International Training in Reproductive Sciences and Technologies
June 3 – 9, 2012
32nd Annual ASRI Congress, Hamburg
Joint International Congress of the American Society for Reproductive Immunology (ASRI) and the European Society for Reproductive Immunology (ESRI) 2012.
http://www.asri-esri-2012.de
http://www.repromedizin.de/fileadmin/veranst/dgrmschool/Intrest_2012_A4.pdf
The event takes place over one and a half days and features...
Monday 9th July: an afternoon of 15-minute presentations featuring new data selected from delegate submissions. If you would like to present new data to the meeting, please select the appropriate option when booking. Then email your title and abstract to the Centre’s Administratoramc210@cam.ac.uk to arrive no later than Friday 1st June.
Tuesday 10th July: a themed day focused on hypoxia: sensing and consequences, featuring experts in the fields of molecular physiology and pathology, genetics, and reproductive biology.
There will be a formal dinner on the evening of Monday 9th July at Magdalene College. Numbers are strictly limited so please book early to avoid disappointment.
Click here to view the full programme.
This year we have introduced an electronic booking system. Please register online to book your place.
CTR members:
Registration is free for CTR members
Dinner at Magdalene College costs £20 (rising to £30 on bookings made after 4th June).
CTR Members please note: If you do not wish to attend the dinner, you are still required to register and book. You will be issued with a booking confirmation but you will not be charged. Click here to book your place.
Non-members:
£75 Early Bird Registration Fee (applies up to 4th June.) After 4th June, the cost is £150.
Dinner at Magdalene College costs £25 (rising to £30 on bookings made after 4th June.)
Click here to book your place.
There is provision for delegates to bring a poster for display, which you are very welcome to do. If you wish to bring a poster, please contactamc210@cam.ac.uk to enable us to assess how much space to allocate.
Since there is no provision for accommodation at the Centre for Mathematical Sciences, please arrange your own Hotel, College or Bed & Breakfast via one of the following websites:
http://www.conferencecambridge.com/accommodation
http://www.cambridgerooms.co.uk
http://www.cambridgebedbreakfasts.co.uk
http://www.visitcambridge.org/VisitCambridge/WhereToStay.aspx
Centre for Mathematical Sciences
Wilberforce Road
Cambridge CB3 0WA
Telephone: +44 1223 765 000
The Centre for Mathematical Sciences is located on Wilberforce Road, off Madingley Road. The Centre can also be reached from Clarkson Road, off Grange Road (not for cars).
The venue is a 15-20 minute walk from the City centre. Please allow sufficient travelling time.
Parking on site is extremely limited so we do not recommend bringing your car. Instead please travel by public transport, walk or use pedal power. Cycle parking is provided in designated areas in the Centre’s carpark.
Disabled parking may be booked via the CTR Administrator: amc210@cam.ac.uk
By train and bus
There are frequent services to Cambridge from King's Cross and Liverpool Street stations in London.
The site is approximately three miles from the railway station. If you take a taxi from the station ask to be dropped at Clarkson Road. The fare should be in the region of £7.50.
Details of the bus service (Citi 4 and Uni 4) linking the University sites on the west of Cambridge to the city centre and Addenbrooke's can be found at http://www.admin.cam.ac.uk/offices/embs/travel/bus/
The Park and Ride Red bus (77) from Madingley Road stops near the Centre for Mathematical Sciences.
Stagecoach operate the U4 (University bus) and the C4 which both serve the Centre for Mathematics site, stopping on both Madingley Road and Grange Road.
National Express provides coach services to Cambridge from Central London, and from many UK airports:http://www.nationalexpress.com/home.aspx
By car
Parking on site is extremely limited so we do not recommend bringing your car. Motorists should use the Park & Ride carpark at Madingley Road, which is one mile away, just off the M11 at Junction 13. http://www.cambridgeshire.gov.uk/transport/around/parkandride/madingleyroad/
The Park and Ride Red bus (77) stops near the Centre for Mathematical Sciences.
