posted on 2020-10-21, 12:04authored byWoo Sub Yang, Won Jin Kim, Ji Yeon Ahn, JiUn Lee, Dong Woo Ko, Sumin Park, Ji Yoon Kim, Chul Ho Jang, Jeong Mook Lim, Geun Hyung Kim
This study examined
whether neonatal chicken bone marrow cells (cBMCs) could support the
osteogenesis of human stromal cells in a three-dimensional (3D) extracellular
bioprinting niche. The majority (>95%) of 4-day-old cBMCs subcultured
5 times were positive for osteochondrogenesis-related genes (Col I, Col II, Col X,
aggrecan, Sox9, osterix, Bmp2, osteocalcin, Runx2, and osteopontin) and their related proteins (Sox9,
collagen type I, and collagen type II). LC–MS/MS analysis demonstrated
that cBMC-conditioned medium (c-medium) contained proteins related
to bone regeneration, such as periostin and members of the TGF-β
family. Next, a significant increase in osteogenesis was detected
in three human adipose tissue-derived stromal cell (hASC) lines, after
exposure to c-medium concentrates in 2D culture (p < 0.05). To evaluate biological function in a 3D environment,
we employed the cBMC-derived bioactive components as a cell-supporting
biomaterial in collagen bioink, which was printed to construct a 3D
hASC-laden scaffold for observing osteogenesis. Complete osteogenesis
was detected in vitro. Moreover, after transplantation of the hASC-laden
structure into rats, prominent bone formation was observed compared
with that in control rats receiving scaffold-free hASC transplantation.
These results demonstrated that substance(s) secreted by chick bone
marrow cells clearly activated the osteogenesis of hASCs in 2D- or
3D-niches.