Placeholder Content Image

Record-breaking "oldest" twin babies born

<p>The world's "oldest" twin babies have been born more than 30 years after being frozen as embryos.</p> <p>They could well be the longest-frozen embryos to ever result in a live birth, according to official records.</p> <p>Lydia and Timothy Ridgeway were welcomed into the world on October 31st 2022, three decades after the embryos were created for an anonymous married couple using IVF on April 22nd 1992.</p> <p>Lydia and Timothy's parents, Philip and Rachel, were never expecting to set a record as their fifth and sixth children were born. </p> <p>"We liked the idea that we are saving lives that are trapped,” Philip, 35 and a software developer, told <a href="https://nypost.com/2022/11/21/twins-lydia-and-timothy-ridgeway-already-age-30-at-birth/" target="_blank" rel="noopener">The New York Post</a>.</p> <p>The couple chose the oldest available option from National Embryo Donation Center (NEDC), a Knoxville, Tennessee, non-profit that provides donated embryos to couples wanting kids. </p> <p>“We knew basic information [about the genetic parents] such as height and weight, but we weren’t using that [as criteria] how we were going to choose,” said Rachel, a 34-year-old stay-at-home mom near Portland, Oregon.</p> <p>But they were more interested in, as Rachel put it, “How long have {the embryos} been waiting — which ones were waiting for parents to come and get them?”</p> <p>“When we went into this process, we wanted to find the embryos that were overlooked or most unwanted,” Rachel said. “We were looking for embryos that needed a home because they had been overlooked.” </p> <p>The process is sometimes referred to as “embryo adoption”, and is a recent phenomenon within the Evangelical Christian community in the Unites States. </p> <p>“The idea of giving birth to your adopted child was fantastic to me,” said Rachel.</p> <p>Philip would have been five years old when the embryos were first frozen, to put their age into perspective.</p> <p>"There is something mind-boggling about it," Philip told <a href="https://edition.cnn.com/2022/11/21/health/30-year-old-embryos-twins/index.html">CNN</a>.</p> <p><em>Image credits: The Ridgeway family</em></p>

Family & Pets

Placeholder Content Image

Scientists have mimicked an embryo’s heart to unlock the secrets of how blood cells are born

