9 research outputs found
Chronic Nicotine Modifies Skeletal Muscle Na,K-ATPase Activity through Its Interaction with the Nicotinic Acetylcholine Receptor and Phospholemman
- Author
- A Gottschalk
- Alexander V. Chibalin
- Alexander V. Prokofiev
- Alexander V. Vasiliev
- AV Chibalin
- Boubacar Benziane
- DH Brunzell
- G Blanco
- H Garty
- H Wang
- I Krivoi
- I Romero-Calvo
- Igor I. Krivoi
- II Krivoi
- J Bossuyt
- J Orlowski
- J Reis
- JA Heiny
- JA Sparks
- JM Lindstrom
- Judith A. Heiny
- K Dey
- K Geering
- K Geering
- L Larsson
- L Wang
- MK Rasmussen
- Mohammed Akaaboune
- N Sperelakis
- NL Benowitz
- PE Leite
- PP Rowell
- R Kragenbrink
- RH Henning
- RL Ruff
- RL Ruff
- RW Mercer
- S Schiaffino
- SD Angelantonio
- VI Pidoplichko
- Violetta V. Kravtsova
- VV Kravtsova
- Publication venue
- Public Library of Science
- Publication date
- 19/03/2012
- Field of study
Our previous finding that the muscle nicotinic acetylcholine receptor (nAChR) and the Na,K-ATPase interact as a regulatory complex to modulate Na,K-ATPase activity suggested that chronic, circulating nicotine may alter this interaction, with long-term changes in the membrane potential. To test this hypothesis, we chronically exposed rats to nicotine delivered orally for 21–31 days. Chronic nicotine produced a steady membrane depolarization of ∼3 mV in the diaphragm muscle, which resulted from a net change in electrogenic transport by the Na,K-ATPase α2 and α1 isoforms. Electrogenic transport by the α2 isoform increased (+1.8 mV) while the activity of the α1 isoform decreased (−4.4 mV). Protein expression of Na,K-ATPase α1 or α2 isoforms and the nAChR did not change; however, the content of α2 subunit in the plasma membrane decreased by 25%, indicating that its stimulated electrogenic transport is due to an increase in specific activity. The physical association between the nAChR, the Na,K-ATPase α1 or α2 subunits, and the regulatory subunit of the Na,K-ATPase, phospholemman (PLM), measured by co-immuno precipitation, was stable and unchanged. Chronic nicotine treatment activated PKCα/β2 and PKCδ and was accompanied by parallel increases in PLM phosphorylation at Ser63 and Ser68. Collectively, these results demonstrate that nicotine at chronic doses, acting through the nAChR-Na,K-ATPase complex, is able to modulate Na,K-ATPase activity in an isoform-specific manner and that the regulatory range includes both stimulation and inhibition of enzyme activity. Cholinergic modulation of Na,K-ATPase activity is achieved, in part, through activation of PKC and phosphorylation of PLM
Multi-messenger observations of a binary neutron star merger
- Author
- Aab A
- Aartsen MG
- Abbott BP
- Abbott R
- Abbott TD
- Abbott TMC
- Abdalla H
- Abe F
- Abeysekara AU
- Abramo LR
- Abramowski A
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- Acernese F
- Acero F
- Ackermann M
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- Albuquerque IFM
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- Piro AL
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- Zadrozny A
- Zadrozny A
- Zaharijas G
- Zaltzman M
- Zanin R
- Zanolin M
- Zaremba M
- Zarnecki AF
- Zas E
- Zavrtanik D
- Zavrtanik M
- Zdziarski AA
- Zech A
- Zefi F
- Zelenova T
- Zendri J-P
- Zenko T
- Zenteno A
- Zepeda A
- Zertuche L Magaa
- Zevin M
- Zhang AM
- Zhang B-B
- Zhang C
- Zhang CL
- Zhang CM
- Zhang F
- Zhang H
- Zhang HM
- Zhang J
- Zhang L
- Zhang M
- Zhang Q
- Zhang S
- Zhang SN