More travel information, maps and a site plan of the Centre for Mathematical Sciences can be found here.
There are disabled parking spaces at the Centre for Mathematical Sciences (accessed through the entrance on Wilberforce Road). Please book your space via the CTR Administrator, amc210@cam.ac.uk
The presentations will be held in the Wolfson Room, which is one floor below reception. Disabled toilets are also on this floor. The lift to the Wolfson Room is accessed via Pavilion G. Please see a member of the Centre’s staff who will be happy to direct you.
A formal dinner will take place on the evening of Monday 9th at Magdalene College Hall, commencing at 7pm. A cash bar will be available for diners only from 5.30pm. Numbers are strictly limited so please book early to avoid disappointment.
We have tried to answer any questions you might have in the information given above. However, if you still have a query about the CTR Annual Trophoblast Meeting, please contact the CTR Administrator, amc210@cam.ac.uk.
• Evidence
• Programs
• Policy
This scholarship is to support students with excellent undergraduate records who complete their Honours training at WCHRI. Students can be enrolled through any of the South Australian Universities.
Stipend will be $2000.
Deadline for application is the end of October each year.
Submission details and selection criteria available on request.
2006 - Xian Wang (Flinders University)
2007 - Lucy Simmonds (University of Adelaide)
2008 - Wan Ilma Dewiputri Wan Burhanuddin (University of Adelaide)
Oportunidad para Profesionales Jovénes para trabajar en eSalud en América Latina y el Caribe
FECHA LÍMITE PARA LAS APLICACIONES: 6 JUNIO 2011
“…Este es será el siglo de las redes, de la conectividad y la interdependencia, que nos permitirá superar las barreras del espacio y del tiempo y que abrirá posibilidades inimaginables a la humanidad. Si estimulamos a esas redes para que multipliquen exponencialmente el capital social disponible, que vinculen a las personas y a las instituciones en una gran malla de sostén e inclusión de todos los habitantes del continente, habremos dado un paso fundamental para que fluya el conocimiento y la experiencia en nuevas modalidades de intercambio de la cooperación técnica para el desarrollo humano sostenible…. ”.
Discurso de la Dra. Mirta Roses Periago en su Inauguración como Directora de la Organización Panamericana de la Salud, y Directora Regional para las Américas, 31 de enero de 2003
·¿Qué es el Proyecto Innovación y eSalud Pública y Equidad para América Latina y el Caribe(eSAC)?
¿Quiénes son los profesionales jóvenes (YPs)?
¿Cuáles son los beneficios de ser seleccionado como uno de los Profesionales jóvenes, (YPs)?
·¿Cómo son seleccionados los profesionales jóvenes (YPs)?
·¿Como aplicar?
·Información adicional
http://new.paho.org/ict4health/index.php?option=com_content&view=article&id=46&Itemid=45&lang=es
***
Perhaps the most famous use of taurine in recent years has been in the energy drink Red Bull. Originating on college campuses and in nightclubs in Austria, the product quickly spread. The drink's marketing leans heavily on its unusual ingredient, and so integral is the substance to the brand that even the name derives from it - taurus is Latin for bull (as taurine was first isolated from ox bile in 1827). Red Bull promises that the taurine, along with caffeine and, in its original form, a great deal of sugar, will help to 'vitalise body and mind'.
However, other researchers' findings support the company's claims. Seidl et al [2] report a double blind placebo controlled survey on a number of university students who demonstrated increased motor response and alertness compared to those receiving the placebo. Unfortunately the test did little to determine which of the drink's ingredients were responsible for the effects.
Although by the strictest definition, taurine is not an amino acid as it does not contain a carboxylic acid COOH group [3], it is generally referred to as one in published literature [4, 32,33,37]. At pH 7, the molecule exists as a zwitterion, in which the NH2 end of the molecule exists as NH3+ and the opposite end as SO3-. This gives the molecule two polar ends and a non-polar carbon chain centre, allowing for a great many possible binding interactions. Unusually for a biological compound, taurine does not exhibit chirality.
