44 research outputs found
High-Throughput Screening of Australian Marine Organism Extracts for Bioactive Molecules Affecting the Cellular Storage of Neutral Lipids
- Author
- A Schlegel
- AA Salim
- AE Carpenter
- Angela A. Salim
- BE Cham
- Ben C.B. Ko
- D Gilham
- FR Maxfield
- Frank Fontaine
- GP Jones
- H Tomoda
- H Yamazaki
- Harriet P. Lo
- HH Hatt
- I Namatame
- I Namatame
- J Hermoso
- J McLauchlan
- James Rae
- JK Zehmer
- KM Szymanski
- L Kuerschner
- M Andre
- M Bluher
- M Westerfield
- MM Samsa
- MS Gauthier
- MS Kim
- N Anderson
- N Hasegawa
- N Koyama
- N Mayorek
- N Mayorek
- N Morral
- O Morand
- R Obata
- R Uchida
- Robert G. Parton
- Robert J. Capon
- RV Farese Jr
- S Martin
- S Martin
- S Martin
- Sally Martin
- T Ohshiro
- V Grimard
- W Fei
- Y Guo
- Y Liu
- Publication venue
- Public Library of Science
- Publication date
- 08/08/2011
- Field of study
Mammalian cells store excess fatty acids as neutral lipids in specialised organelles called lipid droplets (LDs). Using a simple cell-based assay and open-source software we established a high throughput screen for LD formation in A431 cells in order to identify small bioactive molecules affecting lipid storage. Screening an n-butanol extract library from Australian marine organisms we identified 114 extracts that produced either an increase or a decrease in LD formation in fatty acid-treated A431 cells with varying degrees of cytotoxicity. We selected for further analysis a non-cytotoxic extract derived from the genus Spongia (Heterofibria). Solvent partitioning, HPLC fractionation and spectroscopic analysis (NMR, MS) identified a family of related molecules within this extract with unique structural features, a subset of which reduced LD formation. We selected one of these molecules, heterofibrin A1, for more detailed cellular analysis. Inhibition of LD biogenesis by heterofibrin A1 was observed in both A431 cells and AML12 hepatocytes. The activity of heterofibrin A1 was dose dependent with 20 ”M inhibiting LD formation and triglyceride accumulation by âŒ50% in the presence of 50 ”M oleic acid. Using a fluorescent fatty acid analogue we found that heterofibrin A1 significantly reduces the intracellular accumulation of fatty acids and results in the formation of distinct fatty acid metabolites in both cultured cells and in embryos of the zebrafish Danio rerio. In summary we have shown using readily accessible software and a relatively simple assay system that we can identify and isolate bioactive molecules from marine extracts, which affect the formation of LDs and the metabolism of fatty acids both in vitro and in vivo
Rab18 Dynamics in Adipocytes in Relation to Lipogenesis, Lipolysis and Obesity
- Author
- A Lutcke
- A Tchernof
- Alberto Diaz-Ruiz
- AR Kimmel
- B Razani
- BL Grosshans
- BL Wajchenberg
- C Hurtado Del Pozo
- CM Jenkins
- D Langin
- D Williams
- DA Brown
- DJ Klemm
- DJ Murphy
- DL Brasaemle
- DL Brasaemle
- E Lai
- F Momboisse
- FJ Ortega
- Francisco Gracia-Navarro
- Francisco Tinahones
- G Baldini
- G Baldini
- G Fruhbeck
- G Montero-Moran
- Gema FrĂŒhbeck
- GF Lewis
- H Shi
- H Shibata
- J Berndt
- JE Pessin
- JK Zehmer
- JM Goodman
- JM Ntambi
- José López-Miranda
- K Jaworski
- L Kuerschner
- M Ahmadian
- M Ahmadian
- M Fukuda
- M Kanzaki
- M Lafontan
- M Zerial
- Maria M. MalagĂłn
- Marian Ludgate
- Marina R. Pulido
- NA Ducharme
- NE Wolins
- NE Wolins
- NE Wolins
- NE Wolins
- P Cornelius
- P Liu
- P Trayhurn
- R Bartz
- R Vazquez-Martinez
- Rafael VĂĄzquez-MartĂnez
- RE Duncan
- S Cermelli
- S Genuth
- S Kersten
- S Kralisch
- S Martin
- S Martin
- S Ozeki
- SJ Guest
- Socorro Garcia-Navarro
- SY Dejgaard
- T Fujimoto
- T Tsuboi
- T Tsuboi
- W Yu
- Y Fujimoto
- Y Xie
- Yolanda Jiménez-Gómez
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2011
- Field of study