- Zhang T
- Zhang T
- Zhang W
- Zhang WC
- Zhang WZ
- Zhang Y
- Zhang Y
- Zhang Y
- Zhang Y-H
- Zhang YF
- Zhang YJ
- Zhang Z
- Zhang ZL
- Zhao C
- Zhao HS
- Zhao JL
- Zhao W
- Zhao XF
- Zheng SJ
- Zhou H
- Zhou J
- Zhou M
- Zhou Z
- Zhu SJ
- Zhu XJ
- Zhu Y
- Zhu YX
- Zhu Z
- Ziegler A
- Zimmerman AB
- Zimmermann B
- Zimnukhov DS
- Ziolkowski M
- Zoll M
- Zong Z
- Zorn J
- Zornoza JD
- Zou CL
- Zuccarello F
- Zucker ME
- Zuniga J
- Zweizig J
- Zywucka N
- Publication venue
- 'American Astronomical Society'
- Publication date
- 01/01/2017
- Field of study
On 2017 August 17 a binary neutron star coalescence candidate (later designated GW170817) with merger time 12:41:04 UTC was observed through gravitational waves by the Advanced LIGO and Advanced Virgo detectors. The Fermi Gamma-ray Burst Monitor independently detected a gamma-ray burst (GRB 170817A) with a time delay of ~1.7 s with respect to the merger time. From the gravitational-wave signal, the source was initially localized to a sky region of 31 deg2 at a luminosity distance of 40+8-8 Mpc and with component masses consistent with neutron stars. The component masses were later measured to be in the range 0.86 to 2.26 Mo. An extensive observing campaign was launched across the electromagnetic spectrum leading to the discovery of a bright optical transient (SSS17a, now with the IAU identification of AT 2017gfo) in NGC 4993 (at ~40 Mpc) less than 11 hours after the merger by the One- Meter, Two Hemisphere (1M2H) team using the 1 m Swope Telescope. The optical transient was independently detected by multiple teams within an hour. Subsequent observations targeted the object and its environment. Early ultraviolet observations revealed a blue transient that faded within 48 hours. Optical and infrared observations showed a redward evolution over ~10 days. Following early non-detections, X-ray and radio emission were discovered at the transient’s position ~9 and ~16 days, respectively, after the merger. Both the X-ray and radio emission likely arise from a physical process that is distinct from the one that generates the UV/optical/near-infrared emission. No ultra-high-energy gamma-rays and no neutrino candidates consistent with the source were found in follow-up searches. These observations support the hypothesis that GW170817 was produced by the merger of two neutron stars in NGC4993 followed by a short gamma-ray burst (GRB 170817A) and a kilonova/macronova powered by the radioactive decay of r-process nuclei synthesized in the ejecta
Cancer Biomarker Discovery: The Entropic Hallmark
- Author
- A Alcaraz
- A Arabzadeh
- A Bagri
- A Balbin
- A Bantis
- A Ben-Naim
- A Bolander
- A Buhmeida
- A Burykin
- A Chetcuti
- A de Baey
- A Efeyan
- A Eroglu
- A Fabarius
- A Forget
- A Fujita
- A Geirsson
- A Geirsson
- A Geirsson
- A Guffanti
- A Hugel
- A Inoue
- A Isidoro
- A Jang
- A Kollara
- A Kuzmanov
- A Lundqvist
- A Maria McCrohan
- A Marreiros
- A Mendes
- A Mitra
- A Nassar
- A Petitjean
- A Petitjean
- A Pinzon-Charry
- A Richmond
- A Roesch
- A Santinelli
- A Schmidt
- A Shapiro
- A Sreekumar
- A Takeno
- A Urbanucci
- A Winter
- A Yemelyanov
- AA Babiker
- AA Babiker
- AA Tarhini
- AC Dudley
- AD Judge
- AD Ortega
- AG Puebla-Mora
- AH Fox
- AH Fox
- AI Riker
- AJ Liu
- AK Meeker
- AK Panigrahi
- AK Witkiewicz
- AL Cheung
- AL Fachin
- AL Gartel
- AL Okorokov
- AM Craig
- AM Lena
- AM Levin
- AM Tokes
- AP South
- AS Payne
- AS Verkman
- AS Verkman
