Induced Pluripotent Stem Cells And The Maintenance Of Neural Crest Stem Cell

Others develop into muscle cells that can contract and also into nerve cells. Because they have the potential to become such a wide variety of specialized cells, embryonic stem cells are described as pluripotent. Plurip.0otency is one of two key features of embryonic stem cells. The second key feature of embryonic stem cells is their ability to divide or self renew for an indefinite period while retaining their undifferentiated, pluripotent state. As the cell mass grows, the population can be further expanded by growing in larger tissue culture flasks. An unlimited number of undifferentiated, pluripotent stem cells can be produced (Sumanas Inc. 2007).

Pluripotent stem cells are just like Totipotent cells, but they can only become cell derived from the three germ layers, which contain over 200 specialized cells. Multipotent stem cells can only become blood cells, such as red blood cells, white blood cells, or platelets. Unipotent stem cells can only transform into one type of tissue or specialized cell, but it can divide over and over again (Wikipedia). These embryonic stem cells can divide again and again through mitosis (a type of cell division in all body parts except reproductive parts). Medical specialists and leading scientists conclude, that these cells could help cure as many as seventy-three diseases, which up to now were thought incurable (NIH).

Pluripotent stem cells are the stem cells that can only differentiate into a limited range of differentiated cells. (2) They have the ability to give rise to all somatic cells from ectoderm, mesoderm and endoderm, as well as gametes. Naturally it can be found in embryos as Embryonic stem cells (ES cells). Induced pluripotent stem cells (iPS cells or iPSC) are the pluripotent stem cells that are generated directly from adult cells, first discovered by Shinya Yamanaka in 2006 by using a set of reprogramming factors (Oct4, Sox2, Klf4, and c-Myc or LIN28 and Nanog) (3) to reprogram mature cells back to a pluripotent state (4).

There are many different types of stem-cells which can be implanted in patients to regenerate or replace the damaged or abnormal cells caused by not only diseases like Parkinson's but also Alzheimer's and spinal cord injuries (2). A specific example in relation to Parkinson's is the harvesting of embryonic stem cells. These human embryonic stem cells can be transplanted into the brain to replace and create dopamine neurons. The controversy is in how one can obtain these stem cells. During fertilization, in humans, the embryo is hollow and contains cells that eventually develop into a fetus (1). Researchers have discovered, as recently as 1998, that the cells in the embryo contain all

Embryonic stem cells (hESC) are pluripotent. They are obtained from the inner mass of a 5-6 day old human blastocyst that consists of approximately 100 cells (Bongso & Lee, 2005, p. 3).

Embryonic stem cells are found in human blastocysts (Marcovitz 17). A blastocyst is a very young embryo (just a few days old) that contains around 200 undifferentiated stem cells (Marcovitz 17). German Zoologist Valentin Hacker coined the term “stem cell” after he discovered them in a blastocyst of a crustacean (Marcovitz 18). Embryonic stem cells were collected for the first time in 1988 by Dr. James Thomson of University of Wisconsin and by Dr. John Gearheart of Johns Hopkins (Panno 76). These stem cells are unspecialized; they do not perform a specific function like cells such as muscle and nerve do (“Stem Cells”). They are also pluripotent, meaning they have the ability to divide and become specialized cells (“Stem Cells”). This is why stem cells hold so

To give a short overview of the steps that will be taken to complete the study. Obtaining stem cells, whether adult, embryonic or induced, shall be done using healthy mouse models and after ethical approval has been gained. The process to derive them will be detailed below, however they are also purchasable commercially with the benefit of being well studied and accompanied by a detailed analysis of properties, however with a

. Embryonic stem cells have been identified by scientist as a type of stem cell that can advance regenerative medicine. The potential of regenerative medicine ranges from allowing pancreatic cells to produce insulin for diabetics to reconnecting the nerves in severed spinal cords. However, the greatest potential embryonic stem cells presents are its ability to change into any of the more than 200 different cell types in the body. This ability to change into any cell type can produce cures for Alzheimer’s disease, Parkinson’s disease, or any of the other conditions that stem cell therapy might help therefore improving the lives of those who live with these

