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Monday, May 31, 2021

Genetic Chimeras: From Myth to Real Life


 Figure 1: Depiction of a mythical Chimera (Greek Mythology)

Creation

The Scientist recently reported that scientists are creating human-animal chimeras in various experiments. Humans have been fascinated by such creations since ancient times. In general, a chimera is an organism composed of cells that originate from at least two different species. Typically they're made by injecting stem cells from one species into a developing fetus or embryo of a different species. Each chimera cell contains the genetic material of either one parent species or the other, but not both.

Chimeras aren't the same as hybrids, which are bred from two parents of different species (e.g., a donkey and a horse can mate to make a mule), and therefore contain both species' genes in all cells. Hybrids can be multivariate and may contain a varying percentage of genetic material from both species in their cells. Hybrids can often come about without any human intervention, whereas chimeras require it.

Chimeras are also different from the condition of chimerism that is found in humans and other animals. Chimerism refers to an individual with two complete genomes from the same species/parents. This occurs spontaneously, most often when a person absorbs their twin while in utero. Chimerism is incredibly rare, as only around 100 cases have been recorded in all of modern medical literature.

Figure 2: Diagram of the creation of a chimeric organism using induced pluripotent stem cells, or iPSCs. Source

Although people have talked about chimeras for a long time, the technologies required are still in their infancy. In the 1960s, researchers tried unsuccessfully to create a quail-chicken chimera. This research eventually found success in 1973 with the creating of a mouse-rat chimera, although many of those created did not live to adulthood. The first chimera that fully survived to adulthood was a goat-sheep chimera created in 1984 (see Figure 3). Despite the strides that chimera creation methods have made, we have still only scratched the surface of the potential uses of chimeras for humans.

Figure 3:  A picture of one of the earliest successful chimeras, a goat-sheep chimera

Uses for Chimeras

Many if not all of the projected uses for chimeras are found in medical fields. For example, in various current studies, scientists are investigating the transplant of functioning human organs from chimeras.

Other chimera-focused medical studies include pig-human, sheep-human, rabbit-human, and monkey-human chimeras, and their applications in organ transplant, stem cell research, and the study of neurological diseases.  

Figure 4: Diagram of how organ transplant between humans and livestock may be undertaken. Source

Opposition to Creating Chimeras 

With all of the scientific efforts involving human chimeras, it was inevitable that moral dilemmas involving animal rights and concerns about the health and well-being of animals involved would come forward. The Guidelines of Human Embryonic Stem Cell Research, published by the National Academies, outlawed the breeding of chimeras in the United States, principally because it could create a human zygote if two chimeras with human gametes were to mate. Currently, there is no international consensus over these or any guidelines.

Many people also object to the use of human embryonic cells to help create chimeras. Multiple studies have specifically involved the growth of human brain cells inside of a chimera, for research or organ transplant. But if those animals eventually have a completely human brain, can they be counted as human? (Source)

My Takeaways

Just like any new and experimental technology, chimera creation and testing have many potential positives and pitfalls. It could be used to save many lives, but it could also establish dangerous moral precedents that we as a species may regret pursuing. Chimeras are in the realm of what scientists considered impossible 75 years ago, and show the massive progression of human science.

In my opinion, chimera creation is a technology that we as a species must be incredibly careful with. It is not enough that there are guidelines set in the United States. While many other countries also have guidelines, not all do, and some other countries' restrictions may not be as strict as those here. Until there are unified guidelines adopted by all countries I will remain concerned.

I became interested in this topic from reading some of the numerous articles about chimera studies and research published by news organizations such as The Scientist, the BBC, and CNN in recent years about chimera studies and research. I will continue to track this topic.

Friday, May 28, 2021

Stem cells; the future of medicine

 You may have heard about stem cells. People are saying they are the future of medical research, but you may be asking yourself "What are stem cells and what can they be used for?". Cells are the smallest units or building blocks that make up living things.  All cells in a human body contain identical genetic information but different types of cells carry out different functions. This is due to differentiation. Stem cells are cells that have the ability to specialize into any type of cell. Stem cells are found mostly in bone marrow but can also be found in umbilical cords, amniotic fluid and organs such as the skin, heart and liver. Stem cells are cells that have not yet differentiated. Because of this, through the artificial introduction of different transcription factors stem cells can be differentiated into any type of cell. This is what makes them special. You can learn more about stem cells here

The different differentiation potentials of a stem cell

Stem cells' ability to differentiate allows them to specialize into any type of cell. This differentiation ability can be used to treat illnesses such as lymphoma, leukemia and aplastic anemia. Bone marrow is tissue found inside bones that is responsible for creating blood cells. There are two types of bone marrow/ stem cell transplants, autologous and allogenic. Autologous transplants are when patients receive a donation of their own stem cells that were harvested before chemotherapy. Allogenic transplants are when patients receive a donation from a donor. Bone marrow transplants are used to treat patients who lack healthy bone marrow and therefore cannot produce healthy blood cells. You can learn more about this here



