MiPschool Tromso-Bergen 2018
Tromso-Bergen, NO. 2018 Oct 20-24, 11th MitoEAGLE Training School - MiPschool 2018. From basics of mitochondrial physiology to cardiovascular health and disease. |
» Mitochondrial Physiology Society
Mitochondrial Physiology Society (2018-10-20) MitoGlobal
Abstract: MiPschool, Tromso-Bergen, Norway 2018
Venue and accommodation
- Hurtigruten
- Bergen to Tromso
- Norway
- Impressions: Ship and Hurtigruten travel offers
Local organizer
- Larsen Terje
- Faculty of Health Sciences, University of Tromsø
Lecturers
Harper Mary-Ellen (University of Ottawa, CA)
Hoppel Charles L (Case Western Reserve University, Cleveland, US)
Vendelin Marco (Tallin University of Technology, EE)
Gnaiger Erich (Medical University of Innsbruck, AT; Oroboros Instruments, AT)
Meet the expert
- Iglesias-GonzalezJ.JPG
Iglesias-Gonzalez Javier (Oroboros Instruments, Innsbruck, AT)
Larsen Terje (University of Tromsø, NO)
Makrecka-Kuka Marina (Latvian Institute of Organic Synthesis, LV)
Murray Andrew J (University of Cambridge, UK)
Schlattner Uwe (Université Grenoble Alpes, FR)
Wiesner Rudolf (Universtiy of Cologne, DE)
Wuest Rob (Academic Medical Center, NL)
Programme
Programme structure
- Check-in will take place on Saturday, October 20 from 21:00-23:30 pm at Skarven Bar downtown Tromsø, and on the Coastal Express on Sunday from 00:15-01:30 am.
- We will disembark on Wednesday, October 24 at 14:30 in Bergen.
- The voyage from Tromsø to Bergen
- Check-in will take place on Saturday, October 20 from 21:00-23:30 pm at Skarven Bar downtown Tromsø, and on the Coastal Express on Sunday from 00:15-01:30 am.
- The scientific sessions consist of introductory lectures, selected abstract presentations, and discussions in small groups in an open “meet the expert” format.
- Sessions E1 - E3: Meet the expert - open MitoEAGLE topics - MitoEAGLE Early Career Investigator Forum
- Session E4 – Open programme lectures: Programme decisions made during and by the MitoEAGLE/MiPschool (voted from the MitoEAGLE Early Career Investigator Forum)
- The scientific sessions consist of introductory lectures, selected abstract presentations, and discussions in small groups in an open “meet the expert” format.
- To all participants: Study and join as one of >425 co-authors
- MitoEAGLE preprint on Mitochondrial respiratory states and rates (Last update 2018-10-17, Version 44) - »Bioblast link«
- You will receive a hardcopy of Version 44 (40 pp.). You are invited to join as a co-author during the MitoEAGLE/MiPschool.
- To all participants: Study and join as one of >425 co-authors
Sessions with abstracts for oral presentations
» Final programme for download
A1. Mitochondrial physiology: pathways and coupling | Session | |
---|---|---|
Gnaiger 2018 MiPschool Tromso A1 | Mitochondrial states and rates: 1. Electron transfer pathways and respiratory control. 2. Coupling control. | Oral A1 |
B1. Energy transfer and movement of molecules in cardiomyocytes | Session | |
---|---|---|
Schlattner 2018 MiPschool Tromso B1 | Mitochondrial kinases: key players in respiratory control and energy transfer. | B1 Oral |
Vendelin 2018 MiPschool Tromso B1 | Restrictions to intracellular diffusion of ATP and ADP in cardiomyocytes. | B1 Oral |
Sunday, October 21 – Afternoon
C1. Selected abstracts: Cardiac OXPHOS | Session | |
---|---|---|
Pereira 2018 MiPschool Tromso C1 | Obesity-induced mitochondrial hepatic changes during pregnancy. | Oral C1 |
Goncalo Teixeira 2018 MiPschool Tromso C1 | Subchronic in vivo study for the evaluation of hepatic mitochondrial toxicity induced by silver nanoparticles. | Oral C1 |
Ma 2018 MiPschool Tromso C1 | Cardiolipin synthesis in brown and beige fat mitochondria is essential for systemic energy homeostasis. | C1 Oral |
C2. Selected abstracts: Cardioprotection | Session | |
---|---|---|
Kampa 2018 MiPschool Tromso C2 | Cardioprotective flavoniods as a natural modulators of mitoBKCa channel. | C2 Oral |
MartinsJD 2018 MiPschool Tromso C2 | Sweetheart: Cardiac consequences of fetal exposure to maternal gestational diabetes on the offspring mitochondrial function. | C2 Oral |
