top of page

Treasured Hands Inc Group

Public·12 members
Eldar Aksenov
Eldar Aksenov

[S1E4] Just Let Go ((EXCLUSIVE))



Sonix is an automated transcription service. We transcribe audio and video files for storytellers all over the world. We are not associated with the In the Dark Podcast. Making transcripts available for listeners and those that are hearing-impaired is just something we like to do. If you are interested in automated transcription, click here for 30 free minutes.




[S1E4] Just Let Go


Download: https://www.google.com/url?q=https%3A%2F%2Ftweeat.com%2F2uiG78&sa=D&sntz=1&usg=AOvVaw1984pPnSWgYP25RBHseHNl



The episode starts off simply, with Blythe just walking Zoe down the sidewalk. Zoe reveals to the audience that she has a sister named Gail, and is excited about getting to introduce her to Blythe later in the day. La de da, polite chatter, until Zoe notices Gail trapped inside Largest Ever Pet Shop daycare, looking very depressed. Dun dun dun!


Zoe confirms that it's Gail from that fabulous collar, and the two notice something else; THEY HAVE A FREAKING ROBOT SECURITY SYSTEM. Not just cameras or anything. I'm talking a mobile, vaguely humanoid robot that talks. Why? Why is that necessary? Couldn't such a discovery be used for something more important? No matter, Blythe tries to go into the store and inform them of what is clearly an obvious mix up. Suddenly, the Biskits.


This isn't too much of a setback for their plans, though, because Pepper and Vinnie were only needed for something they didn't end up having to do. Russell goes through the plan again, and then Minka pulls a Leeroy Jenkins on them and rushes in. The Biskits spot her through the security camera, and after mentally asking themselves what the flying feather just happened, they tell Monban to capture the monkey in aisle 8. No wait, aisle 7, no wait, aisle 9, no wait, aisle 10? Aisle 11? Minka is eventually cornered when she runs to the daycamp center and is caged up. This basically sums her up except for being an artist, yeah.


Russell comes up with a Plan C now. If Penny Ling just reverses the polarity of the neutron flow cash register, that should send a signal at the right frequency to shut off Monban and I didn't pay attention to the rest because I'm too busy being amazed that they made a Doctor Who reference. Blythe says she has something simpler in mind. She walks in and distracts Monban while Zoe sneaks by. Monban runs down the hall while shouting "Stop! Resistance is futile useless!". Q and Star Wars ending in The Return Of Harmony and this? Something tells me that Mitch Larson is a science fiction fan. Zoe gets there and nearly busts them out... but her favorite song comes on again, and she can't resist the music. Chekhov's Gun No. 1, checked off. The Biskits find Blythe, who receives a double ban from the Largest Ever Pet Shop.


Monban's battery runs low, and while he's charging up, Penny Ling goes in with her ribbons. She gets tangled up with them and some boxes, but she figures that Monban is off, and therefore there's nothing to worry about. Her reduced speed proves to be her downfall, and Monban finishes charging just in time to stop her from letting the pets go. Well shit. Now we are down to Blythe, Russell, and Sunil.


I wasn't a big fan of Dragonshy, but I imagine this is what the fans of that episode saw when Fluttershy stood up to the dragon. I promised that I would explain why everybody loves Sunil so much, and this is why. His transformation from coward to warrior is just awesome, and the amazing backing music doesn't hurt matters. He murders the pet toys and food and then just tops it off by hypnotizing the Biskits in a flash and throwing the headphones on Monban like a boss.