Taurine - (2-aminoethane sulphonic acid) [1]
Taurine is synthesised by the human body, primarily in the liver by oxidation followed by decarboxylation of the amino acid cysteine.
The biosynthesis of taurine from cysteine in the liver [5].
Taurine is one of a group of organic compounds which has been formed in experiments designed to simulate early-Earth conditions along with electrical discharges to simulate lightning. This result is often cited as evidence for the ease with which sulfur-containing biological molecules could be naturally synthesised under prebiotic conditions [6]. The conclusion is somewhat controversial, however, as the reaction occurred because of the presence of large concentrations of methane and ammonium hydroxide, the abundance of which on prebiotic Earth is questionable [7].
With a few exceptions, liver-synthesised taurine is not incorporated into polypeptides but is found free, lending it a unique set of properties, including a separate intercell transport mechanism and an independence from protein synthesis and catabolism [8]. Taurine has been linked to a wide range of bodily functions and Stapleton et al (1998) list roles in "osmoregulation, antioxidation, detoxification and stimulation of glycolysis and glycogenesis". The synthesis pathway of taurine is especially active in the early stages of life, and taurine is found in breast milk, suggesting that it is particularly vital at this stage. Taurine also plays a role in muscle contraction, where it enhances the ability of the muscles to generate force by catalysing the uptake and release of calcium ions [9].
Experiments on rats have also yielded evidence of a very substantial role in detoxification in the liver - Waters et al [10] report that high doses of taurine administered before or soon after ingestion of an overdose of paracetemol protected the livers of rats from hepatotoxcity and serious liver damage from the drugs. Although the idea has yet to progress to any form of human trial, the prophylactic and therapeutic benefits of the substance in cases of paracetemol overdose are promising .
Taurine is necessary for normal skeletal muscle functioning in humans and mice [13]. Cats cannot synthesise taurine, and so need it added as supplements in their diets. Without it, they suffer conditions such as blindness, hair loss and tooth decay. Taurine is also essential in the early development of many types of perching birds. Parent birds with new offspring often seek out spiders (which are rich in taurines) with which to feed their young. so, in this case, taurine really does give them wings!
1. Kim W., "Debunking the Effects of Taurine in Red Bull Energy Drink", Nutrition Bytes, 9, (2003) 6.
2. Seidl R. et al, "A Taurine and Caffeine-containing drink stimulates cognitive performance and well-being", Amino Acids, 19, (2000) 635.
3. Sharp D., Dictionary of Chemistry (Abridged), 3rd Edition, Penguin Books, 2003.
4. Stapleton P. et. al, "Host defense - a role for the amino acid taurine?", J. Parenteral and Enteral Nutrition, 22, (1998) 42.
5. Moss G., "Taurine Biosynthesis", http://www.chem.qmul.ac.uk/iubmb/enzyme/reaction/misc/taurine.html, Queen Mary University of London, 1992.
6. Ferris J., "Chemical markers of Prebiotic Chemistry in Hydrothermal systems", in Origin of Life and Evolution of Biospheres V.22 Numbers 1-4, ed. N Holm, Springer, Netherlands, Jan. 1992, p.120.
7. Wigley T., Nature, 291, (1981) 213.
8. Chiarla C. et al, "The Relationship between Plasma Taurine and Other Amino Acid Levels in Human Sepsis", J. of Nutrition, 130, (2000) 2222.
9. K. Harrison, "Taurine", http://www.3dchem.com/molecules.asp?ID=22, (2002).
10. Waters E. et al, "Role of taurine in preventing acetaminophen-induced hepatic injury in the rat", Am. J. Physiol. Gastrointest. Liver Physiol., 280, (2001) 1274.
11. Murphy B. et al, "Taurine as an Anti-Manic Agent", (2005) http://www.clinicaltrials.gov/ct/show/NCT00217165
12. Tsuboyama-Kasaoka et al, "Taurine (2-Aminoethanesulfonic Acid) Deficiency Creates a Vicious Circle Promoting Obesity", Endocrinology, 147, (2006) 3276.
