356 research outputs found
Age work in organizations: maintaining and disrupting institutionalized understandings of higher age
Age diversity research calls for new approaches in explaining the persistence of age inequalities, which integrate different levels of analysis and display greater context sensitivity. Concurrently, neoinstitutionalist research interested in social inequalities calls for merging institutional theory with critical perspectives and to account for issues of power. In this study, we address the calls of both research streams through developing the concept of âage workâ: the institutional work actors undertake on age as a social institution. Applying our novel concept to a multi-actor study of four German organizations known for their age management, we come across a counterintuitive insight regarding actorsâ age work: maintaining stereotypical age images can serve to counter age inequalities, whereas deconstructing age images can reinforce age inequalities. The multi-actor perspective of our study allows us to categorize different forms of power-laden and interest-driven age work and to portray the reproduction of age inequalities as a result of actorsâ age work, embedded in different contexts and complex power relations. Comparing employeesâ forms of age work across sectors and organizations, we detail how notions of masculinity as well as income and job security shaped the categorized forms of age work
Interaction of CO and O<sub>2</sub> with Pt Studied by Field Ion Appearance Energy Spectroscopy
Using field ion appearance energy spectroscopy we have examined the interaction of CO and 02 with stepped platinum surfaces in the presence of electrostatic fields ranging between 10 and 20 V/nm. Mass-to-charge resolved retarding potential analyses have been carried out for single sites of [001] and [111]-oriented Pt field emitter exposed to a continuous flow of CO and 02. Applying a thermionic cycle, binding energies of molecularly adsorbed CO and O2, were derived from the appearance energies of field desorbed CO+ and O+2 . The data reveal an effect of the high field on the molecule-surface interaction, which is most pronounced for COPt(111) steps. Implications for FIM studies of catalytic CO and H2, oxidation reactions are discussed
Voorlichting en begeleiding bij de studie- en beroepskeuze en de rol van arbeidsmarktinformatie.
Erratum:BubR1 allelic effects drive phenotypic heterogeneity in mosaic-variegated aneuploidy progeria syndrome (Journal of Clinical Investigation (2020) 130:1 (171-188) DOI: 10.1172/JCI126863)
During the preparation of this manuscript, the same sample was inadvertently included for the +/L1002P and +/â images in Figure 2E. The authors were able to use the original samples to prepare a corrected version. The correct figure is below. The description in Methods for this panel has also been corrected, as below: To assess the mitotic index of spontaneous lymphatic tumors, mitotic cells were visualized by IF labelling of at least 1 paraffin section for pHH3 (EMD Millipore, catalog 06-570), as described (6, 46). The online version of the article has been updated with the corrected information. The authors regret the errors
BubR1 allelic effects drive phenotypic heterogeneity in mosaic-variegated aneuploidy progeria syndrome
Mosaic-variegated aneuploidy (MVA) syndrome is a rare childhood disorder characterized by biallelic BUBR1, CEP57, or TRIP13 aberrations; increased chromosome missegregation; and a broad spectrum of clinical features, including various cancers, congenital defects, and progeroid pathologies. To investigate the mechanisms underlying this disorder and its phenotypic heterogeneity, we mimicked the BUBR1(L1012P) mutation in mice (BubR1(L1002P)) and combined it with 2 other MVA variants, BUBR1(X753) and BUBR1(H), generating a truncated protein and low amounts of wild-type protein, respectively. Whereas BubR1(X753/L1002P) and BubR1(H/X753) mice died prematurely, BubR1(H/L1002P) mice were viable and exhibited many MVA features, including cancer predisposition and various progeroid phenotypes, such as short lifespan, dwarfism, lipodystrophy, sarcopenia, and low cardiac stress tolerance. Strikingly, although these mice had a reduction in total BUBR1 and spectrum of MVA phenotypes similar to that of BubR1(H/H) mice, several progeroid pathologies were attenuated in severity, which in skeletal muscle coincided with reduced senescence-associated secretory phenotype complexity. Additionally, mice carrying monoallelic BubR1 mutations were prone to select MVA-related pathologies later in life, with predisposition to sarcopenia correlating with mTORC1 hyperactivity. Together, these data demonstrate that BUBR1 allelic effects beyond protein level and aneuploidy contribute to disease heterogeneity in both MVA patients and heterozygous carriers of MVA mutations
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration
