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. 2009 Aug 7;15(29):3611–3620. doi: 10.3748/wjg.15.3611

Table 1.

Phenotypic changes of donor-derived human cells in HRC liver during PHx-induced liver regeneration

Animal No. (age) Cell markers
AFP
CK19
CK18
CD34
CD45
I II I II I II I II I II
1 and 2 (2 mo) A - - + - - + - - - -
B - + + - - + - + - -
C - - + - - + - - - -
3 and 4 (2 mo) A - - + + + - + - - -
B - - + + + - + + - +
C - - + + + + - - - +
5 and 6 (2 mo) A - - + + + - - - - -
B - + + + + + - + - +
C - - + + + + - - - -
7 and 8 (2 mo) A - - - + + + - - - -
B - - - + + + - - - -
C - - - + + + - - - -
9 and 10 (2 mo) A - - - - + + - - - -
B - - - - + + - - - +
C - - - + + + - - - -

Animals 1-10 at the age of 2 mo with the engraftment of donor-derived hHLCs in the liver of HRC were screened by human gene-specific PCR for hAlu as previously described[19,20] and ISH for human Alu sequences confirmed by detecting human β2-M expression using IHC. Animals 2, 4, 6, 8 and 10 at the age of 2 mo underwent 70% PHx. Age-matched animals 1, 3, 5, 7 and 9 (not undergone PHx), were used as negative controls. In the human-rat chimeric liver, donor-derived human cells with different cellular phenotypes were detected by IHC for different markers (AFP, CD34, CD45, CK18 and CK19). Minimal liver tissues from PHx (II) and non-PHx (I) groups used for IHC were dissected and collected before PHx (A), and after 10 d (B) and 20 d (C) of PHx.