Research Article

Acceleration of Functional Maturation and Differentiation of Neonatal Porcine Islet Cell Monolayers Shortly In Vitro Cocultured with Microencapsulated Sertoli Cells

Table 2

Immunohistochemical analysis of differentiation markers of NPI monolayers cultured alone or in the presence of ESC.

Cells (days)Ck7+/Insulin+ (%)PDX-1+/Insulin+ (%)Insulin+/c-kit+ (%)PDX-1/c-kit+ (%)

C (7)58.5 ± 1.414.8 ± 3.910.0 ± 1.713.1 ± 2.3
+ESC (7)55.3 ± 5.514.3 ± 3.09.7 ± 4.014.3 ± 9.7
C (14)50.0 ± 3.820.7 ± 3.114.0 ± 3.725.7 ± 10.0
+ESC (14)40.2 ± 2.433.3 ±   5.1*26.0 ±   0.9*31.1 ± 13.5
C (21)45.6 ± 4.729.5 ± 4.915.8 ± 2.945.1 ± 11.0
+ESC (21)32.9 ±   4.1*74.8 ±   4.9*38.3 ±   5.2*71.8 ±   10.8*

C: Control untreated NPI monolayers.
+ESC: NPI monolayers cocultured in the presence of encapsulated Sertoli cells.
Data represent the percentage of positive cells and are given as means ± SD (n = 3).
*P < .050.