Biomedical Engineering Reference
In-Depth Information
ECM. The implant temporarily supports initial
cell attachment and subsequent proliferation
and differentiation. Resident cells surrounding
the scaffold, or cells preseeded in the scaffold,
will proliferate and differentiate on the founda-
tion of a compatible scaffold. In some cases,
a scaffold and bonelike cells are not enough,
and supplementation with growth factors is
required.
In this chapter, we have focused on the metal
titanium fi ber mesh used as a scaffold material
for bone reconstruction either by loading it
with cells or by loading it with growth factors.
The results of the various studies clearly dem-
onstrated the excellent characteristics of tita-
nium fi ber mesh: biocompatibility, strength,
low stiffness, high porosity, and high coeffi cient
of friction. Further, cell-loaded meshes initi-
ated bone formation at orthotopic and ectopic
sites, and these cell-loaded meshes were shown
to be further optimized by dynamic seeding,
culturing, and addition of an ECM coating. The
growth-factor-loaded meshes showed increased
bone formation in comparison with unloaded
meshes when implanted either subcutaneously
or in a cranial defect. In summary, titanium
fi ber mesh is a useful scaffold material that
warrants further investigation as a clinical tool
for bone reconstructive surgery.
6. Bruder SP, Jaiswal N, Haynesworth SE (1997) Growth
kinetics, self-renewal, and the osteogenic potential of
purifi ed human mesenchymal stem cells during
extensive subcultivation and following cryopreserva-
tion. J Cell Biochem 64:278-294.
7. Chang YS, Oka M, Kobayashi M, Gu HO, Li ZL,
Nakamura T, Ikada Y (1996) Signifi cance of intersti-
tial bone ingrowth under load-bearing conditions: a
comparison between solid and porous implant mate-
rials. Biomaterials 17:1141-1148.
8. Cohen R (2002) A porous tantalum trabecular metal:
basic science. Am J Orthop 31:216-217.
9. Gao JM, Niklason L, Langer R (1998) Surface hydro-
lysis of poly(glycolic acid) meshes increases the
seeding density of vascular smooth muscle cells.
J Biomed Mater Res 42:417-424.
10. Goldstein AS, Juarez TM, Helmke CD, Gustin MC,
Mikos AG (2001) Effect of convection on osteoblastic
cell growth and function in biodegradable polymer
foam scaffolds. Biomaterials 22:1279-1288.
11. Hanada K, Dennis JE, Caplan I (1997) Stimulatory
effects of basic fi broblast growth factor and bone mor-
phogenetic protein-2 on osteogenic differentiation of
rat bone marrow derived mesenchymal stem cells.
J Bone Miner Res 12:1606 -1614.
12. Haynesworth SE, Goshima J, Goldberg VM, Caplan AI
(1992) Characterization of cells with osteogenic poten-
tial from human marrow. Bone 13:81-88.
13. Holy CE, Shoichet MS, Davies JE (2000) Engineering
three-dimensional bone tissue in vitro using biode-
gradable scaffolds: investigating initial cell-seeding
density and culture period. J Biomed Mater Res
51:376-382.
14. Ishaug SL, Crane GM, Miller MJ, Yasko AW,
Yaszemski MJ, Mikos AG (1997) Bone formation by
three-dimensional stromal osteoblast culture in bio-
degradable polymer scaffolds. J Biomed Mater Res
36:17-28.
15. Jaiswal N, Haynesworth SE, Caplan AI, Bruder SP
(1997) Osteogenic differentiation of purifi ed, culture-
expanded human mesenchymal stem cells in vitro.
J Cell Biochem 64:295-312.
16. Jansen JA, von Recum AF, van der Waerden JPCM, de
Groot K (1992) Soft tissue response to different types
of sintered metal fi bre-web materials. Biomaterials
13(13):959-968.
17. Johnson DL, McAllister TN, Frangos JA (1996) Fluid
fl ow stimulates rapid and continuous release of
nitric oxide in osteoblasts. Am J Physiol 271:E205-
208.
18. Kadiyala S, Young RG, Thiede MA, Bruder SP (1997)
Culture expanded canine mesenchymal stem cells
possess osteochondrogenic potential in vivo and in
vitro. Cell Transplant 6:125-134.
19. Klein-Nulend J, Burger EH, Semeins CM, Reisz LG,
Pilbeam CC (1997) Pulsating fl uid fl ow stimulates
prostaglandin release and inducible prostaglandin G/
H synthase mRNA expression in primary mouse bone
cells. J Bone Miner Res 12:45-51.
20. Lynch MP, Stein JL, Stein GS, Lian JB (1995) The infl u-
ence of type I collagen on the development and main-
tenance of the osteoblast phenotype in primary and
passaged rat calvarial osteoblasts: modifi cation of
expression of genes supporting cell growth, adhesion,
and extracellular matrix mineralization. Exp Cell Res
216:35-45.
References
1. Bakker AD, Soejima K, Klein-Nulend J, Burger EH
(2001) The production of nitric oxide and prostaglan-
din E(2) by primary bone cells is shear stress depen-
dent. J Biomech 34:671-677.
2. Bancroft GN, Sikavitsas VI, van den Dolder J, Sheffi eld
TL, Ambrose CG, Jansen JA, Mikos AG (2002) Fluid
fl ow increases mineralized matrix deposition in
three-dimensional perfusion culture of marrow
stromal osteoblasts in a dose-dependent manner.
PNAS 99:12600-12605.
3. Beck LS, Amento EP, Xu Y, Deguzman L, Lee WP,
Nguyen T, Gillett NA (1993) TGF- β 1 induces bone
closure of skull defects: temporal dynamics of
bone formation in defects exposed to rhTGF- β 1. J
Bone Miner Res 8:753-761.
4. Beck LS, Deguzman L, Lee WP, Xu Y, McFatridge
LA, Gillett NA, Amento EP (1991) TGF- β 1 induces
bone closure of skull defects. J Bone Miner Res
6:1257-1265.
5. Becker D, Geissler U, Hempel U, Bierbaum S,
Scharnweber D, Worch H, Wenzel KW (2002) Prolif-
eration and differentiation of rat calvarial osteoblasts
on type I collagen-coated titanium alloy. J Biomed
Mater Res 59:516-527.
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