- AS Verkman
- AS Wierzbicki
- AV Skamrov
- AW Maniccia
- B Cinar
- B Gao
- B Ouyang
- B Ren
- B Ryu
- B Tycko
- B Vukovic
- B Wu
- B Wu
- BD Dimitrov
- BF Gilmore
- BF Goncalves
- BF Skinnider
- BK Zehentner
- BL Adamsen
- BL de Groot
- BR Johnson
- BR Middleman
- BS Strauss
- C Adami
- C Bastide
- C Cao
- C Cybulski
- C Haqq
- C Hayashi
- C Hornig
- C Ivorra
- C Kumar-Sinha
- C Langner
- C Magi-Galluzzi
- C Magi-Galluzzi
- C Muller-Tidow
- C Nessler-Menardi
- C Nunez
- C Pequeux
- C Rajesh
- C Xu
- C Yuli
- CD Sturgis
- CD Truong
- CG Pham
- CG Rogers
- CG Rogers
- CJ Hutchison
- CJ Pronk
- CK Mavis
- CL Stewart
- CL Wu
- CM Caves
- CM Caves
- CM Clemson
- CM Perou
- CP Gray
- CP Gray
- CP Gray
- CR Mangahas
- CS Bond
- D Acehan
- D Bonn
- D Denhardt
- D Fu
- D Gilley
- D Gisselsson
- D Hanahan
- D Javelaud
- D Kroepfl
- D Lodygin
- D Maraldo
- D Ouazia
- D Scadden
- D Wang
- D Wang
- D Wang
- D Weckermann
- D Wodarz
- DA Shoskes
- DA Tennant
- DE Hansel
- DF Gleason
- DG Albertson
- DG Tenen
- DH Palmer
- DJ Darley
- DJ Grignon
- DJ Smit
- DJ Son
- DJ Wong
- DJC MacKay
- DK Koynova
- DK Lee
- DM Kube
- DM Peehl
- DR Wonsey
- DS Perez
- DV Makarov
- DV Makarov
- E Beitz
- E Beitz
- E Cabuy
- E Fagiani
- E Flannery
- E Geissinger
- E Kikuchi
- E Kruse
- E Sbisa
- E Sprecher
- E Tajkhorshid
- EA Ostrander
- EH Feng
- EH Feng
- EM Rosen
- EM Rosen
- EM Schaeffer
- EO Kehinde
- ET Canepa
- EV Vykhovanets
- EY Lin
- EY Tan
- F Bai
- F Bonetto
- F Boralevi
- F Buback
- F Colotta
- F Langer
- F Saad
- F Tas
- F Yang
- FS Krause
- G Benga
- G Bhanot
- G Blandino
- G Buchanan
- G Kaic
- G Kristiansen
- G Kristiansen
- G Kroemer
- G Murugaiyan
- G Petrovics
- G Pirtskhalaishvili
- G Russo
- G Sardana
- G Stirling
- G Tscheudschilsuren
- G Untergasser
- G Venkataraman
- G von Figura
- GA Jarvis
- GE Crooks
- GF Azzone
- GF Ding
- GL Shen-Ong
- GP Bienert
- GQ Daley
- GR Ribeiro
- GS Palapattu
- GV Glinsky
- GV Glinsky
- H Chang-zheng
- H Chen
- H Dzojic
- H Gronberg
- H Haghnegahdar
- H Harant
- H Harlin
- H Kida
- H Li
- H Liu
- H Miyake
- H Nemoto
- H Ostrer
- H Pilch
- H Rangaswami
- H Rangaswami
- H Rangaswami
- H Ren
- H Roca
- H Roca
- H Samaratunga
- H Savli
- H Schlechte
- H Schoder
- H Sheng
- H Sunwoo
- H Then
- H Wang
- H Wang
- HC Lee
- HG Thomas
- HJ Worman
- HL Winfield
- HS Leff
- HT Quan
- HY Vu
- HZ Zhang
- I Agalliu
- I Bae
- I Ben-Porath
- I Grosse
- I Haritoglou
- I Leav
- I Marinescu
- I Moll
- I Sakai
- IE Wertz
- IK Lim
- IL Tourkova
- IM Bachmann
- IM Shih
- IW Reiniger
- IY Dodin
- J Bartkova
- J Edwards
- J Fellenberg
- J Gille
- J Graells
- J Jaeger
- J Johnson
- J Lammerding
- J Laoukili
- J Lapointe
- J Linden
- J Luo
- J Luo
- J Luo
- J Mandelin
- J Melamed
- J Moser
- J Rangel
- J Rapley
- J Reimand
- J Ruiz-Ederra
- J Schmitz
- J Schultz
- J Soikkeli
- J Stewart
- J Suh
- J Walter-Yohrling
- J Wang
- J Wang
- J Weiske
- J Xu
- J Yang
- J Yang
- J Zheng
- JA Camargo
- JA Douglas
- JA Hackett
- JA Karam
- JA McGrath
- JA McGrath
- JA McGrath
- JA McGrath
- JA Mobley
- JA Pettus
- JB Roche
- JC Cheville
- JD French
- JD Licchesi
- JD Owen
- JE Lai-Cheong
- JE Sleeman
- JE Wilusz
- JG Wen
- JH Lee
- JH Luo
- JJ Brey
- JJ Park
- JJ Raffoul
- JJ Tseng
- JJ Van den Oord
- JK Wahl 3rd
- JL Broers
- JL Herrmann
- JL Phillips
- JM Brandner
- JM Bridger
- JM Cummins
- JM Gonzalez
- JM Lizcano
- JM Muller
- JM Muller
- JM Parrondo
- JM Saffin
- JN Hutchinson
- JN Mubiru
- JN Mubiru
