include wild horse (Equus spec.), moose or elk (Alces alces), red deer (Cervus elaphus), roe deer (Capreolus capreolus), aurochs or bison (Bos spec.), wild boar (Sus scrofa), as well as birds and fish, including pike (Esox Lucius).
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Bibliography: p. [62]-64.
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Includes indexes.
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Bibliography: p. [341]-353.
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"Constitutes report no. 4 under contract no. 12-17-07-5-1651, June 24, 1976 (ERS-192-B-76)"
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Bibliography: p. [99]-101.
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Music: p. 225-252
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Campus viewed from the northwest, with Haven Hall and University Hall in foreground. Publication information: [Chicago, Ill.] : Everts & Stewart, 1874.
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Back Row: John Faulk, Jeff Long, T.J. Weist, Mike Debord, Greg Mattison, Bill Harris, Les Miles, Cam Cameron, Lloyd Carr, Bobby Morrison, Jim Herrmann, Fred Jackson, Bob Chmiel, Mike Gittleson, Phil Bromley, Paul Schmidt, Todd Jager
7th Row: Scott Rogow, Ed O'Dowd, Dorey Hicks, Lance Satterthwaite, Thom Holden (27), Josh Cockrell (74), Sean Parini (89), Jace Morgan (38), Brian Griese (14), Scot Loeffler (15), Jeff Springer (71), Brian Williams (19), Colby Keefer (29), Mike Hynes (25), John McNulty, Jeff Travis, Jason Cole, Brian Letcher
6th Row: Kyle Timkin, Jim Plocki, Nate Delong (39), J.J. Brown (43), William Carr (96), Pierre Cooper (88), Damon Denson (99), Dayna Overton (4), Jon Ritchie (40), Clarence Thompson (17), Mike Elston, Glen Steele, John Partchenko, Trevor Pryce, Joe Ries, Bob Bland, Brian Hagens, Lee Taggart
5th Row: Scott Draper, Paul Peristeris (99), Brent Blackwell (24), Tim Biakabutuka (21), Zach Adami (68), Damon Jones (85), Julian Norment (50), Tyrone Noble (42), Steve King (27), Steve Evans (92), Mike Mangan (71), Jared Lancer (39), Rob Swett (44), Seth Smith (86), Ernest Sanders (49), Ben Huff (53), George Howell (51), Schemy Schembechler
4th Row: Woody Hankins (23), Mike Vanderbeek (45), Harold Goodwin (56), Shawn Collins (32), Deollo Anderson (32), Eric Wendt (65), Marc Bolach (70), Mercury Hayes (9), Chuck Winters (35), Amani Toomer (18), Jon Runyan (69), Thomas Guynes (75), Rod Payne (52), Jarrett Irons (37), Jean Angus Charles (34), Kerwin Waldroup (59), Remy Hamilton (19)
3rd Row: Zach Freedman (24), Chad Petterson (43), Todd Richards (83), Ante Skorput (62), Jason Carr (13), Joe Marinaro (73), Che' Foster (33), Paul Barry (78), Trent Zenkewicz (76), Jay Riemersma (16), Mike Sullivan (61), Felman Malveaux (84), Ed Davis (26), Rob Vander Leest (58), Jeff Zaeske (34), Ty Law (22), Gary Moeller
2nd Row: Sergio Gasperoni (44), Erik Lovell (38), John Jaeckin (82), Marcus Walker (46), Shawn Miller (57), Matt Dyson (91), Todd Collins (10), Steve Morrison (36), Tony Henderson (79), Greg McThomas (41), Bobby Powers (95), Deon Johnson (28), Jason Horn (94), Trezelle Jenkins (77), Tyrone Wheatley (6)
Front Row: Chris Stapleton (18), Jesse Johnson (30), Ron Buff (25), Walter Smith (2), Derrick Alexander (1), Ninef Aghakan (90), Shonte Peoples (3), Ricky Powers (12), Marc Milia (67), Buster Stanley (60), Alfie Burch (8), Gannon Dudlar (55) Tony Blankenship (31), Steve Rekowski (66), Peter Elezovic (29)
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Back Row: Todd Jager, Paul Schmidt, Bill Shinavier, Mike Gittleson, Kit Cartwright, Greg Mattison, Fred Jackson, Les Miles, Lloyd Carr, Bill Harris, Bobby Morrison, Mike DeBord, Jim Herrmann, John McNulty, John Milligan, Jon Falk, Phil Bromley, Steve Connelly
8th Row: Brian Letscher, Brian Townsend, Ed O'Dowd, Jason Cole, Jim Plocki, Andy Riegler, Chris Singletary, Jon Jansen, Jeff Holtry, Marcus Ray, Anthony Williams, Tim Laws, Bob Bland, Brian Hagens, Gordon Grace, Shemy Schembechler, Scott Draper
7th Row: Darren Petterson, Ed Kiser, Jay Feely, Noah Parker, Juaquin Feazell, Clint Copenhaver, Tyrone Butterfield, Kraig Baker, Todd Brooks, Mark Campbell, Scott Dreisbach, Chris Floyd, Chris Howard, Matt Sygo, Nate Miller, Terrence Quinn, Clarence Thompson
6th Row: Andre Weathers, Sam Sword, Josh Cockrell, Thomas Mondry, Jace Morgan, Sean Parini, Nate DeLong, Brent Blackwell, Brian Griese, Jeff Springer, Lance Sanders, Colby Keefer, Matt DeYoung, Rasheed Simmons, Jerame Tuman, Earnest Sanders
5th Row: Head Coach Gary Moeller, Scott Loeffler, George Howell, Will Carr, Rob Swett, Jon Ritchie, Tim Biakabutuka, Zach Adami, Damon Denson, Pierre Cooper, Trevor Pryce, Mike Elston, Ben Huff, Seth Smith, Dr. Gerald O'Connor, Dr. Edward Wojtys
4th Row: Joe Ries, Mike Hynes, Rod Payne, Julian Norment, Tyrone Noble, Amani Toomer, Kerwin Waldroup, Remy Hamilton, Bryan Williams, Jared Lancer, Paul Peristeris, Glen Steele, Paul Berry
3rd Row: John Partchenko, Woody Hankins, Jean-Agnus Charles, Jarrett Irons, Eric Wendt, Steve Evans, Thomas Guynes, Jon Runyan, Mark Bolach, Harold Goodwin, Ty Law, Steve King, Mike Vanderbeek
2nd Row: Mercury Hayes, Chuck Winters, Todd Richards, Chad Petterson, Ante Skorput, Joe Marinaro, Trent Zenkewicz, Jason Horn, Trezelle Jenkins, Mike Sullivan, Rob Vander Leest, Erik Lovell, Deollo Anderson
Front Row: Bobby Powers, Deon Johnson, Tony Henderson, Walter Smith, Steve Morrison, Todd Collins, Matt Dyson, Tyrone Wheatley, Jay Riemersma, Eddie Davis, Jason Carr, Che' Foster