Tuncay 2018 MiPschool Tromso C2 | MitoTEMPO ameliorates hyperglycemia induced mitochondrial damage in cardiomyocytes. | C2 Oral |
Jansen 2018 MiPschool Tromso C2 | Dietary and pharmacological treatment of diet-induced obese mice – impact on mitochondrial function. | C2 Oral |
D1. Cardiovascular disease and mitochondrial medicine | Session | |
---|---|---|
Harper 2018 MiPschool Tromso D1 | OXPHOS efficiency in skeletal and cardiac muscles: Proton leaks, ROS and glutathione redox. | D1 Oral |
Hoppel 2018 MiPschool Tromso D1 | Two populations of muscle mitochondria: heart and skeletal muscle. | D1 Oral |
E1. MitoEAGLE Early Career Investigator Forum | Session | |
---|---|---|
Wiesner 2018 MiPschool Tromso E1 | Aging-related accumulation of mitochondrial DNA deletions in skeletal muscle occurs preferentially in Type IIb fibers – high mitophagic flux protects Type I fibers. | E1 |
Harper 2018 MiPschool Tromso E1 | Deacetylation acceleration of BAT thermogenesis. | E1 |
Iglesias-Gonzalez 2018 MiPschool Tromso E1 | Oscillations in mitochondrial ROS production during the early cell cycles in Xenopus embryos. | E1 |
Makrecka-Kuka 2018 MiPschool Tromso E1 | Cardiac fatty acid oxidation: from in vitro to in vivo. | E1 |
Murray 2018 MiPschool Tromso E1 | OXPHOS protocols: understanding the patterns. | E1 |
Vendelin 2018 MiPschool Tromso E1 | Introducing a platform for primary kinetics data analysis. | E1 |
E2. MitoEAGLE Early Career Investigator Forum - table discussions | Session | |
---|---|---|
Siewiera 2018 MiPschool Tromso E2 | Effect of metformin treatment on blood platelet bioenergetics and platelet function in STZ-diabetic and non-diabetic rats. | E2 |
Alves 2018 MiPschool Tromso E2 | Role for mitochondria on the response of highly proliferative and invasive bladder cancer cells to the combined inhibition of mTOR and SIRT1. | E2 |
Krajcova 2018 MiPschool Tromso E2 | High-resolution respirometry to assess function of mitochondria in native homogenates of human heart muscle. | E2 |
MartinsAD 2018 MiPschool Tromso E2 | Mitochondrial dynamics of human Sertoli cells under the effect of leptin and ghrelin. | E2 |
Huete-Ortega 2018 MiPschool Tromso E2 | High-resolution respirometry: new perspectives for the study of bioenergetics in algae and plants. | E2 |
Garipi 2018 MiPschool Tromso E2 | Phenotyping mitochondrial metabolism in Barrett’s metaplasia-dysplasia-adenocarcinoma sequence: respiratory capacity, extracelular proton flux and ROS production | E2 |
Puurand 2018 MiPschool Tromso E2 | Intracellular energy-transfer networks in health and disease – the results of oxygraphic studies. | E2 |
Cardoso 2018 MiPschool Tromso E2 | Concomitant respiration and ATP production measurements to analyse P»/O2 ratios at physiological normoxia. | E2 |
Kidere 2018 MiPschool Tromso E2 | Cytoplasmic hybrid cells as a model to characterize the OXPHOS system: control sample with glutamate metabolism defect. | E2 |
Storder 2018 MiPschool Tromso E2 | Investigaton on the role of the mitochondiral deacetylase Sirtuin 3 in adipose tissue. | E2 |
Fischer 2018 MiPschool Tromso E2 | Analysis of mitochondrial function in iron deficiency anemia and iron overload conditions. | E2 |
Li Puma 2018 MiPschool Tromso E2 | Fads2 exacerbates myocardial ischemia-reperfusion injury in mice: role of mitochondria. | E2 |
Monday, October 22 - Afternoon
A2. Mitochondrial physiology: protonmotive force | Session | |
---|---|---|
Gnaiger 2018 MiPschool Tromso A2 | The protonmotive force and respiratory control. 1. Coupling of electron transfer reactions to vectorial translocation of protons. 2. From Einstein’s diffusion equation on gradients to Fick’s law on compartments. | Oral A2 |
C3. Selected abstracts: Adipose and liver mitochondria | Session | |
---|---|---|
Torp 2018 MiPschool Tromso C3 | Intracellular complement factor 3 in the heart – a link to metabolism? | Oral C3 |
Isola 2018 MiPschool Tromso C3 | AMPK deficiency elicits changes in OXPHOS in heart mitochondria. | Oral C3 |
D2. Cardiac mitochondrial physiology and pathology | Session | |
---|---|---|