Lipid droplets (LDs) are organelles that coordinate lipid storage and mobilization, both processes being especially important in cells specialized in managing fat, the adipocytes. Proteomic analyses of LDs have consistently identified the small GTPase Rab18 as a component of the LD coat. However, the specific contribution of Rab18 to adipocyte function remains to be elucidated. Herein, we have analyzed Rab18 expression, intracellular localization and function in relation to the metabolic status of adipocytes. We show that Rab18 production increases during adipogenic differentiation of 3T3-L1 cells. In addition, our data show that insulin induces, via phosphatidylinositol 3-kinase (PI3K), the recruitment of Rab18 to the surface of LDs. Furthermore, Rab18 overexpression increased basal lipogenesis and Rab18 silencing impaired the lipogenic response to insulin, thereby suggesting that this GTPase promotes fat accumulation in adipocytes. On the other hand, studies of the ÎČ-adrenergic receptor agonist isoproterenol confirmed and extended previous evidence for the participation of Rab18 in lipolysis. Together, our data support the view that Rab18 is a common mediator of lipolysis and lipogenesis and suggests that the endoplasmic reticulum (ER) is the link that enables Rab18 action on these two processes. Finally, we describe, for the first time, the presence of Rab18 in human adipose tissue, wherein the expression of this GTPase exhibits sex- and depot-specific differences and is correlated to obesity. Taken together, these findings indicate that Rab18 is involved in insulin-mediated lipogenesis, as well as in ÎČ-adrenergic-induced lipolysis, likely facilitating interaction of LDs with ER membranes and the exchange of lipids between these compartments. A role for Rab18 in the regulation of adipocyte biology under both normal and pathological conditions is proposed
Quantitative Analysis of Lipid Droplet Fusion: Inefficient Steady State Fusion but Rapid Stimulation by Chemical Fusogens
- Author
- A Lass
- A Pol
- A Pol
- C Hoffmann
- C Valetti
- D Binns
- D Zweytick
- DA Brown
- DJ Murphy
- DL Brasaemle
- E Smirnova
- EJ Blanchette-Mackie
- G Kellner-Weibel
- H Miyoshi
- IT Mak
- J Bain
- J Bain
- Jean Gruenberg
- KW Surewicz
- L Kuerschner
- LG Herbette
- M Nagayama
- MA Welte
- MA Welte
- MK Olsen
- N Vereshchagina
- NE Wolins
- P Bostrom
- P Bostrom
- P Liu
- P Targett-Adams
- PL Chong
- RG Sturmey
- Robert G. Parton
- S De Carlo
- S Fukumoto
- S Le Lay
- S Martin
- S Murphy
- S Ozeki
- S Turro
- Sally Martin
- Samantha Murphy
- SC Frost
- SP Davies
- SW Eastman
- T Yamaguchi
- W Fei
- Y Guo
- Publication venue
- Public Library of Science
- Publication date
- 01/12/2010
- Field of study
Lipid droplets (LDs) are dynamic cytoplasmic organelles containing neutral lipids and bounded by a phospholipid monolayer. Previous studies have suggested that LDs can undergo constitutive homotypic fusion, a process linked to the inhibitory effects of fatty acids on glucose transporter trafficking. Using strict quantitative criteria for LD fusion together with refined light microscopic methods and real-time analysis, we now show that LDs in diverse cell types show low constitutive fusogenic activity under normal growth conditions. To investigate the possible modulation of LD fusion, we screened for agents that can trigger fusion. A number of pharmacological agents caused homotypic fusion of lipid droplets in a variety of cell types. This provided a novel cell system to study rapid regulated fusion between homotypic phospholipid monolayers. LD fusion involved an initial step in which the two adjacent membranes became continuous (<10 s), followed by the slower merging (100 s) of the neutral lipid cores to produce a single spherical LD. These fusion events were accompanied by changes to the LD surface organization. Measurements of LDs undergoing homotypic fusion showed that fused LDs maintained their initial volume, with a corresponding decrease in surface area suggesting rapid removal of membrane from the fused LD. This study provides estimates for the level of constitutive LD fusion in cells and questions the role of LD fusion in vivo. In addition, it highlights the extent of LD restructuring which occurs when homotypic LD fusion is triggered in a variety of cell types
Mesosphere/lower thermosphere prevailing wind model
- Author
- Aso T.
