The use of bioresorbable conduits supplemented with Schwann cells (SCs) is
a promising tissue engineering technique to replace nerve grafting. Alginat
e hydrogel (AH), as a SC tissue engineering matrix, has many advantages ove
r previously used matrices but has not been evaluated for this purpose. In
this study, the viability and proliferation of SCs together with SC functio
n in AH was evaluated in vitro. AlamarBlue(TM) cell assay was used to monit
or the viability of SCs in AH and compared to SC viability in collagen gel,
fibrin glue, hyaluronic acid, Matrigel(R), and standard culture plate over
5 days in culture. The results showed that the viability and growth of SCs
in different matrices over the culture period did not significantly differ
to culture plate culture. SC function when suspended in AH was monitored u
sing chick embryo dorsal root ganglia (CDRG) growth assay. Growth of CDRG i
n AH with or without SCs was compared to CDRG growth without AH matrix. Aft
er 3 days in culture, the mean length of neurite sprouting was measured. Th
e results showed that there was neurite growth in AH but was reduced to 43%
of control. The neurite growth in AH was, however, enhanced by 170% when S
Cs were suspended in the gel. In conclusion, AH supported SC viability and
function in vitro and may be useful in peripheral nerve tissue engineering
in reconstructive procedures.