4.6 Article

Roles of Hydroxyapatite Allocation and Microgroove Dimension in Promoting Preosteoblastic Cell Functions on Photocured Polymer Nanocomposites through Nuclear Distribution and Alignment

期刊

LANGMUIR
卷 31, 期 9, 页码 2851-2860

出版社

AMER CHEMICAL SOC
DOI: 10.1021/la504994e

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资金

  1. National Science Foundation [DMR-11-06142]
  2. UT Office of Research
  3. International Science & Technology Cooperation Program of China [2010DFB70470]
  4. Innovation Team of Changjiang River Scientific Research Institute

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This study clarifies how hydroxyapatite (HA) allocation and microgroove dimension affect mouse preosteoblastic MC3T3-E1 cell functions on microgrooved substrates of polymer nanocomposites. Using replica molding from micromachined silicon wafer templates, we fabricated photocured poly(epsilon-caprolactone) triacrylate (PCLTA)/HA nanocomposite substrates with parallel microgrooves (two groove widths of 5 and 15 mu m and one groove depth of 5 mu m). Four types of microgrooved substrates were made: homogeneous ones of PCLTA and PCLTA/HA with uniform distribution and two heterogeneous laminated microgrooved substrates with HA only in the PCLTA matrix in the ridges or bottom. These substrates were used to regulate MC3T3-E1 cell attachment, proliferation, alignment, nuclear circularity and distribution, and mineralization. MC3T3-E1 cell attachment and proliferation were much higher on the microgrooved substrates of PCLTA/HA than on those of PCLTA, in particular, on the 5 mu m wide microgrooved substrate with PCLTA/HA ridges and PCLTA bottom. The shape and distribution of MC3T3-E1 cytoskeleton and nuclei were altered by the substrate topography and HA allocation. For 5 mu m wide heterogeneous microgrooved substrates with HA only in the ridges, MC3T3-E1 cells exhibited better spreading perpendicular to the microgrooves but tended to extend along the microgrooves containing HA in the bottom. The widest cells and the roundest/largest cell nuclei were observed on the heterogeneous substrate with PCLTA/HA ridges, while the narrowest cells with the best elongation were found on the homogeneous PCLTA/HA substrate. The trend in MC3T3-E1 cell mineralization on the substrates was consistent with that in cell/nuclear elongation. Osteocalcin mRNA expression was significantly higher on the PCLTA/HA substrates than on the PCLTA ones and also on the microgrooved substrates of PCLTA/HA than on the flat ones, regardless of the groove width of 5 or 15 mu m.

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