Vendelin 2018 MiPschool Tromso D2 | Modeling actomyosin contraction in the heart muscle. | D2 Oral |
Hoppel 2018 MiPschool Tromso D2 | Mitochondrial function during ischemia/reperfusion injury. | D2 Oral |
- E3: MitoEAGLE Early Career Investigator Forum E2: Meet the expert
Tuesday, October 23 – Afternoon
- E4: Open programme lectures: Programme decisions made during and by the MitoEAGLE/MiPschool
C4. Selected abstracts: Mitochondrial disorders, remodeling, and degenerative diseases | Session | |
---|---|---|
Vujacic-Mirski 2018 MiPschool Tromso C4 | Development of analytical assays for the detection and quantification of reactive oxygen and nitrogen species in an animal model of type 1 diabetes - ROS formation involving mitochondrial and NADPH oxidase. | C4 Oral |
Musiol 2018 MiPschool Tromso C4 | Alpha-tomatine as a novel membrane-permeabilizing agent for mitochondrial respiration measurements. | C4 Oral |
Bastos Sant'Anna Silva 2018 MiPschool Tromso C4 | Role of succinate in prostate cancer cells: uptake and mitochondrial respiratory function. | C4 Oral |
Vella 2018 MiPschool Tromso C4 | Exome analysis sheds light on mitochondrial disorders. | C4 Oral |
Crisostomo 2018 MiPschool Tromso C4 | Mitochondrion at the crosstalk between metabolic disease and dysfunction in male fertility? | C4 Oral |
Zdrazilova 2018 MiPschool Tromso C4 | Bioenergetic characterization of skin fibroblasts from patients with congenital disorders of glycosylation. | C4 Oral |
Wednesday, October 24 - Morning
D3. Mitochondrial function and cardioprotection | Session | |
---|---|---|
Wuest 2018 MiPschool Tromso D3 | Metabolic flexibility and mitochondrial function in the diabetic heart. | D3 Oral |
Boardman 2018 MiPschool Tromso D3 | High fat-load induces cardioprotection in hearts from obese mice. | Oral D3 |
Registration and further information
- The maximum number of attendees for the MiP/MitoEAGLE Training School 2018 of 65 participants is reached.
- closed
- MitoEAGLE
- The MitoEAGLE network aims to improve our knowledge on mitochondrial function in health and disease related to Evolution, Age, Gender, Lifestyle and Environment. Every study of mitochondrial (mt) function and disease is faced with EAGLE as the essential background conditions characterizing the individual patient, subject, study group, species, tissue or even cell line.
- Membership in the MitoEAGLE network is open to all researchers sharing an interest in mitochondrial research and medicine
- » Join the COST Action CA15203 MITOEAGLE
- MitoEAGLE
- MiPsociety
- The MiPsociety is an international organization, based in Europe and operating world-wide and has become a legal body in 2011 continuing a tradition of rigorous mitochondrial bioenergetics; integrating molecular, cellular and organismic physiology and pathology.
- Membership is open to all researchers
- » MiP membership
- MiPsociety
How to get there
- There are daily flights in each direction between Oslo and Tromsø, flown by SAS and Norwegian (Please note that there are only a few flights on a Saturday)
- The same companies also offer some direct flights from Stockholm Arlanda, Copenhagen, and London Gatwick, but these are seasonal (so do check yourselves if these routes are operating and of interest).
- Arctic Airlink also offer direct flights to Tromsø from Luleå and Oulu. The nearest train station is Narvik.
- It is 3 1/2 hours’ drive from Tromsø, and it is connected to the Swedish, not the Norwegian, rail network (sj.se). There is a bus link from Narvik, but usually, the train does not meet the last bus to Tromsø.
- Training school participants arriving in Tromsø before October 20th can find accommodation on the official travel guide to Tromsø (https://www.visittromso.no/en/Troms%C3%B8%20Airport), which gives you an overview of the various hotels in the city, as well as transportation from the airport to the city center, and what to do in Tromsø.
- On Saturday morning (from 10:00 h), we will organize a meeting place at the UiT Campus for training school participants arriving throughout the day (information desk and temporary luggage storage).
