Bruce Bunnell

Prof. Bruce Bunnell

Microbiology, Immunology and Genetics, University of North Texas Health Science Center, Fort Worth, Texas, USA
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Research Focus & Metrics

Academic Career Length

41Years (1986-Present)

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

Representative Publications

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11 May 2007 in Circulation Research
Verified
Journal Article
Closed access
PDF file
JGJeffrey M. Gimble
Jeffrey M. Gimble
AKAdam J. Katz
Adam J. Katz
Bruce BunnellBruce Bunnell
Bruce Bunnell
The emerging field of regenerative medicine will require a reliable source of stem cells in addition to biomaterial scaffolds and cytokine growth factors. Adipose tissue represents an abundant and accessible source of adult stem cells with the ability to differentiate along multiple lineage pathways. The isolation, characterization, and preclinical and clinical application of adipose-derived stem cells (ASCs) are reviewed in this article.

1 June 2013 in Cytotherapy
Verified
Journal Article
Open access
PBPhilippe Bourin
Philippe Bourin
Bruce BunnellBruce Bunnell
Bruce Bunnell
LCLouis Casteilla
Louis Casteilla
MDMassimo Dominici
Massimo Dominici
AKAdam J. Katz
Adam J. Katz
JGJeffrey M. Gimble
Jeffrey M. Gimble
Adipose tissue is a rich and very convenient source of cells for regenerative medicine therapeutic approaches. However, a characterization of the population of adipose-derived stromal and stem cells (ASCs) with the greatest therapeutic potential remains unclear. Under the authority of International Federation of Adipose Therapeutics and International Society for Cellular Therapy, this paper sets out to establish minimal definitions of stromal cells both as uncultured stromal vascular fraction (SVF) and as an adherent stromal/stem cells population. Phenotypic and functional criteria for the identification of adipose-derived cells were drawn from the literature. In the SVF, cells are identified phenotypically by the following markers: CD45-CD235a-CD31-CD34+. Added value may be provided by both a viability marker and the following surface antigens: CD13, CD73, CD90 and CD105. The fibroblastoid colony-forming unit assay permits the evaluation of progenitor frequency in the SVF population. In culture, ASCs retain markers in common with other mesenchymal stromal/stem cells (MSCs), including CD90, CD73, CD105, and CD44 and remain negative for CD45 and CD31. They can be distinguished from bone-marrow-derived MSCs by their positivity for CD36 and negativity for CD106. The CFU-F assay is recommended to calculate population doublings capacity of ASCs. The adipocytic, chondroblastic and osteoblastic differentiation assays serve to complete the cell identification and potency assessment in conjunction with a quantitative evaluation of the differentiation either biochemically or by reverse transcription polymerase chain reaction. The goal of this paper is to provide initial guidance for the scientific community working with adipose-derived cells and to facilitate development of international standards based on reproducible parameters.

1 June 2008 in Methods
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Journal Article
Closed access
Bruce BunnellBruce Bunnell
Bruce Bunnell
MFM Flaat
M Flaat
CGC Gagliardi
C Gagliardi
BPB Patel
B Patel
CRC Ripoll
C Ripoll

22 June 2006 in Journal of Cellular Biochemistry
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Journal Article
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RIReza Izadpanah
Reza Izadpanah
CTCynthia Trygg
Cynthia Trygg
BPBindiya Patel
Bindiya Patel
CKChristopher Kriedt
Christopher Kriedt
JDJason Dufour
Jason Dufour
Bruce BunnellBruce Bunnell
Bruce Bunnell

1 July 2007 in Biochemical and Biophysical Research Communications
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Journal Article
Closed access
WGWarren L. Grayson
Warren L. Grayson
FZFeng Zhao
Feng Zhao
Bruce BunnellBruce Bunnell
Bruce Bunnell
TMTeng Ma
Teng Ma

6 January 2015 in Nature Reviews Endocrinology
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Journal Article
Closed access
PDF file
WGWarren L. Grayson
Warren L. Grayson
Bruce BunnellBruce Bunnell
Bruce Bunnell
EMElizabeth Martin
Elizabeth Martin
TFTrivia Frazier
Trivia Frazier
BHBen P. Hung
Ben P. Hung
JGJeffrey M. Gimble
Jeffrey M. Gimble