<p>Stem cells are the starting point for all other cells in our bodies. The <a href="https://www.eurostemcell.org/blood-stem-cells-pioneers-stem-cell-research" target="_blank" rel="noopener">first such cells to be found</a> were blood stem cells – as the name suggests, they give rise to different types of blood cells.</p> <p>But there’s much we don’t know about how these cells develop in the first place. In a study published today in <a href="https://doi.org/10.1016/j.celrep.2022.111339" target="_blank" rel="noopener">Cell Reports</a>, we have shown how a lab simulation of an embryo’s beating heart and circulation lead to the development of human blood stem cell precursors.</p> <p>The tiny device mimics embryonic blood flow, allowing us to directly observe human embryonic blood formation under the microscope. These results may help us understand how we can produce life-saving therapies for patients who need new blood stem cells.</p> <h2>Growing life-saving therapies in the lab</h2> <p>To treat aggressive blood cancers such as leukaemia, patients often need extremely high doses of chemotherapy; a <a href="https://www.cancer.nsw.gov.au/myeloma/diagnosis-and-treatment/treatment/types-of-treatment/stem-cell-transplant#:%7E:text=A%20stem%20cell%20transplant%20involves%20killing%20blood%20cells,they%20are%20collected%20beforehand%20and%20kept%20in%20storage." target="_blank" rel="noopener">blood stem cell transplant</a> then regenerates blood after the treatment. These are life-saving therapies but are restricted to patients who have a suitable tissue-matched donor of blood stem cells.</p> <p>A way around this problem would be to grow more blood stem cells in the lab. Unfortunately, past experiments have shown that harvested adult blood stem cells lose their transplantation potential if grown in the lab.</p> <p>The discovery of <a href="https://en.wikipedia.org/wiki/Induced_pluripotent_stem_cell" target="_blank" rel="noopener">induced pluripotent stem cells</a> – stem cells made out of adult cells – in 2006 led to a promising new approach. Induced pluripotent stem cells are made from the patient’s own cells, so there is no problem with tissue rejection, or the ethical issues surrounding the use of IVF embryos.</p> <p>These cell lines are similar to embryonic stem cells, so they have the potential to form any tissue or cell type – hence, they are “pluripotent”. In theory, pluripotent stem cell lines could provide an unlimited supply of cells for blood regeneration because <a href="https://en.wikipedia.org/wiki/Immortalised_cell_line" target="_blank" rel="noopener">they are immortalised</a> – they can grow in the lab indefinitely.</p> <p>But the development of processes to allow us to grow particular types of tissues, organs and cell types – such as blood – has been slow and will take decades to advance. One must mimic the complex process of embryogenesis in the dish!</p> <h2>Engineering an embryonic heart</h2> <p>Current understanding of how embryonic blood stem cells develop is based on animal models. Experiments with anaesthetised zebrafish embryos have shown that blood stem cells arise in the wall of <a href="https://pubmed.ncbi.nlm.nih.gov/20154733/" target="_blank" rel="noopener">the main blood vessel, the aorta</a>, shortly after the first heartbeat. For ethical reasons, it’s obvious this type of study is not possible in human embryos.</p> <p>This is why we wanted to engineer an embryonic heart model in the lab. To achieve this, we used <a href="https://www.elveflow.com/microfluidic-reviews/general-microfluidics/a-general-overview-of-microfluidics/" target="_blank" rel="noopener">microfluidics</a> – an approach that involves manipulating extremely small volumes of liquids.</p> <p>The first step in generating blood stem cells from pluripotent stem cells is to coax the latter to form the site where blood stem cells start growing. This is known as the AGM region (aorta-gonad-mesonephros) of the embryo.</p> <p>Our miniature heart pump and circulation (3 by 3 centimetres) mimics the mechanical environment in which blood stem cells form in the human embryo. The device pumps culture media – liquids used to grow cells – around a microfluidic circuit to copy what the embryo heart does.</p> <h2>A step closer to treatment</h2> <p>Once we got the cells to form the AGM region by stimulating cells on day two of starting our cell culture, we applied what’s known as pulsatile circulatory flow from day 10 to day 26. Blood precursors entered the artificial circulation from blood vessels lining the microfluidic channels.</p> <p>Then, we harvested the circulating cells and grew them in culture, showing that they developed into various blood components – white blood cells, red blood cells, platelets, and others. In-depth analysis of gene expression in single cells showed that circulatory flow generated aortic and blood stem precursor cells found in the AGM of human embryos.</p> <p>This means our study has shown how pulsatile circulatory flow enhances the formation of blood stem cell precursors from pluripotent stem cells. It’s knowledge we can use in the future.</p> <p>The next step in our research is to scale up the production of blood stem cell precursors, and to test their transplant potential in immune-deficient mice that can accept human transplants. We can do this by using large numbers of pluripotent stem cells grown in bioreactors that also mechanically stimulate blood stem cell formation.</p> <p>If we can easily produce blood stem cells from pluripotent stem cell lines, it would provide a plentiful supply of these cells to help treatments of cancer or genetic blood diseases.</p> <p><strong>This article originally appeared on <a href="https://theconversation.com/scientists-have-mimicked-an-embryos-heart-to-unlock-the-secrets-of-how-blood-cells-are-born-190530" target="_blank" rel="noopener">The Conversation</a>.</strong></p> <p><em>Image: UNSW</em></p>

