Term Paper on "Embryonic Stem Cell Research in November 1998"
Term Paper 6 pages (1529 words) Sources: 1+
[EXCERPT] . . . .
Embryonic Stem Cell ResearchIn November 1998, two research groups independently announced that they had isolated human stem cells from embryonic tissues, had cultivated the cells, and shown these cells could develop into all three basic layers of cells in the human embryo (Lysaught 1999). Because these cells could potentially develop into nearly every type of human cell and tissue, they held great promise for applications in medicine and human development (Lysaught 1999).
Upon announcement of the news, Harold Varmus, director of the National Institutes of Health, was quoted as saying that human embryonic stem cell research "had the potential to revolutionize the practice of medicine and improve the quality and length of life" (Lysaught 1999). Concerns arose regarding the fact that the techniques by which stem cells were derived involved the destruction of human embryos, thus depriving them of their potential to develop into human beings (Lysaught 1999). Another concern was that some scientists might "tinker" with human life through some "grand" experiment in eugenics (Lysaught 1999).
Dating back to at least 1981, embryonic stem cells were first successfully cultured from mouse embryos, followed by the isolation of embryonic stem cells from various animals, including sheep, hamsters, pigs, cows, rabbits, mink, rhesus monkeys, and marmosets (Lysaught 1999). However, culturing human embryonic stem cells proved more difficult, for once isolated, they refused to stay undifferentiated, "seemingly driven to spontaneously differentiate and form primitive structures (Lysaught 1999). The first publicly acknowledged, yet unsuccessful, attempt to isolate and cultu
download full paper ⤓
First, Gearhart's group isolated what are called primordial germ (PG) or embryonic germ (EG) cells, which are precursors of sperm and egg cells. Second, the cells were obtained not from embryos made in vitro but from aborted fetuses that were 5 -- 9 weeks old.
Tests showed that these cells had a number of characteristics typical of stem cells and could further develop into the three embryonic germ layers (Lysaught 1999).
These reports sparked much excitement because researchers could now design experiments to determine how human embryonic cells differentiate into various types of tissues, leading to the development of the human body, and moreover, because of the capability of these cells, a wide range of clinical applications were predicted (Lysaught 1999). Embryonic stem cells can be coaxed to differentiate into nerve or brain cells that could then be used to treat neurological disorders including Alzheimer's and Parkinson's diseases (Lysaught 1999). Moreover, if embryonic stem cells were transformed into heart muscle cells, they could be used to replace damaged tissue in the hearts of those who have suffered heart attacks or congestive heart failure (Lysaught 1999). Or they could be used to produce pancreatic islet cells in culture which could then be injected into the pancreas of a diabetic to manufacture insulin, thus reducing or eliminating the need for daily injections (Lysaught 1999). Furthermore, cell lines derived from embryonic stem cells could be used to grow entire organs for replacement, while other cell line could be used as human tissue banks against which pharmaceuticals and other chemicals could be tested for toxicity and effectiveness (Lysaught 1999). Some researchers believe that genetic alterations to embryonic stem cells could be used with the purpose of growing tissues with specific characteristics to compensate for defective tissues, and other envision genetic engineering of whole embryos (Lysaught 1999). Other possibilities include "the treatment of spinal cord injury, stroke, burns, arthritis, muscular dystrophy, kidney disease, liver disease, and macular degeneration" (Lysaught 1999).
Embryonic stem cells form at a very early stage in human development and remain in an undifferentiated state for a brief period (Wright 1999). They are first recognizable about five to seven days after fertilization, when a human embryo forms a blastocyst, a hollow, fluid-filled sphere, consisting of merely 140 cells, gives little indication that it could develop into a complete human being (Wright 1999). At this stage, there are two types of cells in the blastocyst:
Trophoblast cells, which form the "shell" of the sphere, will become the supporting tissues of the fetus such as the placenta.
Inner-cell-mass cells, which are located at one end within the blastocyst, are the undifferentiated cells that will divide and develop into the individual (Wright 1999).
When the inner cell mass begins to differentiate it forms the three fundamental germ layers of the embryo, the ectoderm, the mesoderm and the endoderm (Wright 1999). Each of these layers has a "specific destiny as a particular set of tissues in the mature individual, and all organs are ultimately derived from them," the ectoderm will form the skin, the eyes and the nervous system, the mesoderm will form bone, blood and muscle tissue, and the endoderm will develop into the lungs, liver, and lining of the gut (Wright 1999). These cells are considered to be totipotent because they rise to a complete individual, and when the inner cell mass cells are cultured in a dish, they are called embryonic stem cells (Wright 1999).
