This report reviews three categories of precursor cells present within adults. The first category of precursor cell, the epiblast-like stem cell, has the potential of forming cells from all three embryonic germ layer lineages, e.g., ectoderm, mesoderm, and endoderm. The second category of precursor cell, the germ layer lineage stem cell, consists of three separate cells. Each of the three cells is committed to form cells limited to a specific embryonic germ layer lineage. Thus the second category consists of germ layer lineage ectodermal stem cells, germ layer lineage mesodermal stem cells, and germ layer lineage endodermal stem cells. The third category of precursor cells, progenitor cells, contains a multitude of cells. These cells are committed to form specific cell and tissue types and are the immediate precursors to the differentiated cells and tissues of the adult. The three categories of precursor cells can be readily isolated from adult tissues. They can be distinguished from each other based on their size, growth in cell culture, expressed genes, cell surface markers, and potential for differentiation. This report also discusses new findings. These findings include the karyotypic analysis of germ layer lineage stem cells; the appearance of dopaminergic neurons after implantation of naive adult pluripotent stem cells into a 6-hydroxydopamine-lesioned Parkinson's model; and the use of adult stem cells as transport mechanisms for exogenous genetic material. We conclude by discussing the potential roles of adult-derived precursor cells as building blocks for tissue repair and as delivery vehicles for molecular medicine.
We describe a new species of chorus frog of the North American treefrog genus Pseudacris from the south-central United States. This new species is morphologically similar to the parapatric species P. feriarum and has thus previously been considered synonymous with this species. The new species is geographically distinct from P. feriarum and from its sister species, P. nigrita. We diagnose the new species based on advertisement call, morphological, and genetic characters.
A series of 5-[1-[4-[(4,5-disubstituted-1H-imidazol-1-yl)methyl]- substituted]-1H-pyrrol-2-yl]-1H-tetrazoles and 5-[1-[4-[(3,5-dibutyl-1H-1,2,4-triazol-1-yl)methyl]-substituted]- 1H-pyrrol-2-yl]-1H-tetrazoles were investigated as novel AT1-selective angiotensin II receptor antagonists. Computer-assisted modeling techniques were used to evaluate structural parameters in comparison to the related biphenyl system. New synthetic procedures have been developed to prepare the novel compounds. The best antagonists in this series had IC50 values (rat uterine membrane receptor binding) in the 10(-8) M range and corresponding pA2 in isolated organ assay (rabbit aorta rings). Structure-activity relationships indicate some similarities with the finding in the biphenyl system. Substitution on the pyrrole ring modulates activity. Compound 5 antagonized angiotensin-induced blood pressure increase when administered to conscious rat at 30 mg/kg per os.
This study was designed to determine if trauma causes the release of adult-derived blastomere-like stem cells (BLSCs) from skeletal muscle into the circulating blood of adult pigs. Experimental procedures followed the guidelines of Fort Valley State University's Institutional Animal Care and Utilization Committee. Pigs were traumatized by splenectomy followed by pancreatectomy. Blood samples and skeletal muscle biopsies were taken before and after trauma. Adult-derived BLSCs were isolated from skeletal muscle and blood samples following established procedures. Nontraumatized skeletal muscle contained approximately 277 million BLSCs per gram of muscle. After trauma, skeletal muscle contained approximately 2 million BLSCs per gram of muscle. Blood taken before trauma contained approximately 22 million BLSCs per milliliter, whereas approximately 512 million BLSCs per milliliter were present within the blood after trauma. Blood values were statistically significant with a P < 0.05. This report is the first demonstration that trauma causes the release of adult-derived BLSCs from skeletal muscle into blood. Further studies are required to elucidate the roles that adult-derived BLSCs play in the response to injury and in the healing process. Surgeons must take a role in this evolving field.
Millions of people throughout the tropics consume wild meat. Overhunting reduces food security for people and large predators, yet little is known of the impact of hunting in systems where people and predators target the same prey species. We collate published data on predator diet in Belize with interview data about the consumption of wild and domestic meat by Belizeans, to compare the wild-meat diets of humans, jaguars Panthera onca and pumas Puma concolor and assess the sustainability of the combined offtake by humans and jaguars. Six wild mammal species (nine-banded armadillo Dasypus novemcinctus, paca Cuniculus paca, collared peccary Pecari tajacu, white-lipped peccary Tayassu pecari, red brocket deer Mazama americana and white-tailed deer Odocoileus virginianus) comprised 7% of the animal-protein meals eaten by Belizeans. Overall, 80% of these meals were eaten by 20% of interviewees, suggesting a necessary role of wild meat for the minority. The same species were found in 69 and 86% of jaguar and puma scats, respectively. We estimate a national annual harvest of c. 4,000 tonnes of these six wild mammals by humans and jaguars, of which 78% is hunted by people. Sustainability is difficult to evaluate because prey population data are lacking in Belize. However, simple models suggest that a sustainable harvest at this rate would require higher prey population densities than averages recorded in hunted Neotropical forests. We emphasize the need for robust regional estimates of game species densities, to improve assessments of sustainability and inform hunting regulations. We recommend that the requirements of predators as well as those of people be considered when assessing wild meat harvests.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.