These are clones. A clone is a living thing, genetically identical to another living thing. You and I are one of a kind. But what if you were not? What if we could make a duplicate of you? Genetically exact. Should we? People fear genetically engineered clones. What an individual still be individual. See it may be possible to use the same techniques that we use to clone a new person to instead rebuild or repair organs or even cure genetic diseases. The things we're talking about are microscopic. But the possibilities are far reaching. Should we pursue cloning? What we're going to look at the science and then we can each decide for ourselves. The eyes are not. These are clones. Each of these grapevines is just like all the other vines. They were all grown from cuttings of the same plant. In fact, our word clone comes from the Greek word for twig. See, clones are not that unusual. They're offspring produced without sex. These two plants are genetically identical and asexually reproduced. They both came from a single parent. And they both have the same DNA. And when these individuals were created, there was no help from two hours or the birds and the bees, no pollen was exchanged. There was no sex. I'm pregnant. I'm going to be a you're not a father. What? Who is. Oh, Gilliam. I am the father. But you are the mother. I am the mother and the father. That explains why you never let me turn on the lights. No. Listen, like the Grapevine I have discovered the beauty of age sexual reproduction. I didn't know grapes could be so nasty. You hear that. I have grown myself. So the baby will be all of me and none of you. And this baby, it will be just like you. Not necessarily. She will look like me, but she might not be like me. In that case. Tell her to call me in about. 18 years. Yeah, out. Get out of my sight. You make me sick. Ah, humans. Now, we can't reproduce asexually. We just cloning ourselves like grapevines. Oh no. We have to have sex. And for many, that's not a problem. That couple has started on the process of sexual reproduction, where half of the genetic information comes from the woman and half comes from the men. But we're talking about cloning. Asexual reproduction, where all of the DNA comes from a single parent. All of the cells in your body that are not sperms or eggs are called somatic cells and almost every somatic cell carries a complete copy of an organism's DNA. So to clone an animal like Dolly the sheep, scientists start with an egg. Then using the tiniest of glass pipettes, they pull the nucleus of that egg. Out. And then they get the DNA from another somatic cell, or they take a wholesale DNA in all and poke it back into that egg. Now this is called somatic cell nuclear transfer. It's cloning. Then scientists give this egg a tiny jolt of electricity or just the right chemical mix to get it to start growing to start dividing. Then they put it back into the womb of a sheep, and if nothing goes wrong in a few months, you get a lamb. Dolly the sheep was born on the 277th trying. That's after 276 failures. Cloning is a tricky business. Now, if we have this much trouble with farm animals, are we really ready to try it with humans? Now it's time for opinions now with your host Chris David. Tonight, what would human clones be like? Biologist doctor albie, what do you think? It's very difficult to say. Yes. Now. As a scientist, I don't really guess about it. This guy, genetics expert, doctor Sandra Davis, what would human clones be like? Well, we're not really sure. Come on, cut the bull doctor. Well, if you'd like me to speculate. Yes. Speculate. Wildly. Now. I won't speculate wildly, but a reasoned hypothesis is that we could all end up with that loss of a certain spark that makes us individuals. You're saying that we would all be sheep headed zombies. Not necessarily. Jack booted stormtroopers engineered to be perfect soldiers as part of the government's plan to make us all prisoners to its will excuse me. I didn't get to make my comment. Yeah, nobody cares. Biologist boy. But as a scientist, I thought you'd want my expert opinion. I'm outta here. Proteins and sea squirts and human embryos are the same proteins that are causing embryonic development. So they're the same genes as people. Right. A human starts as one cell, a C squirt starts as one cell. But it's the way the genes are turned on and off that decides what it's going to finally look like. So you use these animals to study cloning. Great. We use into study how genes are turned on and off during development. So most of your cells right now, the DNA is off, which means it's not making protein. They might have been used before to make an ear, but now that you have an ear. Those cells are only used for specific functions. But when you're being born, when you're a single cell. The egg starts as a single cell, so that first single cell has to somehow turn on and off all the genes necessary to make that adult organism. Now, how does that happen? The egg actually puts proteins in the cytoplasm that tells the nucleus where certain things are supposed to be made. So those transcription factors proteins. Protein CS transcription factors will go into the nucleus at certain times and then turn certain genes on and off. And each animal has the same set of genes turning things on and off, but it's how and when you turn different genes on and off, that makes different adults. What you do in cloning is you take this nucleus out of there and you put in a