- Batista P.
- Clark R.
- Fahrutdinova A.
- Forbes J.
- Franke S.
- Fraser G.
- Fritts D.
- Gurubaran S.
- Hocking W.
- Hoffmann P.
- Igarashi K.
- Jacobi C.
- Korotyshkin D.
- Kovalam S.
- Kuerschner D.
- MacDougall J.
- Malinga S.
- Manson A.
- Meek C.
- Merzlyakov E.
- Mitchell N.
- Murayama Y.
- Murphy D.
- Nakamura T.
- Ortland D.
- Palo S.
- Pancheva D.
- Poole G.
- Portnyagin Y.
- Rajaram R.
- Riggin D.
- Singer W.
- Solovjova T.
- Taylor M.
- Thayaparan T.
- Tsuda T.
- Tsutsumi M.
- Vincent R.
- Publication venue
- Publication date
- 01/01/2004
- Field of study
The mesosphere/lower thermosphere (MLT) wind data from the 46 ground-based (GB) MF and meteor radar (MR) stations, located at the different latitudes over the globe, and the space-based (SB) HRDI data were used for constructing of the empirical global climatic 2-D prevailing wind model at 80-100 km heights for all months of the year. The main data set is obtained during 1990-2001 period. It is shown that the three datasets (MF, MR, HRDI) are mainly well correlated. However, a certain systematic bias between the GB and SB data at 96 km exists, as well as that between the MF and MR data higher 88 km. Simple correction factors are proposed to minimize these biases. The 2-D distant-weighted least-square interpolation procedure for some arbitrary collection of points was used for drawing model contour plots. The model is available in the computer readable form and may be used for construction of the new CIRA model. © 2004 COSPAR. Published by Elsevier Ltd. All rights reserved
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
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- A. -G. Wu
- A. C. Ma
- A. K. Au
- Abdel-Aziz A. K.
- Abdelfatah S.
- Abdellatif M.
- Abdoli A.
- Abel S.
- Abeliovich H.
- Abildgaard M. H.
- Abudu Y. P.
- Acevedo-Arozena A.
- Adamopoulos I. E.
- Adeli K.
- Adolph T. E.
- Adornetto A.
- Aflaki E.
- Agam G.
- Agarwal A.
- Aggarwal B. B.
- Agnello M.
- Agostinis P.
- Agrewala J. N.
- Agrotis A.
- Aguilar P. V.
- Ahmad S. T.
- Ahmed Z. M.
- Ahumada-Castro U.
- Aits S.
- Aizawa S.
- Akkoc Y.
- Akoumianaki T.
- Akpinar H. A.
- Al-Abd A. M.
- Al-Akra L.
- Al-Gharaibeh A.
- Alaoui-Jamali M. A.
- Alberti S.
- Alcocer-Gomez E.
- Alessandri C.
- Ali M.
- Alim Al-Bari M. A.
- Aliwaini S.
- Alizadeh J.
- Almacellas E.
- Almasan A.
- Alonso A.
- Alonso G. D.
- Altan-Bonnet N.