Body

Placeholder Content Image

66 million-year-old perfectly preserved dinosaur embryo found

<p><em>Images: Courtesy Shoulin Animation &amp; Getty </em></p> <p>Scientists are showing off a perfectly preserved dinosaur embryo fossil that was preparing to hatch from its egg, much like a modern-day chicken.</p> <p>The embryo fossil, nicknamed “Baby Yingliang,” was discovered in Ganzhou, Jiangxi Province in southern China, and is believed to be at least 66 million years old.</p> <p>Researcher Dr. Fion Waisum Ma told the AFP News Agency that this discovery is “the best dinosaur embryo ever found in history.”</p> <p>According to a study, researchers at a Chinese mining company, Yinagliang Group, found the egg fossil more than 20 years ago, but put it in storage with other fossils for 10 years.</p> <p><img style="width: 500px; height: 281.25px;" src="https://oversixtydev.blob.core.windows.net/media/7846550/new-project.jpg" alt="" data-udi="umb://media/8b66ef36cdec4b21b7bfdff89ef98730" /></p> <p>When construction began on the company’s natural history museum, the fossil storage was sorted, and museum staff pulled the dinosaur eggs from the collection for closer examination. That’s when they noticed some bones on the broken cross section of one of the eggs.</p> <p>Researchers say the egg belonged to a toothless theropod dinosaur, or oviraptorosaur. Ma and fellow colleagues found Baby Yingliang’s head below its body, with its feet on either side and back curled. This posture is familiar in modern birds but not previously seen in dinosaurs.</p> <p>Researchers believe the animal was on the verge of hatching, but it was likely preserved when it was buried by a sudden mudslide.</p> <p>Oviraptorosaurs, one of the closest relatives to the bird, evolved earlier from small, feathered dinosaurs. This group of dinosaurs was still blossoming and diversifying during the last few million years before an asteroid struck Earth about 66 million years ago, wiping out the dinosaurs.</p> <p>The baby dino measures about 27 centimetres long and is currently on display at the Yinglliang Stone Natural History Museum. Most likely a herbivore, it would have grown to be about three metres long if it lived to adulthood.</p> <p>“We were surprised to see this embryo beautifully preserved inside a dinosaur egg, lying in a bird-like posture. This posture had not been recognized in non-avian dinosaurs before,” Waisum Maof of the University of Birmingham, told CBS News.</p> <p>Despite fossilised dinosaur eggs having been found during the last 100 years, a well-preserved embryo is extremely rare, the researchers said in their study. Paleontologists have found them over the years only six times.</p>

International Travel

Placeholder Content Image

China's failed gene edited baby experiment proves we're not ready for human embryo modification

