Paul Thomas Sharpe | |
---|---|
Born | |
Nationality | British |
Known for | Cellular differentiation |
Spouse | Joy Elizabeth Sharpe (nee Mitchell) |
Academic background | |
Alma mater | University of York University of Sheffield |
Thesis | Differentiation of the cellular slime mould Dictyostelium discoideum (1981) |
Doctoral advisor | Donald J. Watt |
Academic work | |
Discipline | Biology |
Institutions | King's College London |
Website | www |
Paul Thomas Sharpe (born 12 December 1955) is a British biologist who is the Dickinson Professor of Craniofacial Biology and Director,Centre for Craniofacial and Regenerative Biology,King's College London. [1]
Sharpe was educated at De La Salle College,Sheffield (now All Saints Catholic High School,Sheffield) (1967-1974). He holds a BA in Biology from the University of York (1977) and a PhD from the University of Sheffield (1981).[ citation needed ]
Following his doctoral work at the University of Sheffield,Sharpe continued as a postdoctoral researcher there and also at the University of Wisconsin and the University of Cambridge prior to his first academic appointment at the University of Manchester (1997). Sharpe's research focuses on cell differentiation and began with his doctoral work on differentiation of the cellular slime mould Dictyostelium discoideum but he extended this work to mammalian tissues,principally bone. [2] [3] In this early work he applied the technique of thin layer countercurrent distribution. [4] [5] Subsequently,through the study of mouse embryo differentiation and the role of homeobox sequences in DNA,his work has mainly been applied to the field of craniofacial development. [6] [7] Most recently he has been leading research into the possibility of tooth regeneration and the development of new biological-based treatments for tooth repair. [8] [9] [10] [11] [12] Sharpe is author of Methods of Cell Separation. [13]
Sharpe is an Honorary Fellow of the Royal College of Surgeons in Edinburgh (2010) and a recipient of the Gregor Mendel Memorial Medal (2003). [14] He was awarded the Craniofacial Biology Research Award by the International Association for Dental Research (2004) and 2018 he received the William J Gies award for best publication is Biomaterials and Bioengineering (2018). [15]
Sharpe (stage name Paul Shaft) is a musician and was a pioneer of the Sheffield punk music and new wave music scene. Originally he played bass guitar in the Sheffield band 2.3 and then formed the avant-garde band De Tian. [16] [17] He later played double bass and sang in the experimental jazz influenced band,Bass Tone Trap. [18] Sharpe (Shaft) reformed 2.3 in 2018 and they have released two albums. [19] [20] Sharpe,a lifelong supporter of Sheffield United F.C. is married to Joy Elizabeth Sharpe (nee Mitchell) and they have two children. [21]
Sharpe has over 300 publications listed on Web of Science which have been cited more than 14,500 times;his h-index is 66. His three most-cited articles are:
A homeobox is a DNA sequence, around 180 base pairs long, that regulates large-scale anatomical features in the early stages of embryonic development. Mutations in a homeobox may change large-scale anatomical features of the full-grown organism.
Dictyostelium is a genus of single- and multi-celled eukaryotic, phagotrophic bacterivores. Though they are Protista and in no way fungal, they traditionally are known as "slime molds". They are present in most terrestrial ecosystems as a normal and often abundant component of the soil microflora, and play an important role in the maintenance of balanced bacterial populations in soils.
Hox genes, a subset of homeobox genes, are a group of related genes that specify regions of the body plan of an embryo along the head-tail axis of animals. Hox proteins encode and specify the characteristics of 'position', ensuring that the correct structures form in the correct places of the body. For example, Hox genes in insects specify which appendages form on a segment, and Hox genes in vertebrates specify the types and shape of vertebrae that will form. In segmented animals, Hox proteins thus confer segmental or positional identity, but do not form the actual segments themselves.
The zona limitans intrathalamica (ZLI) is a lineage-restriction compartment and primary developmental boundary in the vertebrate forebrain that serves as a signaling center and a restrictive border between the thalamus and the prethalamus.