Stem cell research is the future of medical and biological research and remedies, and it is fascinating to watch the progression of this new and important science as it unfolds. These cells were discovered in mouse embryos in the 1980s, and are remarkable because of their potential to grow into a variety of different kinds of cells within a body. Common in fetuses, and more rare in adult animals of all kinds, stem cells can be manipulated in useful ways to repair many tissues, dividing limitlessly for therapeutic purposes. When a stem cell divides, each new cell has the potential either to remain a stem cell or to differentiate into more specialized tissue, such as nerve, pancreas, bone marrow, or unique blood components. Initially

The creation of induced pluripotent stem cells by direct reprogramming has allowed for the circumvention of using embryonic stem cells while still leaving the cells with the ability to maintain pluripotency. Instead of ES cells which were originally derived from the epiblast of mouse embryos, IPS cells were generated from mouse embryonic fibroblasts. This eliminated both any ethical concerns for whether those cells were a living being or not and the need to destroy embryos at the blastocyst stage. An advantage of IPS cells is that they are derived from human somatic cells which makes them easy to acquire due to the possibility of using skin or blood cells. They can also be grown and differentiated individually for each person that the sample of somatic cells is taken from which eliminates the possibility of having any immune reaction and rejection to the differentiated cells during transplantation. These characteristics of IPS cells are important because they are what enables us to safely and accurately transform these affected cells from patients cells into neurons and confidently study them.

Researchers successfully attained embryonic stem cells from the embryos of mice in 1981, which led to the discovery of this process in human beings in 1998 (National Institutes of Health, 2001). Embryonic stem cells are derived from an in vitro embryo between five days and seven weeks. Regenerative medicine can benefit greatly from the characteristics of embryonic stem cells. This process enables damaged organs and tissues to heal themselves with the help of implanted stem cells matching the organ (Hunziker, 2010, p. 1). There are two traits

When the topic of stem cell research, and/ or treatment, people generally automatically jump to the conclusion of embryonic stem cells, when in retrospect according to Eurostemcell.org, an organization based website that is dedicated to supplying the public with the latest news and information on stem cells. According to the article there a few different types of stem cells. The first type of stem cell is, embryonic. Embryonic stem cells are grown in a laboratory from embryos cells at an early stage. The second type of stem cell is tissue stem cells. Tissue stem cells are found in all different parts of the body. Lastly the third type of stem cell is, Induced pluripotent stem cell (iPS), or 'reprogrammed' stem cells. IPSC are similar to embryonic stem cells but they are from adult specialized cells.

The ability to manipulate the stem cell corresponding to a specific organ/tissue remains important. A type of stem cell that can be manipulated is the embryonic stem cell. These stem cells descend from embryos aging from three to five days (Watt) (Driskell). During earlier stages, scientists describe embryonic stem cells as “blastocysts” which contain over one-hundred and fifty cells (Watt) (Driskell). They duplicate into more cells or transform to any cell located in the body (Watt) (Driskell). This “duplication” allows embryonic stem cells to regenerate and repair diseased tissues. Embryonic stem cells gain importance in cancer treatments—if doctors diagnose patients with leukemia, then during chemotherapy, the doctor can infuse embryonic stem cells into the body. Since the cells are young, they can repair the targeted cell, aiding cancer treatments and the patient. In addition, this technique is used with another type of embryonic stem cell called “pluripotent stem cells”. Pluripotent stem cells originate as inner mast cells (cells

In 1981, scientists began to derive embryonic stem cells from mouse embryos. A decade later a more in depth study was discovered to be able to take human embryonic stem cells and grow them in laboratories. At first, the discovery was used only for in vitro fertilization procedures but until recently, in 2006, scientists made a breakthrough of embryonic stem cells used to be reprogrammed genetically with specialized adult cells. Embryonic stem cells, also known as pluripotent cells, can generate to become about two hundred types of cells in a human body and can specialize to do what they were programmed to do. This is due to the fact that embryonic stem cells can grow in large sums of numbers. Because of their ability to generate into specific

iPSCs are adult stem cells that have been genetically reprogrammed to behave like the pluripotent stem cells found in embryos, i.e. can differentiate into any cell type in the human body. This was first completed successfully in mice in 2006 by Shinya Yamanaka and his team (Takahashi et al., 2006), then in humans in 2007 both by Yamanaka (Takahashi et al., 2007), and by James Thomson and his team in America independently (Yu, et al., 2007). Yamanaka and Thomson’s methods were similar. In the report by Yu et