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- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
Lipid droplets: a classic organelle with new outfits
- Author
- A Garcia
- A Lass
- A Marcinkiewicz
- A Pol
- A Uittenbogaard
- AB Novikoff
- AG Ostermeyer
- AG Ostermeyer
- AK Agarwal
- AM Dvorak
- AM Dvorak
- AM Fra
- AS Greenberg
- B Magnusson
- B Razani
- BH Chang
- BH Stemberger
- BI Giasson
- BL Trigatti
- C Lefevre
- C Londos
- C Londos
- C Sztalryd
- C Sztalryd
- CA Kim
- CE Mountford
- D Binns
- D Corda
- D Debarre
- D Marchesan
- D Sorger
- D Zweytick
- DJ Lacey
- DJ McGookey
- DJ Murphy
- DJ Murphy
- DK Sharma
- DL Brasaemle
- DL Brasaemle
- DL Brasaemle
- E Umlauf
- EJ Blanchette-Mackie
- ES Tai
- FN Ghadially
- G Barba
- G Murphy Jr
- G Wanner
- G Wanner
- G Xu
- GF Gibbons
- GJ Praefcke
- GWC Kaye
- H Robenek
- H Robenek
- HC Wan
- HJ Manen van
- HL Ploegh
- HP Moore
- HT McMahon
- HW Heid
- J Magre
- JC Riemersma
- JE Schaffer
- Jinglei Cheng
- JL McManaman
- JL Webb
- JM Hakumaki
- JP Segrest
- JP Whitehead
- JT Tansey
- K Tauchi-Sato
- KF Buhman
- KM Szymanski
- KN Mahajan
- KS Carroll
- KT Dalen
- L Andersson
- L Kuerschner
- LL Listenberger
- LL Listenberger
- LL Luckenbill
- LS Ramsammy
- M Baba
- M Drab
- M Murata
- M Nagayama
- M Schrader
- M Waltermann
- M Waltermann
- MA Fernandez
- MA Welte
- MA Welte
- MA Welte
- Michitaka Suzuki
- MJ Robenek
- N Nakamura
- NA Ducharme
- NB Cole
- NE Wolins
- NE Wolins
- NE Wolins
- NE Wolins
- P Bostrom
- P Bostrom
- P Greenspan
- P Liu
- P Liu
- P Targett-Adams
- PM Gocze
- PT Bozza
- R Bartz
- R Bussell Jr
- R Leber
- R Lehner
- S Angermuller
- S Boulant
- S Cermelli
- S Fukumoto
- S Le Lay
- S Martin
- S Martin
- S Martin
- S Miura
- S Ozeki
- S Prattes
- S Sato
- S Turro
- SJ Hickenbottom
- SJ Smith
- SJ Stone
- ST Shi
- SY Cho
- T Fujimoto
- T Fujimoto
- T Hevonoja
- T Yamaguchi
- T Yamaguchi
- Toyoshi Fujimoto
- TY Chang
- V Puri
- V Subramanian
- W Fei
- W Yu
- WW Franke
- X Nan
- Y Fujimoto
- Y Kumar
- Y Miyanari
- Y Ohsaki
- Y Ohsaki
- Y Ohsaki
- Yuki Ohsaki
- Yuki Shinohara
- Publication venue
- Springer-Verlag
- Publication date
- 01/01/2008
- Field of study
Lipid droplets are depots of neutral lipids that exist virtually in any kind of cell. Recent studies have revealed that the lipid droplet is not a mere lipid blob, but a major contributor not only to lipid homeostasis but also to diverse cellular functions. Because of the unique structure as well as the functional importance in relation to obesity, steatosis, and other prevailing diseases, the lipid droplet is now reborn as a brand new organelle, attracting interests from researchers of many disciplines
Palynology of a terrestrial coal-bearing series across the Triassic/Jurassic boundary (Mecsek Mts, Hungary)
- Author
- Abbink O.A.
- Abbink O.A.
- Abbink O.A.
- Annette E. Götz
- Barbacka M.
- Barbacka M.
- Barbacka M.
- Bleahu M.
- BĂłna J.
- BĂłna J.
- BĂłna J.
- BĂłna J.
- BĂłna J.
- Cohen A.S.
- Cohen A.S.
- Grime J.P.
- Haas J.
- Haas J.
- Hornung J.
