Literature DB >> 20871482

Direct comparison of progenitor cells derived from adipose, muscle, and bone marrow from wild-type or craniosynostotic rabbits.

Gregory M Cooper1, Emily L Durham, James J Cray, Michael R Bykowski, Gary E DeCesare, Melissa A Smalley, Mark P Mooney, Phil G Campbell, Joseph E Losee.   

Abstract

BACKGROUND: Reports have identified cells capable of osteogenic differentiation in bone marrow, muscle, and adipose tissues, but there are few direct comparisons of these different cell types. Also, few have investigated the potential connection between a tissue-specific abnormality and cells derived from seemingly unrelated tissues. In this article, the authors compare cells isolated from wild-type rabbits or rabbits with nonsyndromic craniosynostosis, defined as the premature fusion of one or more of the cranial sutures.
METHODS: Cells were derived from bone marrow, adipose, and muscle of 10-day-old wild-type rabbits (n = 17) or from age-matched rabbits with familial nonsyndromic craniosynostosis (n = 18). Cells were stimulated with bone morphogenetic protein-4 (BMP4), and alkaline phosphatase expression and cell proliferation were assessed.
RESULTS: In wild-type rabbits, cells derived from muscle had more alkaline phosphatase activity than cells derived from either adipose or bone marrow. The cells derived from craniosynostotic rabbit bone marrow and muscle were significantly more osteogenic than those derived from wild-type rabbits. Adipose-derived cells demonstrated no significant differences. Although muscle-derived cells were most osteogenic in wild-type rabbits, bone marrow-derived cells were most osteogenic in craniosynostotic rabbits.
CONCLUSIONS: These results suggest that cells from different tissues have different potentials for differentiation. Furthermore, cells derived from rabbits with craniosynostosis were different from cells from wild-type rabbits. Interestingly, cells derived from the craniosynostotic rabbits were not uniformly more responsive compared with wild-type cells, suggesting that specific tissue-derived cells may react differently in individuals with craniosynostosis.

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Year:  2011        PMID: 20871482      PMCID: PMC3015002          DOI: 10.1097/PRS.0b013e3181fad311

Source DB:  PubMed          Journal:  Plast Reconstr Surg        ISSN: 0032-1052            Impact factor:   4.730


  54 in total

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4.  Coronal suture pathology and synostotic progression in rabbits with congenital craniosynostosis.

Authors:  M P Mooney; T D Smith; A M Burrows; H L Langdon; C E Stone; H W Losken; K Caruso; M I Siegel
Journal:  Cleft Palate Craniofac J       Date:  1996-09

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  9 in total

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2.  Regression modeling to inform cell incorporation into therapies for craniosynostosis.

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Journal:  J Craniofac Surg       Date:  2013-01       Impact factor: 1.046

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5.  Development of mRuby2-Transfected C3H10T1/2 Fibroblasts for Musculoskeletal Tissue Engineering.

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7.  Adipose Stem Cells Display Higher Regenerative Capacities and More Adaptable Electro-Kinetic Properties Compared to Bone Marrow-Derived Mesenchymal Stromal Cells.

Authors:  Ahmed El-Badawy; Marwa Amer; Reda Abdelbaset; Sameh N Sherif; Marwan Abo-Elela; Yehya H Ghallab; Hamdy Abdelhamid; Yehea Ismail; Nagwa El-Badri
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8.  Tissue source determines the differentiation potentials of mesenchymal stem cells: a comparative study of human mesenchymal stem cells from bone marrow and adipose tissue.

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9.  Efficient reprogramming of naïve-like induced pluripotent stem cells from porcine adipose-derived stem cells with a feeder-independent and serum-free system.

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  9 in total

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