Up until the formation of the primitive streak, which will develop into the spinal cord, and cell differentiation, which occurs about fourteen days after fertilization, the developing embryo can cleave naturally or artificially, resulting in the production of identical siblings, therefore, embryonic cells that are still part of the inner cell mass are described as totipotent because they can give rise to new organisms (McCartney 2002). Another possibility during this stage is that two developing embryonic cell masses with different genotypes will fuse to form what is called a chimera, "an organism whose cells derive from two or more distinct zygote lineages" (McCartney 2002). After the cells have begun to differentiate and the primitive streak has formed, twinning and chimera formation are no longer possible (McCartney 2002).
The 2003 Hastings Case Report discussed several issues concerning stem cell research. One concern pointed out was that for biological reasons alone, stem cell-based therapies might not be available for every patient who could benefit, and depending on how the issue is addressed, might ultimately benefit primarily white Americans (Gearhart 2003). According to the report, the increase interest in establishing banks of stem cell lines to facilitate research and in anticipation of the eventual use of transplants, raises important questions of justice concerning who would stand to benefit from these banks and their research and therapeutic applications (Gearhart 2003). There is a question about who, financially, will have access to stem cell-based therapies and also since some nations have legislated against allowing the use of embryonic stem cells, there may be a question of who legally will have access to therapies derived from banked stem cell lines, "particularly those of embryonic derivation. The biological properties of stem cells themselves may make them less accessible to some potential recipients than to others, a situation we term the problem of biological access" (Gearhart 2003). The report cautions that unless the problem of biological access is carefully addressed, an American stem… READ MORE
Quoted Instructions for "Embryonic Stem Cell Research in November 1998" Assignment:
Review of historical aspects of Embryonic stem cell research , a discussion of recent and current research, and perspectives on where the area is going in the future.
6 reputable sources not more than 25 years old.
Books, scientific journals, discover, scientific american or science are all good sources.
Paper must be written in third (objective person) and past tense.
How to Reference "Embryonic Stem Cell Research in November 1998" Term Paper in a Bibliography
“Embryonic Stem Cell Research in November 1998.” A1-TermPaper.com, 2004, https://www.a1-termpaper.com/topics/essay/embryonic-stem-cell-research/9486069. Accessed 5 Jul 2024.
Related Term Papers:
Stem Cell Research Genetic Engineering, Genetic Modification Term Paper
Stem Cell Research
Genetic engineering, genetic modification, and gene splicing are terms used for the process of manipulating genes in an organism, generally outside the organism's normal reproductive process (Genetic… read more
Term Paper 5 pages (1336 words) Sources: 1+ Topic: Genetics / DNA / Genes / Heredity
Stem Cell Research Embryonic Stem Term Paper
Stem Cell Research
Embryonic stem-cell research is not practically 'embryonic' and most of the ethical refutations in respect of embryonic stem cell research could be settled by more research. Restricting… read more
Term Paper 8 pages (3558 words) Sources: 8 Topic: Biology / Life
Funding Stem Cell Research Embryonic Term Paper
Funding Stem Cell Research
Embryonic stem cell research is a very promising field of research when it comes to possibly finding a cure for more than 70 diseases once deemed… read more
Term Paper 7 pages (1888 words) Sources: 1+ Topic: Healthcare / Health / Obamacare
Stem Cell Policies Essay
Stem Cell Policies
Scientific Breakthrough
The issue of stem cell research burst on the scientific scene in November of 1998 when researchers first reported the isolation of human embryonic stem… read more
Essay 3 pages (914 words) Sources: 2 Style: MLA Topic: Disease / Virus / Disorder / Injury
Stem Cell Research Term Paper
Stem Cell Research has been the topic of passionate debate within the public and political arena. Due to its potential for treatment of various diseases and injuries, stem cell research… read more
Term Paper 8 pages (2420 words) Sources: 5 Style: MLA Topic: Abortion / Pro-Life / Pro-Choice
Fri, Jul 5, 2024
If you don't see the paper you need, we will write it for you!
We can write a new, 100% unique paper!