<p>More than a year ago, the world was shocked by Chinese biophysicist He Jiankui’s attempt to use CRISPR technology to modify human embryos and make them resistant to HIV, which led to the birth of twins Lulu and Nana.</p> <p>Now, crucial details have been revealed in a recent <a href="https://www.technologyreview.com/s/614764/chinas-crispr-babies-read-exclusive-excerpts-he-jiankui-paper/">release of excerpts</a> from the study, which have triggered a series of concerns about how Lulu and Nana’s genome was modified.</p> <p><strong>How CRISPR works</strong></p> <p>CRISPR is a technique that allows scientists to make precise edits to any DNA by altering its sequence.</p> <p>When using CRISPR, you may be trying to “knock out” a gene by rendering it inactive, or trying to achieve specific modifications, such as introducing or removing a desired piece of DNA.</p> <p>Gene editing with the CRISPR system relies on an association of two molecules. One is a protein, called Cas9, that is responsible for “cutting” the DNA. The other molecule is a short RNA (ribonucleic acid) molecule which works as a “guide” that brings Cas9 to the position where it is supposed to cut.</p> <p>The system also needs help from the cells being edited. DNA damage is frequent, so cells regularly have to repair the DNA lesions. The associated repair mechanisms are what introduce the deletions, insertions or modifications when performing gene editing.</p> <p><strong>How the genomes of Lulu and Nana were modified</strong></p> <p>He Jiankui and his colleagues were targeting a gene called CCR5, which is necessary for the HIV virus to enter into white blood cells (<a href="https://www.medicalnewstoday.com/articles/320987.php">lymphocytes</a>) and infect our body.</p> <p>One variant of CCR5, called CCR5 Δ32, is missing a particular string of 32 “letters” of DNA code. This variant naturally occurs in the human population, and results in a high level of resistance to the most common type of HIV virus.</p> <p>The team wanted to recreate this mutation using CRISPR on human embryos, in a bid to render them resistant to HIV infection. But this did not go as planned, and there are several ways they may have failed.</p> <p>First, despite claiming in the abstract of their unpublished article that they reproduced the human CCR5 mutation, in reality the team tried to modify CCR5 <em>close</em> to the Δ32 mutation.</p> <p>As a result, they generated different mutations, of which the effects are unknown. It may or may not confer HIV resistance, and may or may not have other consequences.</p> <p>Worryingly, they did not test any of this, and went ahead with implanting the embryos. This is unjustifiable.</p> <p><strong>The mosaic effect</strong></p> <p>A second source of errors could have been that the editing was not perfectly efficient. This means that not all cells in the embryos were necessarily edited.</p> <p>When an organism has a mixture of edited and unedited cells, it is called a “mosaic”. While the available data are still limited, it seems that both Lulu and Nana are mosaic.</p> <p>This makes it even less likely that the gene-edited babies would be resistant to HIV infection. The risk of mosaicism should have been another reason not to implant the embryos.</p> <p>Moreover, editing can have unintended impacts elsewhere in the genome.</p> <p>When designing a CRISPR experiment, you choose the “guide” RNA so that its sequence is unique to the gene you are targeting. However, “off-target” cuts can still happen elsewhere in the genome, at places that have a similar sequence.</p> <p>He Jiankui and his team tested cells from the edited embryos, and reported only one off-target modification. However, that testing required sampling the cells, which were therefore no longer part of the embryos - which continued developing.</p> <p>Thus, the remaining cells in the embryos had not been tested, and may have had different off-target modifications.</p> <p>This is not the team’s fault, as there will always be limitations in detecting off-target and mosaicism, and we can only get a partial picture.</p> <p>However, that partial picture should have made them pause.</p> <p><strong>A bad idea to begin</strong></p> <p>Above, we have described several risks associated with the modifications made on the embryos, which could be passed on to future generations.</p> <p>Embryo editing is only ethically justifiable in cases where the benefits clearly outweigh the risks.</p> <p>Technical issues aside, the researchers did not even address an unmet medical need.</p> <p>While the twins’ father was HIV-positive, there is already a well-established way to prevent an HIV-positive father from infecting embryos. This “<a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4779710/">sperm washing</a>” method was actually used by the team.</p> <p>The only benefit of the attempted gene modification, if proven, would have been a reduced risk of HIV infection for the twins later in life.</p> <p>But there are safer existing ways to control the risk of infection, such as condoms and mandatory testing of blood donations.</p> <p><strong>Implications for gene editing as a field</strong></p> <p>Gene editing has endless applications. It can be used to <a href="https://www.nature.com/articles/d41586-019-02770-7">make plants such as the Cavendish banana more resistant to devastating diseases</a>. It can play an important role in the adaptation to climate change.</p> <p>In health, we are already seeing <a href="https://www.npr.org/sections/health-shots/2019/11/19/780510277/gene-edited-supercells-make-progress-in-fight-against-sickle-cell-disease">promising results</a> with the editing of somatic cells (that is, non-heritable modifications of the patient’s own cells) in beta thalassemia and sickle cell disease.</p> <p>However, we are just not ready for human embryo editing. Our techniques are not mature enough, and no case has been made for a widespread need that other techniques, such as preimplantation genetic testing, could not address.</p> <p>There is also much work still needed on governance. There have been individual calls for a moratorium on embryo editing, and expert panels from the <a href="https://www.nature.com/articles/d41586-019-00942-z">World Health Organisation</a> to <a href="https://en.unesco.org/news/unesco-panel-experts-calls-ban-editing-human-dna-avoid-unethical-tampering-hereditary-traits">UNESCO</a>.</p> <p>Yet, no consensus has emerged.</p> <p>It is important these discussions move <a href="https://www.nature.com/articles/d41586-019-03525-0">in unison</a> to a second phase, where other stakeholders, such as patient groups, are more broadly consulted (and informed). Engagement with the public is also crucial.</p> <p><em>Correction: this article originally described RNA (ribonucleic acid) as a protein, rather than a molecule.<!-- Below is The Conversation's page counter tag. Please DO NOT REMOVE. --><img style="border: none !important; box-shadow: none !important; margin: 0 !important; max-height: 1px !important; max-width: 1px !important; min-height: 1px !important; min-width: 1px !important; opacity: 0 !important; outline: none !important; padding: 0 !important; text-shadow: none !important;" src="https://counter.theconversation.com/content/128454/count.gif?distributor=republish-lightbox-basic" alt="The Conversation" width="1" height="1" /><!-- End of code. If you don't see any code above, please get new code from the Advanced tab after you click the republish button. The page counter does not collect any personal data. More info: http://theconversation.com/republishing-guidelines --></em></p> <p><em><a href="https://theconversation.com/profiles/dimitri-perrin-392467">Dimitri Perrin</a>, Senior Lecturer, <a href="http://theconversation.com/institutions/queensland-university-of-technology-847">Queensland University of Technology</a> and <a href="https://theconversation.com/profiles/gaetan-burgio-202386">Gaetan Burgio</a>, Geneticist and Group Leader, The John Curtin School of Medical Research, <a href="http://theconversation.com/institutions/australian-national-university-877">Australian National University</a></em></p> <p><em>This article is republished from <a href="http://theconversation.com">The Conversation</a> under a Creative Commons license. Read the <a href="https://theconversation.com/chinas-failed-gene-edited-baby-experiment-proves-were-not-ready-for-human-embryo-modification-128454">original article</a>.</em></p>