- JN Mubiru
- JP Arbitrario
- JP Clark
- JP Ehlers
- JP Fruehauf
- JP Struewing
- JR Cansino Alcaide
- JR McMillan
- JS Butler
- JS Butler
- JS Fang
- JS Hub
- JS Lee
- JS Mattick
- JS Mattick
- JS Mattick
- JT Bishoff
- JT Chang
- JW Denham
- K Armstrong
- K Fujita
- K Ishibashi
- K Ishitani
- K Kami
- K Kasuno
- K Kumagai
- K Mizutani
- K Namiki
- K Ruan
- K Ruan
- K Shilo
- K Sircar
- K Suzuki
- K Swisshelm
- K Takahara
- K Tani
- K Tokunaga
- K Tomkova
- K Trpkov
- K Yamada
- KA Tasken
- KA Zuhlke
- KH Hoffmann
- KH Tsui
- KL Nastiuk
- KL Simpson
- KL van Golen
- KN Ekdahl
- KP Porkka
- KR Ghani
- KV Prasanth
- L Capparuccia
- L Carlsson
- L Cheng
- L de Meis
- L Galluzzi
- L Kneisel
- L Lessard
- L Li
- L Moro
- L Moro
- L O'Regan
- L Packer
- L Pasini
- L True
- L Verdoucq
- L Verschooten
- L Xu
- L Zheng
- LA Diaz-Martinez
- LB Mora
- LE Clarke
- LE Finlan
- LF Brown
- LF Zerbini
- LL Chen
- LL Smith
- LL Smith
- LM Godsel
- LP Kunju
- M Aalamian-Matheis
- M Aghaei
- M Bakhanashvili
- M Boury-Jamot
- M Boury-Jamot
- M Buxade
- M Chellaiah
- M Cimitan
- M Craig
- M Dumas
- M Dundr
- M Esteller
- M Estler
- M Fabbri
- M Fukunaga-Kalabis
- M Fukunaga-Kalabis
- M Furuno
- M Gilbert
- M Hara-Chikuma
- M Hara-Chikuma
- M Hara-Chikuma
- M Hara-Chikuma
- M Hatzfeld
- M Hatzfeld
- M Heenen
- M Ismail
- M Karaivanov
- M Kashani-Sabet
- M Kato
- M Katoh
- M Kinoshita
- M Korabiowska
- M Kulesz-Martin
- M Lei
- M Lisovsky
- M Marko
- M Mellado
- M Mishima
- M Mockenhaupt
- M Moghaddami
- M Moghaddami
- M Nessling
- M Olsson
- M Onaitis
- M Parisi
- M Schostak
- M Tischkowitz
- M Traka
- M Tribus
- M Varma
- M Venoux
- M Watanabe
- M Yang
- M Yasui
- M Zhou
- M Zhou
- M Zhou
- MA Castro
- MA Chekmareva
- MA Chellaiah
- MA Ficazzola
- MA Halsey
- MA Roder
- MA Rubin
- MA Rubin
- MA Rubin
- MB Martens
- MB Rettig
- MC Caino
- MC Schumacher
- MD Desrosiers
- MD Duff
- MD Lloyd
- ME Blank
- ME Grossmann
- ME Grossmann
- ME Laski
- ME Morrison
- MF Fraga
- MH Vaarala
- MK Thomsen
- MK Thomsen
- MM Petrovic
- MM Rashid
- MR Rosner
- MS O'Connor
- MS Tretiakova
- MT Kalcioglu
- MT Ling
- MT Martin
- MT Sung
- MV Blagosklonny
- MY Lee
- N Bahamontes-Rosa
- N Donin
- N Konishi
- N Lapteva
- N Maeda
- N Nadiminty
- N Rabiau
- N Singh
- NG Hussein
- NI Andreyev
- NJ Fisch
- NV Whittock
- NV Whittock
- O Bettendorf
- O Canbolat
- O Itzhaki
- O Kwon
- OA Rosso
- OW Rokhlin
- P Agre
- P Agre
- P Agre
- P Agre
- P Allavena
- P Berthon
- P Boukamp
- P Cossu-Rocca
- P Dhawan
- P Dhawan
- P Duesberg
- P Duesberg
- P Duesberg
- P Hainaut
- P Ji
- P Karakiewicz
- P Koivisto
- P Roy-Burman
- P Rustin
- P Sini
- P Slijepcevic
- P Sotomayor
- P Sotomayor
- P Steigemann
- P Zhang
- Pablo Moscato
- PD Walden
- PG Gallagher
- PH Gumerlock
- PH Konig
- PI Nedvetsky
- PJ Gray Jr
- PJ Zielie
- PL Chang
- PM Lacal
- PM Lacal
- PM Mordaka
- PM Steijlen
- PT Landsberg
- PT Went
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- R Agarwal
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- R Das
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- R Klimek
- R Klimek
- R Kuefer
- R Lin
- R Mazzucchelli
- R Mukherjee
- R Radosavljevic
- R Rai
- R Sougrat
- RA Craven
- RA Hegele
- RA Sturm
- RA Weinberg
- RC Lee
- RD Ballal
- RD Loberg
- RD Loberg
- RD Loberg
- RD Loberg
- Regina Berretta
- RG Uzzo
- RJ Jin
- RJ Urban
- RJ Webster
- RL Boguslavsky
- RL Shattuck
- RMH Lopez-Ruiz
- RP Ciavarra
- RP Ciavarra
- RP Singh
- RS Weinstein