- Here, you will also have access to Internet and, if needed, a quiet spot for work. Take a taxi from the airport to the university and ask the driver to stop at the main (west) entrance of the MH building (link to map). The meeting place will keep open until 21:00 h.
- In the city, luggage lockers are available on the 1st floor in the harbour terminal (link to map). These are card-operated lockers, and cost NOK 60 for a 24-hour period. Available during the terminal opening hours: 05.30-02.00 h.
- The registration desk opens at 21:00 h at Skarven Bar downtown Tromsø. This will be our assembly point until the Coastal Express arrives around midnight. We will walk from the bar to the harbor terminal, which is just a couple of minutes away (link to map).
Participants and abstracts - alphabetical order
Presentation | |
---|---|
Alves 2018 MiPschool Tromso E2 | Role for mitochondria on the response of highly proliferative and invasive bladder cancer cells to the combined inhibition of mTOR and SIRT1. |
Arago 2018 MiPschool Tromso | No abstract. |
Armand 2018 MiPschool Tromso | No abstract. |
Bajzikova 2018 MiPschool Tromso | No abstract. |
Bastos Sant'Anna Silva 2018 MiPschool Tromso C4 | Role of succinate in prostate cancer cells: uptake and mitochondrial respiratory function. |
Bello 2018 MiPschool Tromso | No abstract. |
Bergmeister 2018 MiPschool Tromso | No abstract. |
Boardman 2018 MiPschool Tromso D3 | High fat-load induces cardioprotection in hearts from obese mice. |
Cardoso 2018 MiPschool Tromso E2 | Concomitant respiration and ATP production measurements to analyse P»/O2 ratios at physiological normoxia. |
Crisostomo 2018 MiPschool Tromso C4 | Mitochondrion at the crosstalk between metabolic disease and dysfunction in male fertility? |
Dahdah 2018 MiPschool Tromso | No abstract. |
Detraux 2018 MiPschool Tromso | No abstract. |
Dubouchaud 2018 MiPschool Tromso | AMPK deficiency elicits changes in OXPHOS in heart mitochondria. |
Ferreira 2018 MiPschool Tromso | No abstract. |
Fischer 2018 MiPschool Tromso E2 | Analysis of mitochondrial function in iron deficiency anemia and iron overload conditions. |
Garipi 2018 MiPschool Tromso E2 | Phenotyping mitochondrial metabolism in Barrett’s metaplasia-dysplasia-adenocarcinoma sequence: respiratory capacity, extracelular proton flux and ROS production |
Gnaiger 2018 MiPschool Tromso A1 | Mitochondrial states and rates: 1. Electron transfer pathways and respiratory control. 2. Coupling control. |
Gnaiger 2018 MiPschool Tromso A2 | The protonmotive force and respiratory control. 1. Coupling of electron transfer reactions to vectorial translocation of protons. 2. From Einstein’s diffusion equation on gradients to Fick’s law on compartments. |
Goncalo Teixeira 2018 MiPschool Tromso C1 | Subchronic in vivo study for the evaluation of hepatic mitochondrial toxicity induced by silver nanoparticles. |
Handl 2018 MiPschool Tromso | No abstract. |
Harper 2018 MiPschool Tromso D1 | OXPHOS efficiency in skeletal and cardiac muscles: Proton leaks, ROS and glutathione redox. |
Harper 2018 MiPschool Tromso E1 | Deacetylation acceleration of BAT thermogenesis. |
Heiestad 2018 MiPschool Tromso | No abstract. |
Hoppel 2018 MiPschool Tromso D1 | Two populations of muscle mitochondria: heart and skeletal muscle. |
Hoppel 2018 MiPschool Tromso D2 | Mitochondrial function during ischemia/reperfusion injury. |
Huete-Ortega 2018 MiPschool Tromso E2 | High-resolution respirometry: new perspectives for the study of bioenergetics in algae and plants. |
Hyrossova 2018 MiPschool Tromso | No abstract. |
Iglesias-Gonzalez 2018 MiPschool Tromso E1 | Oscillations in mitochondrial ROS production during the early cell cycles in Xenopus embryos. |
Isola 2018 MiPschool Tromso C3 | AMPK deficiency elicits changes in OXPHOS in heart mitochondria. |
Jansen 2018 MiPschool Tromso C2 | Dietary and pharmacological treatment of diet-induced obese mice – impact on mitochondrial function. |
Jaskiewicz 2018 MiPschool Tromso | No abstract. |
