creating a
healthier future

3rd Workshop on Neuroengineering: Decoding Neural Information

08-09 April 2019 | i3S, Porto

 

Neuroengineering is a multidisciplinary field with the goal of addressing neuroscience problems with methodologies that go well beyond molecular and cellular biology: by combining neuroscience with engineering fields such as computer science, information theory, electronics, nanomaterials, among others, neuroengineering creates new ways to reveal, repair and even enhance human brains. This workshop aims at promoting an intellectually stimulating environment where new ideas can be exchanged and new collaborations can be forged. By integrating hands-on practical sessions, the workshop also gives the possibility for the interested participants to try basic techniques used in neuroengineering.

We look forward to seeing you at the workshop

 

Organizer: Paulo de Castro Aguiar, INEB/i3S | Co-Organizer: Miguel Vieira, UCP

 

 

Program

First day | 8th April: Lectures covering different topics in neuroengineering.

Second day, optional | 9th April: Hands-on practical sessions on basic lab techniques in neuroengineering.

The hands-on practical sessions are targeted for students (MSc and PhD), but are in fact open to everyone. Every practical session has a duration of 3h and each participant can only choose (register) one hands-on practical session. The list of available practical sessions is presented below.

Please notice that the number of available seats in some sessions are very low. The minimum number of participants per session is 2.


Schedule

 

First day | 8th April

09:50 Welcome

 

10:00 The dawn of bottom-up neuroscience: how to build, modify and analyze controlled neural networks
Janos Vörös
, ETH Zürich

 

10:45 Intercepting axonal communication: new algorithms and new 3D structured microelectrodes for in vitro studies
Paulo Aguiar,
INEB/i3S

 

11:30 Coffee break

 

12:00 Huntington disease brain on-a-chip: microfluidic/microelectrode array to study activity-dependent intracellular dynamics in neuronal networks
Frédéric Saudou, Grenoble Institute of Neurosciences

 

12:45 Organic technology for neuroprosthetic vision
Diego Ghezzi
, Medtronic Chair in Neuro Engineering, EPFL

 

13:30 Lunch

 

14:30 Engineered neuronal assemblies and functional connectivity analysis
Sergio Martinoia
, University of Genova

 

15:15 Imaging whole-brain neural activity dynamics in larval zebrafish
Michael Orger
, Champalimaud Neuroscience Programme

 

16:00 Meet the Speakers

 

16:30 Coffee break

 

17:00 In vivo recordings and neural manipulation to test hippocampal-medial mesocortex interactions during choice behaviors
Miguel Remondes, IMM

 

17:45 The Connectome: a comprehensive framework for studying information flow in the brain
Hugo Ferreira
, IBEB/FCUL

 

18:30 Concluding Remarks

 

Second day | 9th April

09:30-12:30 Hands-on practical morning session

14:00-17:00 Hands-on practical afternoon session

 


Hands-on Practical Sessions

 

S1 – Basics of Neuronal Cell Cultures

[Responsible: Cátia Lopes, NCN - INEB/i3S]

Cell culturing techniques are widely used in neuroengineering studies and have significantly improved our understanding of the physiological and pathological processes of living organisms. This workshop session is intended to provide an introductory training in the basic requirements for successful cell culturing. With this hands-on training session, the participants will get acquainted with a number of valuable resources and guidelines required to establish and maintain a cell culture, as well as the basic principles of sterile technique and laboratory safety issues.

 

S2 – Memristive artificial synapses: from device principles to neuromorphic applications

[Responsible: Catarina Dias, IFIMUP]

Neuromorphic devices use the brain's structure and operation principles as a promising solution for modern computational storage and processing demands. Memristors, a new class of electronic devices, resemble properties similar to neural synapses. They behave like resistors whose resistance depends on the current that passed through the device. This session will start with an introduction to the memristor and then followed by the electrical characterization of some real examples. Finally, the results will be analyzed to characterize and distinguish different devices.

 

S3 – Principles of patch-clamp electrophysiology (FULL)

[Responsible: Liliana Luz, IBMC/i3S]

Electrophysiology is the biomedical field dealing with the study of the electrical properties of cells and tissues. The patch-clamp technique is a major tool in electrophysiology which allow us to study cell excitability, functions and pharmacology of ion channels. Understanding how neurons respond to electrical stimuli is an essential element in the design of systems capable of modulating the activity in neuronal populations. In this practical session participants will learn the very basics of patch-clamp electrophysiology and will have to possibility to record the activity of neurons subject to electrical stimulation.

 

S4 – Introduction to the NEURON modeling software – in silico neuroscience and detailed simulations of neurons in a computer

[Responsible: Paulo Aguiar, NCN - INEB/i3S]

Neurons are cells specialized in transmission, storage and processing of information. Understanding the complexities of neuronal dynamics in normal conditions, in order to devise correction strategies in pathological conditions, requires detailed modeling and computer simulations. This hands-on practical session gives an introduction to the NEURON simulation environment, a well-established tool for in silico neuroscience and the workhorse software of the Human Brain Project. Participants will learn how to perform biophysically detailed simulations of single neurons and small neuronal circuits. Participants are requested to bring their laptop for the session.