nucleus from an adult and that's the difficult part. It's getting that nucleus from an adult to go through this whole process of making an embryo. The reasons reproductive cloning doesn't work very well is because you have to take the old nucleus and you have to make it think that it's a young nucleus. You have to make it think it's a nucleus that's in an egg. This is a difficult process and these nuclei are old nuclei, so a nucleus in your, say, skin might have lived so far for a number of years, maybe 40 some years. And so you have to take that old nucleus and try to make it young again. And we're not sure how to do that. That's one of the most difficult things about reproductive cloning. It's a very low success rate, maybe one to 2%. If you try to clone yourself. Is that why Dolly was such a big deal? Well, Dolly was a big deal because she was cloned. She also died at the age of 7, which is about half as old as a regular sheep would live. And so there's some idea that the nucleus was too old, and that's why she died a premature age is because even though the nucleus was tricked into thinking it was young again, it really wasn't that young again. And so she died. The same area in Tommy reproductive cloning of human beings is a bad idea. A few clones had survived, could have severe health problems. Gosh, mister Sanders, that sounds terrible. But mister Sanders, wouldn't you like to be called? Now, Tommy, would you really want to see another balding middle aged science teacher who lives with his mother walking around? That's my little pony joke. Oh. Good one, mister Sanders. Do you still live with your mother, mister Sanders? No, Tommy, what I'm saying is that cloning for reproduction is fraught with peril. You know, mister Sanders, you are losing your hair. Now, children, let's focus on cloney and not me, okay? Have you ever kissed a girl, misses Sanders? Maybe we should watch another segment of the eyes of Nye science program. Yes, Mary. Perhaps we should. Are you crying, mister Sanders? No, Tommy, I just got something in my eye. So what's the controversy then about reproductive crime? Well, I think there's really two controversies. The first controversy is where do you get the eggs? So people are worried that they'll be some sort of black market for human eggs that young girls who otherwise might not give their eggs away will be induced to do that for money. So the source wears a source of eggs is one problem and then the second one I think is the embryos themselves. When you understand human development, you'll understand that you can not make a baby from those embryos unless they're implanted into our uterus. So as long as the embryo is kept in culture and kept outside of the mother, it will not make another human being. Is there a place to draw the line? For the society for developmental biology, as scientists, we've come up with the rule that we're for therapeutic cloning and not for reproductive cloning. When it comes to the technology of cloning, the train is pretty much left the station. See, once we perform somatic cell nuclear transfer, we get an embryo, and a lot of fetus, an embryo, cells that are dividing. Now there's two choices as to how we use that embryo. We can go this way. What we call reproductive cloning, make a new cow or a sheep, or theoretically, even a person, but we don't have to go that way. If we don't implement the embryo into a womb, just let it grow, we can instead go this way. And this is therapeutic one. And the cells grow and divide is what we call stem cells. A stem cells can become any type of cell. And here's the thing, the procedure for reproductive cloning and therapeutic cloning is exactly the same up to this point. Up to this point. This fork in the row. If we go this way, we would get new people. If we go this way, we would get new cells. Which way do you want to go? Bill of cloning is so risky and dangerous. Why bother? Well, Bill, if we were to perform a somatic cell nuclear transfer and fuse it so that it started to grow, we'd get an embryo. We don't get a person. No, an embryo, a ball of cells that's growing and dividing. So we couldn't be talking like this. No, no, this is an old TV trick. At 5 days along, an embryo has about 200 cells, and they're undifferentiated. Undifferentiated? Yes, they haven't started to become all the different cells of your body, like your skin cells, your bone cells, and your brain cells. Their stem cells, and they have astonishing promise. But if you had to choose between, say, me and a bunch of stem cells, which one would you pick? Okay, well, here's the fun stuff. So these are colonies of stem cells. Right, these are human embryonic stem cells. Each one of these colonies derived from one single cell. One of these back here? That's right. That has divided and divided and divided and divided eventually forming now a few thousand cells in a free floating cluster so that we have millions and millions of cells all exactly the same. And then the next step is to change them first into brain and then into a subtype of brain that we'd like for repair. So this is the center of one of those large clusters that is now stuck down. And as we move away, you can see very small little cells that all look the same, but then as we move further away, now we start to see them differentiate into these long mature cells with long processes. So what do we do with these cells? Spin them down, soles to concentrate them and squirt them into a spinal cord injury