Kampa 2018 MiPschool Tromso C2 | Cardioprotective flavoniods as a natural modulators of mitoBKCa channel. |
Kidere 2018 MiPschool Tromso E2 | Cytoplasmic hybrid cells as a model to characterize the OXPHOS system: control sample with glutamate metabolism defect. |
Krajcova 2018 MiPschool Tromso E2 | High-resolution respirometry to assess function of mitochondria in native homogenates of human heart muscle. |
Larsen 2018 MiPschool Tromso | Local organizer |
Li Puma 2018 MiPschool Tromso E2 | Fads2 exacerbates myocardial ischemia-reperfusion injury in mice: role of mitochondria. |
Ma 2018 MiPschool Tromso C1 | Cardiolipin synthesis in brown and beige fat mitochondria is essential for systemic energy homeostasis. |
Majtnerova 2018 MiPschool Tromso | No abstract. |
Makrecka-Kuka 2018 MiPschool Tromso E1 | Cardiac fatty acid oxidation: from in vitro to in vivo. |
Marstein 2018 MiPschool Tromso | No abstract. |
MartinsAD 2018 MiPschool Tromso E2 | Mitochondrial dynamics of human Sertoli cells under the effect of leptin and ghrelin. |
MartinsJD 2018 MiPschool Tromso C2 | Sweetheart: Cardiac consequences of fetal exposure to maternal gestational diabetes on the offspring mitochondrial function. |
Murray 2018 MiPschool Tromso E1 | OXPHOS protocols: understanding the patterns. |
Musiol 2018 MiPschool Tromso C4 | Alpha-tomatine as a novel membrane-permeabilizing agent for mitochondrial respiration measurements. |
Pedersen 2018 MiPschool Tromso | No abstract. |
Pereira 2018 MiPschool Tromso C1 | Obesity-induced mitochondrial hepatic changes during pregnancy. |
Puurand 2018 MiPschool Tromso E2 | Intracellular energy-transfer networks in health and disease – the results of oxygraphic studies. |
Schartner 2018 MiPschool Tromso | |
Schlattner 2018 MiPschool Tromso B1 | Mitochondrial kinases: key players in respiratory control and energy transfer. |
Schots 2018 MiPschool Tromso | |
Siewiera 2018 MiPschool Tromso E2 | Effect of metformin treatment on blood platelet bioenergetics and platelet function in STZ-diabetic and non-diabetic rats. |
Storder 2018 MiPschool Tromso E2 | Investigaton on the role of the mitochondiral deacetylase Sirtuin 3 in adipose tissue. |
Template 2018 MiPschool Tromso | |
Torp 2018 MiPschool Tromso C3 | Intracellular complement factor 3 in the heart – a link to metabolism? |
Truu 2018 MiPschool Tromso | No abstract. |
Tuncay 2018 MiPschool Tromso C2 | MitoTEMPO ameliorates hyperglycemia induced mitochondrial damage in cardiomyocytes. |
Vella 2018 MiPschool Tromso C4 | Exome analysis sheds light on mitochondrial disorders. |
Vendelin 2018 MiPschool Tromso B1 | Restrictions to intracellular diffusion of ATP and ADP in cardiomyocytes. |
Vendelin 2018 MiPschool Tromso D2 | Modeling actomyosin contraction in the heart muscle. |
Vendelin 2018 MiPschool Tromso E1 | Introducing a platform for primary kinetics data analysis. |
Vieira Ligo Teixeira 2018 MiPschool Tromso | No abstract. |
Vujacic-Mirski 2018 MiPschool Tromso C4 | Development of analytical assays for the detection and quantification of reactive oxygen and nitrogen species in an animal model of type 1 diabetes - ROS formation involving mitochondrial and NADPH oxidase. |
Wiesner 2018 MiPschool Tromso E1 | Aging-related accumulation of mitochondrial DNA deletions in skeletal muscle occurs preferentially in Type IIb fibers – high mitophagic flux protects Type I fibers. |
Wuest 2018 MiPschool Tromso D3 | Metabolic flexibility and mitochondrial function in the diabetic heart. |
Zdrazilova 2018 MiPschool Tromso C4 | Bioenergetic characterization of skin fibroblasts from patients with congenital disorders of glycosylation. |
Zobalova 2018 MiPschool Tromso | No abstract. |
Support
MitoEAGLE Scholarships
- Eligibility: Participants from all COST countries can apply - MitoEAGLE network.
- Late registration: The COST MitoEAGLE grant is a financial support to cover part of the local costs (accommodation, meals).
- » Notification of MitoEAGLE scholarships for late registrations will be given until September 20.
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