PMID- 9758040 OWN - NLM STAT- MEDLINE DCOM- 19981208 LR - 20220310 IS - 0142-9612 (Print) IS - 0142-9612 (Linking) VI - 19 IP - 15 DP - 1998 Aug TI - Three-dimensional culture of rat calvarial osteoblasts in porous biodegradable polymers. PG - 1405-12 AB - Neonatal rat calvarial osteoblasts were cultured in 90% porous, 75:25 poly(DL-lactic-co-glycolic acid) (PLGA) foam scaffolds for up to 56 days to examine the effects of the cell seeding density, scaffold pore size, and foam thickness on the proliferation and function of the cells in this three-dimensional environment. Osteoblasts were seeded at either 11.1 x 10(5) or 22.1 x 10(5) cells per cm2 onto PLGA scaffolds having pore sizes in the range of 150-300 or 500-710 microm with a thickness of either 1.9 or 3.2 mm. After 1 day in culture, 75.6 and 68.6% of the seeded cells attached and proliferated on the 1.9 mm thick scaffolds of 150-300 microm pore size for the low and high seeding densities, respectively. The number of osteoblasts continued to increase throughout the study and eventually leveled off near 56 days, as indicated by a quantitative DNA assay. Osteoblast/foam constructs with a low cell seeding density achieved comparable DNA content and alkaline phosphatase (ALPase) activity after 14 days, and mineralization results after 56 days to those with a high cell seeding density. A maximum penetration depth of osseous tissue of 220+/-40 microm was reached after 56 days in the osteoblast/foam constructs of 150-300 microm pore size initially seeded with a high cell density. For constructs of 500-710 microm pore size, the penetration depth was 190+/-40 microm under the same conditions. Scaffold pore size and thickness did not significantly affect the proliferation or function of osteoblasts as demonstrated by DNA content, ALPase activity, and mineralized tissue formation. These data show that comparable bone-like tissues can be engineered in vitro over a 56 day period using different rat calvarial osteoblast seeding densities onto biodegradable polymer scaffolds with pore sizes in the range of 150-710 microm. When compared with the results of a previous study where similar polymer scaffolds were seeded and cultured with marrow stromal cells, this study demonstrates that PLGA foams are suitable substrates for osteoblast growth and differentiated function independent of cell source. FAU - Ishaug-Riley, S L AU - Ishaug-Riley SL AD - Institute of Biosciences and Bioengineering and Department of Chemical Engineering, Rice University, Houston, TX 77005-1892, USA. FAU - Crane-Kruger, G M AU - Crane-Kruger GM FAU - Yaszemski, M J AU - Yaszemski MJ FAU - Mikos, A G AU - Mikos AG LA - eng GR - R29-AR42639/AR/NIAMS NIH HHS/United States PT - Journal Article PT - Research Support, U.S. Gov't, Non-P.H.S. PT - Research Support, U.S. Gov't, P.H.S. PL - Netherlands TA - Biomaterials JT - Biomaterials JID - 8100316 RN - 0 (Biocompatible Materials) RN - 0 (Polymers) RN - 1SIA8062RS (Polylactic Acid-Polyglycolic Acid Copolymer) RN - 26009-03-0 (Polyglycolic Acid) RN - 33X04XA5AT (Lactic Acid) RN - EC 3.1.3.1 (Alkaline Phosphatase) SB - IM MH - Alkaline Phosphatase/metabolism MH - Animals MH - *Biocompatible Materials MH - Bone Development/physiology MH - Bone Matrix/*cytology MH - Cell Adhesion/physiology MH - Cell Count MH - Cell Division/physiology MH - Cells, Cultured MH - *Lactic Acid MH - Osteoblasts/*cytology/enzymology MH - *Polyglycolic Acid MH - Polylactic Acid-Polyglycolic Acid Copolymer MH - *Polymers MH - Rats MH - Rats, Sprague-Dawley OTO - NASA OT - NASA Discipline Cell Biology OT - Non-NASA Center FIR - Mikos, A G IR - Mikos AG IRAD- Rice U, Houston, TX EDAT- 1998/10/03 00:00 MHDA- 1998/10/03 00:01 CRDT- 1998/10/03 00:00 PHST- 1998/10/03 00:00 [pubmed] PHST- 1998/10/03 00:01 [medline] PHST- 1998/10/03 00:00 [entrez] AID - S0142-9612(98)00021-0 [pii] AID - 10.1016/s0142-9612(98)00021-0 [doi] PST - ppublish SO - Biomaterials. 1998 Aug;19(15):1405-12. doi: 10.1016/s0142-9612(98)00021-0.