in a rat. So here's an animal that received an injury with no transplant. So this animal has not been transplanted, and you can see that he's not standing and just sort of drags his hind limbs around without any coordinated locomotion front to back. Can't move his back legs. Very little. It's not a complete injury. This models human spinal cord injuries that are the most common type of them. Those sustained like a car accident or diving accident sporting called a contusion injury. So that's what we're trying to treat. It's a pretty severe injury. So you injected this rat with the human embryonic stem cells. That's right, that we first tricked to become brain committed and then to a subtype of brain that we know to support repair. Let me just show you what that looks like. This is a nice shot here because we can see that the legs are moving in a coordinated fashion side to side. So it's not only a matter of controlling one side of his body, can actually control both. And tail is up, so he's got full control of his back muscles. And one thing you can't see in this video is that these animals regained control of bladder and bowel function of earlier than the non transplanted animals. That's the number one concern of people in wheelchairs. But if we take an animal with a similar injury, only two weeks after transplants, but you can see he's supporting his weight and standing, and you can see he actually takes some steps. Yeah, he's doing well. So what's happening inside the rents? Well, what's happening is that the cells that we put in are integrating into the spinal cord and the spinal cord itself is growing through the injury and transplant site up above the injury site. So it's anatomical evidence for repair. So how long did this take? This took about ten weeks. So this works. It looks like it's working out. Say this is strong preliminary evidence that human embryonic stem cells have a real beneficial future. Would you say you're in favor of therapeutic line? Absolutely. I think therapeutic cloning could be to brain trauma and disease, treatment, what the jet engine was to the airline industry. Good evening, my guest is congressman Peter Newton. Congressman, what do you think about the controversial procedure of using embryonic stem cells in research? I have said many times that we really need to study the subject more and not rush into a decision. But many people say that a tiny embryo, even one consisting of just a few undifferentiated cells should be given full human dignity and worth. Well, absolutely. It is outrageous. What is being done? We need to stop this stem cell madness. No. However, some studies show that up to half of all people could benefit from stem cell research. Is that the half that votes because if so, I say let's stop this foolishness and fully fund this research right now. I think putting tastes good. You know, I have always supported putting even when it was politically unpopular to do so. I give up. Is it okay to take a woman's egg? And use it to grow stem cells. Is that okay? No, not to me. I don't think so. I think everything should be able to live. At that stage of its development, it doesn't really have it's just kind of like any other cell. When it has the potential to grow into a human, but it's not necessarily a human. I would say yes. It certainly is okay, because after all, I mean, if she doesn't give up the egg, and if it's not fertilized, she's going to expel it anyhow. Look at a woman, how many eggs she passes a year. You know, it's an egg. You know, you got a lot of them. I'm sure I could start one. Here in the United States, the debate about embryonic stem cell research rages on. It is a debate about life. On one side shouldn't we use this technology that could improve the lives of millions of people who are already here, people have been struck with disease or injury. On the other side, the question is, when does life begin? Some believe life begins the moment the first cell divides. So if the Petri dish holds living cells, is it morally acceptable to redirect those cells and transform them into something they wouldn't otherwise become? Then there are concerns about the industrialization of life. Should human embryos be declared inventions that you could patent, that's what we have to figure out. But how do we pursue a thoughtful discussion on stem cell research? Can we find a way to make our trains meet? Bioethicist, bioethicists, bioethicists. We're all ethics experts because we all have to make decisions about what's right and wrong. And it's not fair to ask me or any one person. What's the right place to draw the line? It's a question that we all have to answer, collectively, socially, because it's an issue of social policy. We have to decide at what point do we think it's acceptable to use human embryos and potentially pass human embryos and we have to answer is an embryo, a human embryo in terms of its moral status, more like the cells you can scrape out of your cheek or more like the person who's sitting before you today. You or I. And I think it's in between. And the question is, I think not whether there's some moral status of human embryos, because I think most people think there is some moral status. But it's not full human being personhood status. And it's not mere tissue. It's in between those two. And the question is, what's the moral benefit we can get fro


About

Welcome to the group! You can connect with other members, ge...

Members

bottom of page