2006
DOI: 10.1016/j.biomaterials.2006.07.015
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Bone and cartilage tissue constructs grown using human bone marrow stromal cells, silk scaffolds and rotating bioreactors

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Cited by 173 publications
(148 citation statements)
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References 71 publications
(132 reference statements)
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“…In these cases, the goal is to produce a neo-formed tissue in vitro for later implantation in vivo. 70,71 Regardless of the method used to regenerate diseased or damaged musculoskeletal tissue, a common element in all of these cases is the use of inductive factors. Cells that are implanted either directly into the defect or first within a scaffold, as well as cells from the host that are recruited to the site of injury, all require stimulation by growth factors or morphogens to help in the formation of newly formed tissue.…”
Section: Discussionmentioning
confidence: 99%
“…In these cases, the goal is to produce a neo-formed tissue in vitro for later implantation in vivo. 70,71 Regardless of the method used to regenerate diseased or damaged musculoskeletal tissue, a common element in all of these cases is the use of inductive factors. Cells that are implanted either directly into the defect or first within a scaffold, as well as cells from the host that are recruited to the site of injury, all require stimulation by growth factors or morphogens to help in the formation of newly formed tissue.…”
Section: Discussionmentioning
confidence: 99%
“…We selected the cell source (hMSCs), scaffold type (porous silk) and bioreactor system (rotating vessels) based on our previous studies of tissue-engineered cartilage-and bone-like tissues. In these studies, hMSCs were shown to differentiate into chondrogenic and osteogenic lineages when cultured on silk scaffolds and subjected to chondrogenic or osteogenic regulatory factors (Meinel et al 2004a-c;Kim et al 2005a;Wang et al 2005;Hofmann et al 2006;Marolt et al 2006).…”
Section: Introductionmentioning
confidence: 99%
“…Yoshioka and colleagues [32] reported successful regeneration of cartilage in osteochondral-defective Japanese white rabbits using cartilaginous constructs obtained from culturing BMSCs. Yoshioka and colleagues culturing human BMSCs on a silk scaffold for 5 weeks produced 8 mm diameter by 2 mm thick cartilaginous constructs [33].…”
Section: Rotating Wall Vesselmentioning
confidence: 99%