Expression of Tight Junction Molecule In The Human Serum-Induced Aggregation of Human Abdominal Adipose-Derived Stem Cells In Vitro
Previously we have shown that human abdominal adipose derived-stem cells (ADSCs) could aggregate during the high-density culture in the presence of human serum (HS). In the present study, we observed that human cord blood serum (CBS) and follicular fluid (HFF) also induced aggregation. Similarly, po...
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Veröffentlicht in: | Balsaeng'gwa saengsig 2014-12, Vol.18 (4), p.213-224 |
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Zusammenfassung: | Previously we have shown that human abdominal adipose derived-stem cells (ADSCs)
could aggregate during the high-density culture in the presence of human serum
(HS). In the present study, we observed that human cord blood serum (CBS) and
follicular fluid (HFF) also induced aggregation. Similarly, porcine serum could
induce aggregation whereas bovine and sheep sera induced little aggregation.
qRT-PCR analyses demonstrated that, compared to FBS-cultured ADSCs, HScultured
cells exhibited higher level of mRNA expression of
CLDN3, -6, -7,
-15
, and
-16
genes among the tight junction
proteins. ADSCs examined at the time of aggregation by culture with HS, BSA,
HFF, CBS, or porcine serum showed significantly higher level of mRNA expression
of
JAM2
among JAM family members. In contrast, cells cultured
in FBS, bovine serum or sheep serum, showed lower level of
JAM2
expression. Immunocytochemical analyses demonstrated that the aggregates of
HS-cultured cells (HS-Agg) showed intense staining against the anti-JAM2
antibody whereas neither non-aggregated cells (HS-Ex) nor FBS-cultured cells
exhibited weak staining. Western blot results showed that HS-Agg expressed JAM2
protein more prominently than HS-Ex and FBS-cultured cells, both of latter
reveled weaker intensity. These results suggest that the aggregation property of
ADSCs during high-density culture would be dependent on the specific components
of serum, and that JAM2 molecule could play a role in the animal sera-induced
aggregation
in vitro
. |
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ISSN: | 1226-6752 2465-9525 2287-7967 2465-9541 |
DOI: | 10.12717/DR.2014.18.4.213 |