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- RW DeVere White
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- S Brychtova
- S Cardinale
- S Das
- S Das
- S Dettwiler
- S Di Cesare
- S Doratiotto
- S Ersoy-Evans
- S Fan
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- S Ghosh
- S Gunia
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- S Hauptmann
- S Hiratsuka
- S Horsburgh
- S Huerta-Yepez
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- S Jhavar
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- S Kyle
- S Landreville
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- S Morohashi
- S Olgac
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- S Philip
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- S Rankin
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- SJ Yeung
- SK Kang
- SL Kong
- SL Zheng
- SM Edwards
- SM Ho
- SM Saparov
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- SR Alonso
- SS Kadkol
- SV Setzer
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- T Drewa
- T Hoevel
- T Ishiyama
- T Jamaspishvili
- T Kusumi
- T Litman
- T Ma
- T Mirtti
- T Murakami
- T Oyama
- T Schlomm
- T Schlomm
- T Sheridan
- T Shimizu
- T Sobolik-Delmaire
- T Sun
- T Takahashi
- T Takeda
- T Thornburg
- T Watanabe
- T Yu
- TB Lewis
- TD Prickett
- TH Ecke
- TJ McDonnell
- TJ Park
- TL Schmit
- TL Schmit
- TO Nielsen
- TR Mercer
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- U Graeven
- U Gruneberg
- UV Wesley
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- V Barak
- V Fradet
- V Molinie
- V Molinie
- V Molinie
- V Molinie
- V Molinie
- V Molinie
- V Pekovic
- V Rajaram
- V Samanna
- V Wessagowit
- V Winnepenninckx
- VD Acevedo
- VK Vanguri
- VL Verstraeten
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- W Cosme-Blanco
- W Gade
- W Ritchie
- W Spirkl
- W Tettelbach
- W Wang
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- W Weichert
- W Weichert
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- WD Dunsmuir
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- William C. S. Cho
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- WK Lee
- X Chen
- X Cheng
- X Dong
- X Dong
- X Huang
- X Li
- X Liu
- X Liu
- X Meng
- X Ouyang
- X Tang
- X Wu
- X Zhang
- XJ Yang
- XQ Wang
- Y Bu
- Y Cai
- Y Deng
- Y Ito
- Y Katagiri
- Y Kozuka
- Y Lai
- Y Liu
- Y Lu
- Y Lu
- Y Ohyama
- Y Shav-Tal
- Y Sugiyama
- Y Sun
- Y Wang
- Y Wang
- Y Wu
- Y Yamamoto
- Y Yang
- Y Zhou
- YB Lim
- YC Chao
- YJ Ko
- YL Liu
- YN Liu
- YT Sasaki
- YT Sasaki
- YU Katagiri
- Z Jiang
- Z Jiang
- Z Jiang
- Z Jiang
- Z Jiang
- Z Rudzki
- ZA Dotan
- ZR Yurkovetsky
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2010
- Field of study
Background: It is a commonly accepted belief that cancer cells modify their transcriptional state during the progression of the disease. We propose that the progression of cancer cells towards malignant phenotypes can be efficiently tracked using high-throughput technologies that follow the gradual changes observed in the gene expression profiles by employing Shannon's mathematical theory of communication. Methods based on Information Theory can then quantify the divergence of cancer cells' transcriptional profiles from those of normally appearing cells of the originating tissues. The relevance of the proposed methods can be evaluated using microarray datasets available in the public domain but the method is in principle applicable