Different Types Of Cell Research

Bone marrow transplants save a lot lives every year, a suitable donor is regrettably not always available. Since organs are routinely harvested from cadaveric organ donors, Scientists decided to assess such a possibility for bone marrow. They analyzed the functional properties and the phenotypic markers of hematopoietic stem and progenitor cells (HSPC) from cadaveric bone marrow. Fresh bone marrow was capable of growing and developing in cell suspension for 2

Hematopoietic stem cells are unspecialized cells that can develop into all types of blood cells, such as white blood cells, red blood cells, and platelets. These cells can be found in the peripheral blood, unbelicalcord and the bone marrow. There are four different types of hematopoietic stem cell (HSC) transplants. They are autologous transplant, allogeneic transplant, myeloablative transplant, non-myeloablative transplant.

All blood cells and components have vital roles making it necessary that they are replenished continuously; this is achieved by haematopoiesis, where there is a differentiation of a population of pluripotent cells, known as haematopoietic stem cells. HSCs are unspecialised cells that can be differentiated into multiple lineages (figure 1) of mature blood cells (Park et al., 2015). Not only do these cells possess the potential for multipotency they also have the ability of self-renewal, making them a suitable curative to be used in transplantation. Haematopoietic stem cell transplantation (HSCT) is an evolving technique which involves the intravenous infusion of HSCs designed to restore effective haematopoiesis, bone marrow and immune system

Attempts were made to fertilize mammalian eggs outside of the human body and in the early 1900s, it was discovered that some cells had the ability to generate blood cells. In 1968, the first bone marrow transplant was performed to successfully to treat patient’s severe combined immunodeficiency. There have been many stem cell discoveries since the early 1900’s but the two majors were in 1998 when, Thompson, from the University of Wisconsin, isolated cells from the inner cell mass of early embryos and developed the first embryonic stem cell lines. Then, in 1999 and 2000, scientists discovered that manipulating adult mouse tissues could produce different cell types.

A procedure known as transplantation consists of the transfer of cells, tissue or organ from one part of the body to another or from one person to another (National Cancer Institute, no date). Haemopoietic stem cells (HSCs) are unspecialized cells that have the ability to self-renew and the ability to differentiate into the HSCs lineage (Figure 1) for instance as white blood cells (WBCs), red blood cells (RBCs) and platelets. Treatment for a range of haematological disorders usually requires transfusion and transplantation (Knight, 2013). To obtain HSCs for transplantation there are three main sources. They are the bone marrow (BM), peripheral blood stem cells (PBSCs) and umbilical cord blood (UCB) (Smith and Wagner, 2010). A haploidentical donor is another source where the HLA match is not complete and there is a match of one haplotype. HSCs can be transplanted by an autologous, allogeneic and syngeneic donor (Hatzimichael and Tuthill, 2010). HSCs transplantation is carried out to eliminate the condition by myeloablation (prevent immune system attacking/rejecting new graft), to prevent the body being attacked by the new immune system derived from the new HSCs by graft versus host disease (GvHD) and to avoid rejection of the graft by immunosuppression (Buckland, 2017).

Many scientists believe that embryonic stem cell (ESC) research is the key to curing diseases such as cancer and HIV. Stem cells are so important to biomedical research because they are primitive cells that are capable of replicating indefinitely producing a multitude of different types of cells. This means that one of these pre-determined cells has to potential of becoming any range of over two hundred tissues with epithelial cells to blood and

Scientists are interested in stem cells for their ability to become any type of cell in the body, a process called differentiation. Theoretically, this allows for limitless possibilities in disease

When these problems occur in a person's lifetime, stem-cell based therapies can be an opportunity to solve these tragedies in life. Treatments are found in the branch of regenerative medicine and have just recently been successfully tested-the first bone-marrow cell transplantation was performed in the year 1957-on live patients with cancer. These therapies are discussed in further detail in the"IIV Stem Cell Transplantation" chapter.

The first and most evident issue relating to HES cell research is that by obtaining the embryonic stem cells it destroys potential human life. “Scientist discovered how to derive embryonic stem cells in 1981” (What Are).

Stem cells have the ability to develop into many different cell types in the human body, and are used as an internal repair system. By dividing itself, the stem cell can create two more cells that have the potential to either stay as a stem cell or evolve into another specialized cell such as a red blood cell, a brain cell, or a muscle cell.

These marrow failure syndromes include aplastic anemia, myelodysplastic syndrome, and acute myeloid leukemia all of which can only be cured with HSCT (Latour et al., 2015). If HSCT is not performed, the only remaining treatments are supportive. The process of HSCT is as follows: one and a half liters of stem cells and fluid are collected from the donor patient, usually from the pelvis, by needle aspiration. The transplant patient has to be admitted to a hospital ten days before the procedure to receive saline fluids, a central line, intensive chemotherapy, and immunosuppression. The chemotherapy can be with or without radiation and is used to ensure death of all of the damaged stem cells. Immunosuppression, by medicines or plasmapheresis, is used to ensure that the body does not reject the donor stem cells. After these steps have been completed, the donor stem cells will pass through a filter to remove bone fragments and fat cells and will eventually travel into the receiving patient’s bone marrow. The patient will stay in a sterile environment and will continue to receive transfusions until engraftment occurs. The patient’s platelets and red blood cells will fully recover in two to six months (Silverman et al., 2007). A case study done in 2005 reported that there had only been 24 stem cell transplantations for SDS patients. Of the 24

Stem cells are a class of non-specialized cells that can differentiate into almost any specialized cell in our body. They have the remarkable potential to

Stem cells are cells that have the capabilities to develop into many different types of cells in the body. Serving as a type of repair system for the body, they can theoretically divide without limit to take over for other cells for

that can be found in both children and adults. The difference between the two cells are the

Stem cell research is argued to be unethical and unnecessary, however, refusing to choose not to discover treatments for those who suffer is unethical and immoral. Stem cells are used for more than just research; once a specific study is complete and found to work, they use it on humans to treat diseases. Stem cells are used for development of many treatments for all kinds of patients. Stem cells are very popular in regards to patients with leukemia (Genetic Science Learning Center). Leukemia is a cancer of white blood cells which are the cells that are supposed to protect our bodies from diseases and foreign objects. With leukemia patients, their body is unable to fight off this disease. Chemotherapy and radiation are very common treatments for patients with cancer, however, it can be a very painful process for the patient (Genetics Science Learning Center).