Alastair J. Sloan

Prof. Alastair J. Sloan

orcid

Research Focus & Metrics

Academic Career Length

29Years (1998-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 May 2006 in Biomaterials
Verified
Journal Article
Closed access
LGLee Graham
Lee Graham
Paul CooperPaul Cooper
Paul Cooper
NCNicola Cassidy
Nicola Cassidy
JNJacques E. Nor
Jacques E. Nor
ASAlastair J. Sloan
Alastair J. Sloan
ASAnthony J. Smith
Anthony J. Smith

1 August 2007 in Journal of Dentistry
Verified
Journal Article
Closed access
PTPhillip L. Tomson
Phillip L. Tomson
LGLiam M. Grover
Liam M. Grover
PLPhilip J. Lumley
Philip J. Lumley
ASAlastair J. Sloan
Alastair J. Sloan
ASAnthony J. Smith
Anthony J. Smith
Paul CooperPaul Cooper
Paul Cooper

1 April 2002 in Oral Surgery Oral Medicine Oral Pathology Oral Radiology and Endodontology
Verified
Journal Article
Closed access
PMPeter Murray
Peter Murray
HSHarold R. Stanley
Harold R. Stanley
JMJohn B. Matthews
John B. Matthews
ASAlastair J. Sloan
Alastair J. Sloan
ASAnthony J. Smith
Anthony J. Smith

1 February 1999 in Archives of Oral Biology
Verified
Journal Article
Closed access
ASAlastair J. Sloan
Alastair J. Sloan
ASA J Smith
A J Smith

14 August 2008 in Cells Tissues Organs
Verified
Journal Article
Closed access
RWRachel J. Waddington
Rachel J. Waddington
SYSarah J. Youde
Sarah J. Youde
CLChi P. Lee
Chi P. Lee
ASAlastair J. Sloan
Alastair J. Sloan
The present study compared the cellular characteristics of progenitor stem cell populations present in adult dental pulp, isolated by different methods utilizing 2 different features of stem cell biology. One population expressing high levels of β1 integrin was isolated by preferential selection of adherent cells to fibronectin over 20 min. In an alternative approach, cells expressing the embryonic neural crest cell marker, low-affinity nerve growth factor receptor (LANGFR), were selected by magnetic-activated cell sorting. For each method, clonal cell lines were established and expanded in culture. One clone derived via the respective methods was examined for embryonic/progenitor cell markers by immunocytochemistry and RT-PCR. Both clonal populations demonstrated the expression of stro-1 and stained positive for vimentin, demonstrating mesenchymal lineage. Of note, cells selected for LANGFR cells demonstrated the additional expression of CD105 and Notch 2. For both clonal populations, expanded cultures demonstrated the ability to differentiate into osteoblasts, adipocytes and chondrocytes. These results would suggest the potential isolation of 2 progenitor cell populations exhibiting different cellular characteristics in terms of their embryonic nature. The potential for both cell populations to derive from a common origin is discussed.

1 January 2002 in Connective Tissue Research
Verified
Journal Article
Closed access
KDK. Dobie
K. Dobie
GSG. Smith
G. Smith
ASAlastair J. Sloan
Alastair J. Sloan
ASA. J. Smith
A. J. Smith
The objective of this study was to investigate the use of alginate hydrogels to present either exogenous or endogenous transforming growth factor (TGF)-beta 1 to the dentin-pulp complex to signal reparative processes. Hydrogels were prepared, applied to cultured human tooth slices and the effects on tertiary dentinogenesis examined histologically. Both TGF-beta 1-containing and acid-treated alginate hydrogels, but not untreated hydrogels, upregulated dentin matrix secretion and induced odontoblast-like cell differentiation with subsequent secretion of regular tubular dentin matrix on cut pulpal surfaces. It is concluded that TGF-beta 1 can signal both induction of odontoblast-like cell differentiation and upregulation of their matrix secretion in the human dentin-pulp complex. Alginate hydrogels provide an appropriate matrix in which dental regeneration can take place and may also be useful for delivery of growth factors, including TGF-beta s, to enhance the natural regenerative capacity of the dental pulp.