to other high-throughput methods. Methodology/Principal Findings: Using melanoma and prostate cancer datasets we illustrate how it is possible to employ Shannon Entropy and the Jensen-Shannon divergence to trace the transcriptional changes progression of the disease. We establish how the variations of these two measures correlate with established biomarkers of cancer progression. The Information Theory measures allow us to identify novel biomarkers for both progressive and relatively more sudden transcriptional changes leading to malignant phenotypes. At the same time, the methodology was able to validate a large number of genes and processes that seem to be implicated in the progression of melanoma and prostate cancer. Conclusions/Significance: We thus present a quantitative guiding rule, a new unifying hallmark of cancer: the cancer cell's transcriptome changes lead to measurable observed transitions of Normalized Shannon Entropy values (as measured by high-throughput technologies). At the same time, tumor cells increment their divergence from the normal tissue profile increasing their disorder via creation of states that we might not directly measure. This unifying hallmark allows, via the the Jensen-Shannon divergence, to identify the arrow of time of the processes from the gene expression profiles, and helps to map the phenotypical and molecular hallmarks of specific cancer subtypes. The deep mathematical basis of the approach allows us to suggest that this principle is, hopefully, of general applicability for other diseases
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
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- Abdel-Aziz AK
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- Abdellatif M
- Abdoli A
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- 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-Gómez 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
- Antón Z
- Anwar T
- Apetoh L
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- Araki T
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- Arguelles S
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- Žerovnik 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
Functional consequences of subunit interactions in Na,K- and H,K-ATPases.
- Author
- A Ivanov
- A Shainskaya
- A Shainskaya
- AG Thérien
- AT Beggab
- B Attali
- B Forbush III
- B Küster
- BW Morrison
- C Toyoshima
- E Arystarkhova
- E Feraille
- E Or
- F Jaisser
- G Blanco
- G Crambert
- H Shi
- HK Simmerman
- HX Pu
- IC Meij
- JB Koenderink
- JR Moorman
- K Geering
- K Geering
- KA Eakle
- KJ Sweadner
- MA Lemmon
- P Béguin
- P Béguin
- P Béguin
- P Béguin
- P Jaunin
- RK Wetzel
- RW Mercer
- S Lutsenko
- S Lutsenko
- TE Colonna
- U Hasler
- U Hasler
- U Hasler
- WJ Rice
- X Fu
- Publication venue
- Publication date
- 01/01/2002
- Field of study
Subunit Composition and Role of Na+,K+-ATPases in Ventricular Myocytes
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- Arnon A Hamlyn JM, Blaustein MP.
- Blanco G Mercer RW.
- De Mello WC.
- Dostanic I Paul RJ, Lorenz JN, The
- Duffy HS Ashton AW, O&rsquo
- GOLOVINA V A
- Inoue M Imanaga I.
- Lin H Ozaki S, Fujishiro N, Takeda
- McDonough AA Zhang Y, Shin V, Fran
- Petrecca K Atanasiu R, Grinstein S
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- Schwinger RHG Wang J, Frank K, Mul
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- Wang J Schwinger RHG, Frank K, M
- Weingart R.