Mutations in the gene coding for Sequestosome 1 (SQSTM1) have been genetically associated with amyotrophic lateral sclerosis (ALS) and Paget disease of bone. In the present study, we analyzed the SQSTM1 coding sequence for mutations in an extended cohort of 1,808 patients with frontotemporal lobar degeneration (FTLD), ascertained within the European Early-Onset Dementia consortium. As control dataset, we sequenced 1,625 European control individuals and analyzed whole-exome sequence data of 2,274 German individuals (total n = 3,899). Association of rare SQSTM1 mutations was calculated in a meta-analysis of 4,332 FTLD and 10,240 control alleles. We identified 25 coding variants in FTLD patients of which 10 have not been described. Fifteen mutations were absent in the control individuals (carrier frequency < 0.00026) whilst the others were rare in both patients and control individuals. When pooling all variants with a minor allele frequency < 0.01, an overall frequency of 3.2 % was calculated in patients. Rare variant association analysis between patients and controls showed no difference over the whole protein, but suggested that rare mutations clustering in the UBA domain of SQSTM1 may influence disease susceptibility by doubling the risk for FTLD (RR = 2.18 [95 % CI 1.24-3.85]; corrected p value = 0.042). Detailed histopathology demonstrated that mutations in SQSTM1 associate with widespread neuronal and glial phospho-TDP-43 pathology. With this study, we provide further evidence for a putative role of rare mutations in SQSTM1 in the genetic etiology of FTLD and showed that, comparable to other FTLD/ALS genes, SQSTM1 mutations are associated with TDP-43 pathology
The Vehicle, Spring 1981
Vol. 22, No. 2
Table of Contents
Old Farmers at the Arcade CafeJohn Stockmanpage 4
ConfettiCathy Georgepage 6
Ode to a Corned Beef SandwichJeff Bennettpage 6
The Ice on Kirschner\u27s CreekScott Fishelpage 7
Love Poem to LindaJohn Stockmanpage 7
Grandfather\u27s PortraitJames Marshpage 8
The MassageKathleen Alakspage 9
A Driving ForceSandy Youngpage 10
King DandelionNancy Siebenpage 12
One Afternoon - Contemplating HouseworkKelli Sanderpage 13
Tent WallsAndy Sudkamppage 14
The SentinelElise Hempelpage 16
Daddy\u27s AftershaveJeff Bennettpage 16
The WeddingChris Goerlichpage 17
UntitledCarol Hansenpage 17
Treasures in the YardScott Fishelpage 18
Hitchhiker\u27s BootsAndy Sudkamppage 20
The RaffleLaura Henrypage 21
A Walk at NightJudi Jinespage 24
Morning in the DumpJeff Bennettpage 24
In Praise of Chocolate Ice CreamJohn Stockmanpage 25
Summer on the Isle of PalmsElisabeth Cristpage 26
The WaveHerbert S. Demminpage 27
RememberingJohn Kleinsteiberpage 27
PotatoJohn Stockmanpage 28
Late ShowChris Goerlichpage 30
Love in Him - JoeDebbie Klinnertpage 31
ShoeScott Fishelpage 35
The DrinkerBob Huntpage 36
The WidowGeorge Ndu Igbudupage 37
ElectricityScott Fishelpage 37
Hatchet JackB.L. Davidsonpage 39
Walking Home LateJohn Stockmanpage 41
NovemberCindy Hubbarttpage 41
On the BusLaura Henrypage 42
HaikuJames Marshpage 43
SpillwayGloria Rhoadspage 43
Art
Cover design by Linda Fraembs
PhotographRobin Scholzpage 3
PhotographRobin Scholzpage 5
PhotographMichelle Glassmeyerpage 15
PhotographRobert Schinaglpage 19
PhotographTom Robertspage 38
PhotographRobert Schinaglpage 44https://thekeep.eiu.edu/vehicle/1039/thumbnail.jp
Serratia marcescens internalization and replication in human bladder epithelial cells
BACKGROUND: Serratia marcescens, a frequent agent of catheterization-associated bacteriuria, strongly adheres to human bladder epithelial cells in culture. The epithelium normally provides a barrier between lumal organisms and the interstitium; the tight adhesion of bacteria to the epithelial cells can lead to internalization and subsequent lysis. However, internalisation was not shown yet for S. marcescens strains. METHODS: Elektronmicroscopy and the common gentamycin protection assay was used to assess intracellular bacteria. Via site directed mutagenesis, an hemolytic negative isogenic Serratia strain was generated to point out the importance of hemolysin production. RESULTS: We identified an important bacterial factor mediating the internalization of S. marcescens, and lysis of epithelial cells, as the secreted cytolysin ShlA. Microtubule filaments and actin filaments were shown to be involved in internalization. However, cytolysis of eukaryotic cells by ShlA was an interfering factor, and therefore hemolytic-negative mutants were used in subsequent experiments. Isogenic hemolysin-negative mutant strains were still adhesive, but were no longer cytotoxic, did not disrupt the cell culture monolayer, and were no longer internalized by HEp-2 and RT112 bladder epithelial cells under the conditions used for the wild-type strain. After wild-type S. marcescens became intracellular, the infected epithelial cells were lysed by extended vacuolation induced by ShlA. In late stages of vacuolation, highly motile S. marcescens cells were observed in the vacuoles. S. marcescens was also able to replicate in cultured HEp-2 cells, and replication was not dependent on hemolysin production. CONCLUSION: The results reported here showed that the pore-forming toxin ShlA triggers microtubule-dependent invasion and is the main factor inducing lysis of the epithelial cells to release the bacteria, and therefore plays a major role in the development of S. marcescens infections
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