Tissue Formation and Vascularization in Anatomically Shaped Human Joint Condyle Ectopically in Vivo

CH Lee, NW Marion, S Hollister, JJ Mao - Tissue engineering Part A, 2009 - liebertpub.com
CH Lee, NW Marion, S Hollister, JJ Mao
Tissue engineering Part A, 2009liebertpub.com
Scale-up of bioengineered grafts toward clinical applications is a challenge in regenerative
medicine. Here, we report tissue formation and vascularization of anatomically shaped
human tibial condyles ectopically with a dimension of 20× 15× 15 mm3. A composite of poly-
ɛ-caprolactone and hydroxyapatite was fabricated using layer deposition of three-
dimensional interlaid strands with interconnecting microchannels (400 μm) and seeded with
human bone marrow stem cells (hMSCs) with or without osteogenic differentiation. An …
Scale-up of bioengineered grafts toward clinical applications is a challenge in regenerative medicine. Here, we report tissue formation and vascularization of anatomically shaped human tibial condyles ectopically with a dimension of 20 × 15 × 15 mm3. A composite of poly-ɛ-caprolactone and hydroxyapatite was fabricated using layer deposition of three-dimensional interlaid strands with interconnecting microchannels (400 μm) and seeded with human bone marrow stem cells (hMSCs) with or without osteogenic differentiation. An overlaying layer (1 mm deep) of poly(ethylene glycol)-based hydrogel encapsulating hMSCs or hMSC-derived chondrocytes was molded into anatomic shape and anchored into microchannels by gel infusion. After 6 weeks of subcutaneous implantation in athymic rats, hMSCs generated not only significantly more blood vessels, but also significantly larger-diameter vessels than hMSC-derived osteoblasts, although hMSC-derived osteoblasts yielded mineralized tissue in microchannels. Chondrocytes in safranin-O-positive glycosaminoglycan matrix were present in the cartilage layer seeded with hMSC-derived chondrogenic cells, although significantly more cells were present in the cartilage layer seeded with hMSCs than hMSC-derived chondrocytes. Together, MSCs elaborate substantially more angiogenesis, whereas their progenies yield corresponding differentiated tissue phenotypes. Scale up is probable by incorporating a combination of stem cells and their progenies in repeating modules of internal microchannels.
Mary Ann Liebert