13. Wikipedia - taurineIn a match that pitted video game players against the best known computer program designed for the task, the gamers outperformed the software in figuring out how 10 proteins fold into their three-dimensional configurations.
Proteins are essentially biological nano-machines that carry out myriad functions in the body, and biologists have long sought to understand how the long chains of amino acids that make up each protein fold into their specific configurations.
In May 2008, researchers at the University of Washington made a protein-folding video game called Foldit freely available via the Internet. The game, which was competitive and offered the puzzle-solving qualities of a game like Rubik’s Cube, quickly attracted a dedicated following of thousands of players.
The success of the Foldit players, the researchers report in this week’s issue of Nature, shows that nonscientists can collaborate to develop new strategies and algorithms that are distinct from traditional software solutions to the challenge of protein folding.
The researchers took pains to credit the volunteers who competed at Foldit in the last two years, listing “Foldit players” at the end of the report’s author list and noting that more than 57,000 players “contributed extensively through their feedback and gameplay.”
Zoran Popovic, a computer scientist at the University of Washington who was a lead author of the paper, said, “If things go according to plan, not too long from now, such massive author lists should be commonplace.” Foldit begins with a series of tutorials in which the player controls proteinlike structures on a computer display. In the game, as structures are modified, a score is calculated based on how well the protein is folded. Players are given a set of controls that let them do things like “shake,” “wiggle” and “rebuild” to reshape the backbone and the amino acid side shapes of a specific protein into a more efficient structure.
A list of top scores for each puzzle is posted so that players can compare their results. Players may also collaborate in teams, tracking progress on a separate list of group scores.
The protein-folding problem can be solved by computers using statistical and related software algorithms, but it takes an immense amount of processing power.
“The problem is that these proteins are far, far more complex than a robotic arm, and can ‘fold’ in time frames measured in billionths of a second,” Duke Ferris, founder of the GameRevolution Web site, wrote recently. “It’s like trying to solve a million-sided Rubik’s Cube while it also spins at 10,000 r.p.m. And that’s for just one ‘fold.’ ”
In a comparison involving 10 separate protein-folding puzzles, video game players matched the results generated by software solutions in three of the puzzles, outperformed them in five cases and found significantly better solutions in two others, according to the scientists.
In addition to the acuity of human pattern-recognition skills, the researchers noted that players outperformed the best software tools in other ways as well, writing: “Humans use a much more varied range of exploration methods than computers. Different players use different move sequences, both according to the puzzle type and throughout the duration of a puzzle.”
The Foldit project was inspired by the volunteers who were contributing the downtime on their home computers to power a protein-folding program called Rosetta@home. The computer donors could see the progress of the program on their screens, and they began to note inefficiencies in the software’s folding approach. That led the scientists to look for ways to systematically harness the skills of the human volunteers.
Animals like newts and zebra fish can regenerate limbs, fins, even part of the heart. If only people could do the same, amputees might grow new limbs and stricken hearts be coaxed to repair themselves.
But humans have very little regenerative capacity, probably because of an evolutionary trade-off: suppressing cell growth reduced the risk of cancer, enabling humans to live longer. A person can renew his liver to some extent, and regrow a fingertip while very young, but not much more.
In the first of the two new approaches, a research group at Stanford University led by Helen M. Blau, Jason H. Pomerantz and Kostandin V. Pajcini has taken a possible first step toward unlocking the human ability to regenerate. By inactivating two genes that work to suppress tumors, they got mouse muscle cells to revert to a younger state, start dividing and help repair tissue.
What is true of mice is often true of humans, and although scientists are a long way from being able to cause limbs to regenerate, the research is attracting attention. Jeremy Brockes, a leading expert on regeneration at University College London, said the report was “an excellent paper.” Though there is a lot still to learn about the process, “it is hard to imagine that it will not be informative for regenerative medicine in the future,” he said.
In recent years, most research in the field of regenerative medicine has focused on the hope that stem cells, immature cells that give rise to any specific type of cell needed in the body, can somehow be trained to behave as normal adult cells do. Nature’s method of regeneration is quite different in that it starts with the adult cells at the site of a wound and converts the cells to a stemlike state in which they can grow and divide.