 

S5 – Principles of multielectrode arrays (MEAs) electrophysiology (FULL)

[Responsible: José Mateus, NCN - INEB/i3S]

Multielectrode array (MEA) technology is at the forefront of recording electrical activity from large neuronal ensembles. MEAs enable electrophysiological recordings of hundreds of neurons simultaneously, thus are of great use in both basic and clinical/applied neuroscience. Furthermore, different microelectrodes can be used to both record and stimulate neuronal activity in the same experiment. In this practical session, the participants will get acquainted with the principles of MEA experiments and have the possibility to evoke and record extracellular signals from in vitro neuronal networks.

 

S6 – Imaging neuronal activity with Calcium dyes (FULL)

[Responsible: Miguel Aroso, NCN - i3S/INEB]

During electric activity of neurons, the cytoplasmatic calcium concentration rises transiently to values that can be 100x higher than in resting state. Calcium dyes are used to monitor neuronal activity by accessing these intracellular changes of Ca2+ concentration. The calcium dyes are typically organised by two parts: a chelator that binds to free Ca2+ and a fluorophore that emits fluorescent light and when it bind to Ca2+ the emitted fluorescence increases. Fluorescence is commonly recorded by an optical imaging system (microscope) with a high-speed camera, however, advanced imaging processing methods are required to extract precise neuronal activity measurements. In this session, participants will have the opportunity to record neuronal cell cultures labelled with a commercial calcium dye and analyse the acquired data with a software developed in-house.

 

S7 – Introduction to basic concepts of neuronal morphometric analysis in imageJ

[Responsible: Ana Gerós, NCN - INEB/i3S]

In neurons, shape and function are intimately related. Quantification of morphological characteristics (morphometrics) is therefore an important step in the evaluation of many experimental conditions. This practical session gives an introductory crash course on neuronal morphometric analysis for people with little or no knowledge in the subject. The following case studies with 2D fluorescence images, and associated image analysis workflows, will be addressed: a) neurite tracing and total fiber length; b) detecting and counting spines; c) automatic cell body segmentation and area calculation; d) Sholl analysis; in addition to a few others. Participants should have already some experience with imageJ/Fiji.

 

Speakers

Diego Ghezzi

Diego Ghezzi

EPFL, CH

        Frédéric Saudou

Frédéric Saudou

Grenoble Institut Neurosciences

         
Hugo Ferreira

Hugo Ferreira

IBEB/FCUL

  Janos Vörös

Janos Vörös

ETH Zürich

         
Michael Orger

Michael Orger

Champalimaud Foundation

        Miguel Remondes

Miguel Remondes

IMM

         
Paulo Aguiar

Paulo Aguiar

i3S / INEB

        Sergio Martinoia

Sergio Martinoia

University of Genova

 

 

Registration

A participant can register for the lectures only (8th April), for a hands-on session only (9th April), or for both lectures and one hands-on session. The registration fees include the coffee breaks and lunch (on 8th April only) and the necessary hands-on session materials. Please notice that the number of seats is limited (for both lectures and practical sessions). Participation will be confirmed on a first come, first served basis, upon confirmation of registration fee payment.
The time slot (morning or afternoon) for each practical session is subject to confirmation. This information will be provided to the participants upon registration.

 

REGISTRATION FEES:

Early bird registration: until March 18th 2019 | Payment deadline: March 21st 2019

Hands-On Session only: 40€ (for one hands-on session)

Lectures only: 20€

Full workshop: 50€

 

Regular registration: Between March 19th until March 25th 2019 | Payment deadline: 29th March 2019

Hands-On Session only: 60€ (for one hands-on session)

Lectures only: 40€

Full workshop: 70€

 

 

PAYMENT DETAILS

Please identify your name clearly and the Registration ID when ordering the transfer and send us a copy of the transfer receipt to events@i3s.up.pt.

The receipts will be issued only if requested and amendments will not be accepted.

Full payment of costs should be made in EURO (payments in any other currency will not be accepted).

Currency exchanges or bank fees have to be paid by the registrant. In case of cancellation, the registration fee will not be refunded.

 

BANK DETAILS

Bank Holder Name: INEB - Instituto Nacional de Engenharia Biomédica

Bank: Millennium BCP

Address Bank: Palácio do Comércio - Rua Sá da Bandeira, 501 - 4000-436 Porto Portugal

IBAN: PT50 0033 0000 0388 0160 11604

Account: 03880160116

Swift (BIC): BCOMPTPL

INEB VAT number: 502 312 220

Sponsors

A joint initiative between i3S and the Discoveries CTR

PRINCIPAL SPONSOR

 


SCIENTIFIC PLATFORMS   SPONSORS
     
                

   
   
     

 

Contacts

Events Management Office
Rua Alfredo Allen 208 | 4200-135 Porto, Portugal
Email: events@i3s.up.pt | Tel: +351 220 408 811 | Cell/ Mobile: +351 964 013 945