- JĂłzsef PĂĄlfy
- Katrin Ruckwied
- Kuerschner W. M.
- KĂĄli Z.
- Lund J.J.
- Lund J.J.
- McElwain J.C.
- McElwain J.C.
- Nagy E.
- NĂ©medi Varga Z.
- Olsen P.E.
- OrĆowska-ZwoliĆska T.
- Schulz E.
- Steffen D.
- Vakhrameev V.A.
- Voigt S.
- Weiss M.
- Ăkos Török
- Publication venue
- 'Akademiai Kiado Zrt.'
- Publication date
- Field of study
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
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- Abdel-Aziz AK
- Abdelfatah S
- Abdellatif M
- Abdoli A
- Abel S
- Abeliovich H
- Abildgaard MH
- Abudu YP
- Acevedo-Arozena A
- Adamopoulos IE
- Adeli K
- Adolph TE
- Adornetto A
- Aflaki E
- Agam G
- Agarwal A
- Aggarwal BB
- Agnello M
- Agostinis P
- Agrewala JN
- Agrotis A
- Aguilar PV
- Ahmad ST
- Ahmed ZM
- Ahumada-Castro U
- Aits S
- Aizawa S
- Akkoc Y
- Akoumianaki T
- Akpinar HA
- Al-Abd AM
- Al-Akra L
- Al-Gharaibeh A
- Alaoui-Jamali MA
- Alberti S
- Alcocer-GĂłmez E
- Alessandri C
- Ali M
- Alim Al-Bari MA
- Aliwaini S
- Alizadeh J
- Almacellas E
- Almasan A
- Alonso A
- Alonso GD
- Altan-Bonnet N
- Altieri DC
- Alves da Costa C
- Alves S
- Alzaharna MM
- Amadio M
- Amantini C
- Amaral C
- Ambrosio S
- Amer AO
- Ammanathan V
- An Z
- Andersen SU
- Andrabi SA
- Andrade-Silva M
- Andres AM
- Angelini S
- Ann D
- Anozie UC
- Ansari MY
- Antas P
- Antebi A
- AntĂłn Z
- Anwar T
- Apetoh L
- Apostolova N
- Araki T
- Araki Y
- Arasaki K
- Araya J
- AraĂșjo WL
- Arden C
- Arguelles S
- Arias E
- Arikkath J
- Arimoto H
- Ariosa AR
- Armstrong-James D
- Arnauné-Pelloquin L
- Aroca A
- Arroyo DS
- Arsov I
- Artero R
- Arévalo M-A
- Asaro DML
- Aschner M
- Ashrafizadeh M
- Ashur-Fabian O
- Atanasov AG
- Au AK
- Auberger P
- Auner HW
- Aurelian L
- Autelli R
- Avagliano L
- Aveic S
- Aveleira CA
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- Zorzano A
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- Ălvarez ĂMC
- Ăvalos Y
- Ănal G
- ĂstĂŒn S
- ÄoliÄ M
- ÄokiÄ J
- Ćœerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
DAG tales: the multiple faces of diacylglycerolâstereochemistry, metabolism, and signaling
- Author
- A Dietrich
- A Kornberg
- A Lass
- A Ligresti
- A Qiao
- A Roussel
- AC Lake
- AC Newton
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Adansonia digitata and Adansonia gregorii fruit shells serve as a protection against high temperatures experienced during wildfires
- Author
- A Patrut
- A Poljak
- AC Miranda
- C Cornu
- CE Nano
- CRY Munthali
- CS Duvall
- DA Baum
- DA Baum
- DE Kretschmann
- DMJS Bowman
- G Bauer
- GE Wickens
- GJ Esenowo
- GPP Kamatou
- J Gebauer
- J Owen
- J Razanameharizaka
- J Walker
- JA Rosell
- JG Pausas
- JH McDonald
- JL Schafer
- JMLP Tsy
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- M Gashaw
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- RT Wilson
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- SM Venter
- SR Turner
- T Vigilante
- TD Auld
- V Babrauskas
- W SchĂŒle
- W Stuppy
- WA Hoffmann
- WSW Trollope
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- Field of study