Homeobox protein MSX-1, is a protein that in humans is encoded by the MSX1 gene. MSX1 transcripts are not only found in thyrotrope-derived TSH cells, but also in the TtT97 thyrotropic tumor, which is a well differentiated hyperplastic tissue that produces both TSHß- and a-subunits and is responsive to thyroid hormone. MSX1 is also expressed in highly differentiated pituitary cells which until recently was thought to be expressed exclusively during embryogenesis. There is a highly conserved structural organization of the members of the MSX family of genes and their abundant expression at sites of inductive cell–cell interactions in the embryo suggest that they have a pivotal role during early development.
Paired-like homeodomain transcription factor 2 also known as pituitary homeobox 2 is a protein that in humans is encoded by the PITX2 gene.
Homeobox protein MSX-2 is a protein that in humans is encoded by the MSX2 gene.
Homeobox protein Hox-B6 is a protein that in humans is encoded by the HOXB6 gene.
Homeobox D10, also known as HOXD10, is a protein which in humans is encoded by the HOXD10 gene.
Homeobox protein Hox-A7 is a protein that in humans is encoded by the HOXA7 gene.
Homeobox protein DLX-5 is a protein that in humans is encoded by the distal-less homeobox 5 gene, or DLX5 gene. DLX5 is a member of DLX gene family.
Homeobox protein DLX-3 is a protein that in humans is encoded by the DLX3 gene.
Paired related homeobox 1 is a protein that in humans is encoded by the PRRX1 gene.
Dictyostelium discoideum is a species of soil-dwelling amoeba belonging to the phylum Amoebozoa, infraphylum Mycetozoa. Commonly referred to as slime mold, D. discoideum is a eukaryote that transitions from a collection of unicellular amoebae into a multicellular slug and then into a fruiting body within its lifetime. Its unique asexual life cycle consists of four stages: vegetative, aggregation, migration, and culmination. The life cycle of D. discoideum is relatively short, which allows for timely viewing of all stages. The cells involved in the life cycle undergo movement, chemical signaling, and development, which are applicable to human cancer research. The simplicity of its life cycle makes D. discoideum a valuable model organism to study genetic, cellular, and biochemical processes in other organisms.
Homeobox protein GBX-2 is a protein that in humans is encoded by the GBX2 gene.
Dental pulp stem cells (DPSCs) are stem cells present in the dental pulp, which is the soft living tissue within teeth. DPSCs can be collected from dental pulp by means of a non-invasive practice. It can be performed with an adult after simple extraction or to the young after surgical extraction of wisdom teeth. They are pluripotent, as they can form embryoid body-like structures (EBs) in vitro and teratoma-like structures that contained tissues derived from all three embryonic germ layers when injected in nude mice. DPSCs can differentiate in vitro into tissues that have similar characteristics to mesoderm, endoderm and ectoderm layers. They can differentiate into many cell types, such as odontoblasts, neural progenitors, osteoblasts, chondrocytes, and adipocytes. DPSCs were found to be able to differentiate into adipocytes and neural-like cells. These cells can be obtained from postnatal teeth, wisdom teeth, and deciduous teeth, providing researchers with a non-invasive method of extracting stem cells. The different cell populations, however, differ in certain aspects of their growth rate in culture, marker gene expression and cell differentiation, although the extent to which these differences can be attributed to tissue of origin, function or culture conditions remains unclear. As a result, DPSCs have been thought of as an extremely promising source of cells used in endogenous tissue engineering.
Homeotic genes are genes which regulate the development of anatomical structures in various organisms such as echinoderms, insects, mammals, and plants. Homeotic genes often encode transcription factor proteins, and these proteins affect development by regulating downstream gene networks involved in body patterning.
Athanasia Papalopulu is a Wellcome Trust senior research fellow and Professor of Developmental Neuroscience in the School of Biological Sciences, University of Manchester.
Hox genes play a massive role in some amphibians and reptiles in their ability to regenerate lost limbs, especially HoxA and HoxD genes.
Craniofacial regeneration refers to the biological process by which the skull and face regrow to heal an injury. This page covers birth defects and injuries related to the craniofacial region, the mechanisms behind the regeneration, the medical application of these processes, and the scientific research conducted on this specific regeneration. This regeneration is not to be confused with tooth regeneration. Craniofacial regrowth is broadly related to the mechanisms of general bone healing.