- WETZEL R K
- Wilson PD Devuyst O, Li X, Gatti L
- Zahler R Sun W, Ardito T, Zhang Z-
- Publication venue
- 'Physiological Society of Japan'
- Publication date
- 01/01/2006
- Field of study
Elevated Na+/K+-ATPase responses and its potential role in triggering ion reabsorption in kidneys for homeostasis of marine euryhaline milkfish (Chanos chanos) when acclimated to hypotonic fresh water
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- A Doulgerakia
- A Heijden
- AA McDonough
- B Sardella
- C Nebel
- C Schonrock
- CA Freire
- CH Fiske
- CH Lin
- CH Tang
- CH Tang
- CH Tang
- Cheng-Hao Tang
- CK Kang
- CK Tipsmark
- CK Tipsmark
- CK Tipsmark
- CK Tipsmark
- CP Cutler
- CP Hickman
- D Crear
- DH Evans
- DM Fambrough
- EE Deane
- F Katoh
- F Katoh
- FH Epstein
- FH Epstein
- FJ Arjona
- G Blanco
- G Venturini
- H Chasiotis
- H Miyazaki
- H Nishimura
- H Nishimura
- HH Taussky
- J Hiroi
- JL Gallis
- JL Renfro
- JW Semple
- K Takeyasu
- KA Sloman
- KJ Livak
- KW Beyenbach
- LS Krayushkina
- M Endo
- M Herrera
- M Ogawa
- M Seidelin
- M Seidelin
- MKS Wong
- MS Marshall
- P Lasserre
- PP Hwang
- PP Hwang
- RL Post
- RP Ferraris
- RW Mercer
- RW Mercer
- S Madsen
- S Romao
- S Sangiao-Alvarellos
- SD McCormick
- SE Wendelaar Bonga
- SEW Bonga
- SF Perry
- SH Feng
- Shu-Chuan Tsai
- SP Kelly
- SP Kelly
- SXJ Cheng
- T Bagrinao
- Tatsuki Yoshinaga
- TO Nilsen
- Tsung-Han Lee
- Wen-Yi Wu
- WKF Tse
- WKF Tse
- WS Marshall
- YM Lin
- YM Lin
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Proteomic characterization of epicardial-myocardial signaling reveals novel regulatory networks including a role for NF-κB in epicardial EMT
- Author
- A Darehzereshki
- A Germani
- A Ruiz-Villalba
- A von Gise
- AA Beg
- AD Person
- AF Austin
- Alexander Urban
- AM Mellgren
- B Dawn
- B Kraut
- B Zhou
- BJ Martinsen
- C Gittenberger-de Groot a
- C Niehrs
- CJ Morabito
- CL Cortesio
- CL Smith
- CR Clark
- CR Hill
- D Dokic
- Devin Midura
- DGM Molin
- DM DeLaughter
- DW Huang
- E a Craig
- Federica Limana
- G Ryzhakov
- G van den Berg
- H Wu
- Hans-Georg Simon
- HE Olivey
- Hernandez-Gutierrez
- HM Shin
- I Stuckmann
- IM Verma
- J Wang
- JIE Hoffman
- JM Pérez-Pomares
- JR Burke
- JR Cooley
- K Wei
- KJ Lavine
- KJ Lavine
- LP Sanford
- M Chevallet
- M Greutmann
- M Ieda
- M Krainock
- M Maleszewska
- M Masters
- M Vega-Hernández
- M Wu
- MA Blanco
- MS Hayden
- MW Kelley
- N a M Bax
- N Bin-Nun
- N Smart
- NAM Bax
- NMS Van Den Akker
- NS Sánchez
- P Li
- P Sarkar
- Q Li
- Q. Tian Wang
- RE Welikson
- RJ Garriock
- RS Muraoka
- RS Ross
- RW Dettman
- S Ghosh
- S Govind
- S Hikoso
- SE Calvano
- SE Mercer
- SH Pae
- SJ Franco
- T Brade
- T Hiruma
- TN Petersen
- W Nickel
- WC Sha
- Y Ishii
- Y Kanegae
- Y Ma
- Yanyang Li
- Publication venue
- 'Public Library of Science (PLoS)'
- Publication date
- Field of study
Modulation of immune responses by targeting CD169/Siglec-1 with the glycan ligand
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- Abaddi A
- Abdulkhalek S
- Abe H
- Acosta-Blanco I
- Adamczyk B
- Adams P
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- Aderem A
- Adlercreutz D
- Aggeler R
- Agnew B
- Agravat S
- Akama TO
- Akita K
- Akutsu M
- Akçay G
- Albers SV
- Albiez RS
- Ali MF
- Allingham J
- Almeida I
- Alter G
- Amano J
- Amith SR
- Anastassiades T
- Andre S
- André S
- Angata K
- Angata K
- Angata K
- Aoki K
- Aoki K
- Apte A
- Arciniega-Fuentes MT
- Ardá A
- Aronica M
- Arteaga-Cabello FJ
- Aryal R
- Asada H
- Asakawa K
- Ashley J
- Ashmus R
- Assis R
- Aumiller JJ