The Stanford team has taken a step toward mimicking the natural process. “What I like is that it’s built on what’s happening in nature,” Dr. Blau said. “We mammals lost this regenerative capacity in order to have better tumor suppression, but if we reawaken it in a careful way we could make use of it in a clinical setting.”
Dr. Pomerantz, a clinician, hopes the technique can be applied to people, though many more animal experiments need to be done first. “We have shown we can recapitulate in mammalian cells behavior of lower vertebrate cells that is required for regeneration,” he said. “We would propose using it in amputations of a limb or part of a limb or in cardiac muscle.” After a heart attack, the muscle cells do not regenerate, so any method of making them do so would be a possible treatment.
Interfering with tumor suppressor genes is a dangerous game, but Dr. Pomerantz said the genes could be inhibited for just a short period by applying the right dose of drug. When the drug has dissipated, the antitumor function of the gene would be restored.
Finding the right combination of genes to suppress was a critical step in the new research. One of the two tumor suppressor genes is an ancient gene, known as Rb, which is naturally inactivated in newts and fish when they start regenerating tissue. Mammals possess both the Rb gene and a backup, called the Arf gene, which will close down a cancer-prone cell if Rb fails to do so.
The Stanford team found that newts did not have the Arf backup gene, which mammals must have acquired after their lineage diverged from that of amphibians. This suggests that the backup system “evolved at the expense of regeneration,” the Stanford researchers say in Friday’s issue of Cell Stem Cell.
The Stanford team shut off both Rb and Arf with a chemical called silencing-RNA and found the mouse muscle cells started dividing. When injected into a mouse’s leg, the cells fused into the existing muscle fibers, just as they are meant to.
The Stanford researchers have learned how to block two genes thought to inhibit the natural regenerative capacity of cells, but it is somewhat surprising that the regenerative mechanism should still exist at all if mammals have been unable to use it for 200 million years. “One school of thought is that regeneration is a default mechanism and doesn’t require its own program,” Dr. Pomerantz said.
Dr. Brockes believes that this is true in part. Regeneration “depends on a largely conserved cellular machinery,” he said, meaning that it is present in all animals. The machinery comes into play in wound healing and tissue maintenance. But specific instances of regeneration, like regrowing a whole limb, are invoked by genes specific to various species. He has found a protein specific to salamanders that coordinates regrowth of a salamander limb.
If the regeneration of a whole limb is a special ability that salamanders have evolved, then humans would not have any inherent ability to do the same. “I would beware of suggesting that this sort of manipulation is capable of unlocking ‘the newt within,’ ” Dr. Brockes said.
A second, quite different approach to regenerating a tissue is reported in Friday’s issue of Cell by Deepak Srivastava and colleagues at the University of California, San Francisco. Working also in the mouse, they have developed a way of reprogramming the ordinary tissue cells of the heart into heart muscle cells, the type that is irretrievably lost in a heart attack.
The Japanese scientist Shinya Yamanaka showed three years ago that skin cells could be converted to embryonic stem cells simply by adding four proteins known to regulate genes. Inspired by Dr. Yamanaka’s method, Dr. Srivastava and his colleagues selected 14 such proteins and eventually found that with only three of them they could convert heart fibroblast cells into heart muscle cells.
To make clinical use of the discovery, Dr. Srivastava said he would need first to duplicate the process with human cells, and then develop three drugs that could substitute for the three proteins used in the conversion process. The drugs could be loaded into a stent, a small tube used in coronary bypass operations. With the stent inserted into a heart artery, the drugs would convert some of the heart’s tissue cells into heart muscle cells.
Some researchers hope that with Dr. Yamanaka’s method of turning skin cells into embryonic stem cells, those stem cells can be converted into usable heart muscle cells. One problem with this approach is that any unconverted embryonic stem cells may form tumors. Dr. Srivastava’s method sidesteps this problem by avoiding the stem cell stage.
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