Stem cells role in bone marrow transplants


Stem cells are also being developed for use in regenerative therapy. Their ability to differentiate into different cells allows them to be used to replace damaged cells in organs. Mesenchymal stem cells are at the center of this research due to their ability to differentiate into specialized cells found in different organs such as the heart, the liver, the eye and more. Mesenchymal stem cells are stem cells that are found in bone marrow, amniotic fluid, and fat tissue that can differentiate into many different types of cells.  Mesenchymal stem cells are also favorable because they are immunoprivileged which means they are able to be transplanted with little to no risk of rejection. Stem cells are harvested either by a procedure where a needle is used to collect stem cells from the bone marrow or by giving a donor medication to increase stem cell production then drawing blood and separating the stem cells. Then the stem cells are transplanted to the organ where they will differentiate into new working cells to replace damaged ones. you can read more about how transplants are carried out here and the role of stem cells in regeneration here.

The different uses for mesenchymal stem cells

There has also been a lot of controversy about the use of stem cells in research due to the fact that one source of stem cells is embryos. However most stem cells used in treatment and research are not embryonic stem cells and the ones that are are mostly from embryos leftover from IVF treatments that would have been destroyed otherwise where the donors have given informed consent for their embryos to be used. You can read more about the ethical concerns about embryonic stem cells here. Furthermore, the scientific developments that have come from fetal tissue, which is different from embryonic stem cells, are immense. They include the development of certain vaccines and treatments for maternal hypertension, heart disease, and diabetes.

CRISPR: The Genetic Editing Technique That May Change life As We Know It

Hi Noah! What you have is good so far (there are just some minor grammatical errors for the most part) but there is not enough content here. Another student wrote about CRISPR and the post was much longer. Her focus was on the ethics and although it's fine that you mention the ethics, I would like you to provide more content about what diseases are currently being treated or have been treated w/ CRISPR as well as how else it's being used medically and in research. You need at least two more paragraphs. After making those edits (be sure there are no sentence fragments), you can publish.


Intro on CRISPR 

CRISPR is short for Clustered Regularly Interspaced Short Palindromic Repeat., which refers to the regions in bacteria genomes that assist in defending against viruses.CRISPR genomes are extremely important in the immune systems of bacteria and other microorganisms. CRISPR immune systems fight viruses by interpreting DNA from that virus (via spacers), then transcribing CRISPR RNA which is used to guide molecular machinery to fight the viruses. CRISPR is basically the ultimate virus-fighting machine. 

A Figure showing how the CRISPR immune system works. Source


The Importance of CRISPR


Even though CRISPR immune systems already are viral superheroes, there are many more incredible applications that CRISPRs can be used for in today's world. Scientists are utilizing CRISPR techniques to make genetic changes in organisms, even experimenting with human cells. They do this by inserting RNA molecules that match the DNA sequence of a specific cell. Then, similarly to when a virus attacks a cell, the RNA guides molecular machinery that can be used to change the sequence of a gene. 


There are many different applications of the CRISPR gene-editing technique. It can be used to help prevent certain viruses or pesticides from damaging food, but the most important application of this new technology is in medicine. Scientists can apply this technique to treat genetic diseases. Not only heritable diseases but infectious diseases too. The possibilities are endless. 


Science & Tech Spotlight: CRISPR Gene Editing

 This illustration shows the possibilities and challenges of this new technique. Source


CRISPR Concerns


Since it is a relatively new technology, there are very many concerns surrounding it. Some concerns include regulatory issues with crops, while others pertain to the general safety of this technique as there is still a lot more research to be done about it. However, the most talked-about issue regarding CRISPR technology is the ethical concerns. It is okay for scientists to edit sperm cells for embryos to create genetically engineered humans with “special” characteristics and how genetic modification of humans could affect future generations. In 2019, a scientist announced that two twin girls have been born with edited genomes. This caused public outrage and more debates over the ethics of gene editing. Despite the concerns, CRISPR techniques are still being researched and will be incredibly useful to the health of future generations. 

More on the Medical Side of CRISPR

When the CRISPR technique became public, researchers and scientists everywhere began to ponder as to the certain medical diseases that can be treated with the CRISPR techniques. With the global pandemic taking place, there have also been a scientist wondering if this can be a future quick fix to many viral diseases. In the article linked below, there is a description of the 8 possible diseases that could be cured with CRISPR treatments. While this is all still in the works, the article also explains what testing and research has been done to target each disease using this new technology. 

Scientists are also using CRISPR technology in many different medical fields. Some scientists are experimenting in creating an STD prevention genome using CRISPR technology. This is Targeted specifically towards an ongoing fight against HIV. Another use of this technology is to create resistance to malaria in foreign countries. Overall, the CRISPR techniques are amazing and will hopefully help us attack diseases and better human life.