- Azadi P
- Azadi P
- Azadi P
- Badish L
- Baggenstoss BA
- Baggenstoss BA
- Bahrke S
- Baksi K
- Bale MS
- Balland A
- Bally M
- Balsbaugh J
- Balsbaugh J
- Balzarini J
- Banerjee A
- Banerjee D
- Bao X
- Bao X
- Bao X
- Barb A
- Bartel F
- Batista F
- Baumeister H
- Beeton C
- Begonja AJ
- Betenbaugh M
- Beverley SM
- Bharadwaj R
- Bielik AM
- Bionda N
- Black I
- Blader I
- Bleuler-Martinez S
- Boccuto L
- Bochner B
- Boeggeman E
- Bond M
- Boons GJ
- Boons GJ
- Boons GJ
- Boons GJ
- Boons GJ
- Borisova S
- Borén T
- Boufala S
- Bovin NV
- Bovin NV
- Brade H
- Brade H
- Brade L
- Brade L
- Brady L
- Brewer C
- Briscoe A
- Brockhausen I
- Brockhausen I
- Brockhausen I
- Brockhausen I
- Brooks CL
- Brown K
- Brown RK
- Brown RK
- Brummet M
- Bullen J
- Bunt SK
- Burr T
- Cafarella T
- Calabretta P
- Calabro A
- Calle L
- Campbell H
- Canis K
- Cardenas G
- Carrington SD
- Caster C
- Castro E
- Catarello J
- Chachadi VB
- Chacko BK
- Chai W
- Chai W
- Chanda S
- Chandrasekaran A
- Chandy KG
- Chapman AB
- Chapman J
- Chaubard JL
- Chaubey A
- Chavaroche A
- Chen C
- Chen C
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- Chen HL
- Chen L
- Chen M
- Chen S
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- Chen W
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- Cheng PW
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- Cholleti S
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- d'Alarcao M
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- Zumwalt A
- Publication venue
- 'Oxford University Press (OUP)'
- Publication date
- 01/01/2011
- Field of study
A fundamental role in the plant-bacterium interaction for
Gram-negative phytopathogenic bacteria is played by membrane
constituents, such as proteins, lipopoly- or lipooligosaccharides
(LPS, LOS) and Capsule Polysaccharides (CPS).
In the frame of the understanding the molecular basis of plant bacterium interaction, the Gram-negative bacterium Agrobacterium vitis was selected in this study. It is a phytopathogenic member of the Rhizobiaceae family and it induces the crown gall disease selectively on grapevines (Vitis vinifera).
A. vitis wild type strain F2/5, and its mutant in the quorum
sensing gene ΔaviR, were studied. The wild type produces biosurfactants; it is considered a model to study surface motility, and it causes necrosis on grapevine roots and HR (Hypersensitive
Response) on tobacco. Conversely, the mutant does not show any
surface motility and does not produce any surfactant material;
additionally, it induces neither necrosis on grape, nor HR on
tobacco. Therefore, the two strains were analyzed to shed some
light on the QS regulation of LOS structure and the consequent
variation, if any, on HR response. LOS from both strains were isolated and characterized: the two LOS structures maintained several common features and differed for few others.
With regards to the common patterns, firstly: the Lipid A region
was not phosphorylated at C4 of the non reducing glucosamine
but glycosylated by an uronic acid (GalA) unit, secondly: a third
Kdo and the rare Dha (3-deoxy-lyxo-2-heptulosaric acid) moiety
was present.
Importantly, the third Kdo and the Dha residues were substituted
by rhamnose in a not stoichiometric fashion, giving four different
oligosaccharide species.
The proportions among these four species, is the key difference
between the LOSs from both the two bacteria.
LOS from both strains and Lipid A from wild type A. vitis are
now examined for their HR potential in tobacco leaves and grapevine roots