Technology

Placeholder Content Image

Baby girl born from embryo frozen 24 years ago

<p>A 26-year-old American woman has given birth to a baby that grew from an embryo frozen 24 years earlier.</p> <p>Tina Gibson, of east Tennessee, was 25 when she gave birth to Emma Gibson in November with husband Benjamin.</p> <p>Emma grew from an embryo that was originally frozen on 14 October 1992.</p> <p>“If the baby was born when it was supposed to born, we could have been best friends,” Tina Gibson <span style="text-decoration: underline;"><strong><a href="https://www.nbcnews.com/health/health-news/couple-has-baby-24-year-old-frozen-embryo-n831331">told NBC News</a>.</strong></span></p> <p>"Emma is such a sweet miracle," her father, Benjamin Gibson, said in a <span style="text-decoration: underline;"><strong><a href="http://www.standardnewswire.com/news/1848813372.html" target="_blank">news release</a>.</strong></span> "I think she looks pretty perfect to have been frozen all those years ago."</p> <p>The embryo was transferred into Tina’s uterus by the National Embryo Donation Center, a faith-based organization in Tennessee.</p> <p>“We’re just so thankful and blessed. She’s a precious Christmas gift from the lord,” Gibson said, <span style="text-decoration: underline;"><strong><a href="http://www.cnn.com/2017/12/19/health/snowbaby-oldest-embryo-bn/index.html">according to CNN</a></strong></span>. “We’re just so grateful.”</p> <p>After a couple goes through IVF treatment there are sometimes leftover embryos, which are frozen for potential later use.</p> <p>The National Embryo Donation Center encourages people to donate those embryos to other couples who are unable to conceive. </p> <p>The NEDC’s Dr Jeffrey Keenan, who oversaw the embryo transfer, said it may be a record length between the donating of an embryo and the delivery of a child.</p> <p> “We had our medical library, which is very good at finding things, look to see if they could find anything older than that and they could not,” Keenan told NBC News.</p> <p>“But it is kind of neat that this embryo was conceived just a year or so before the mother was.”</p> <p>The organisation hopes couples who have leftover embryos will consider this as an option for those who want to become parents. </p>

Family & Pets

Our Partners