Cyto-histopathological and protein polymorphism alterations in five populations of Nile tilapia (Oreochromis niloticus) as biomonitor for water heavy metal pollution.

Cytological, histopathological and sodium dodecyl sulphate polyacrylamide gel analyses were carried out on five populations of common Nile tilapia fish (Oreochromis niloticus) occurring in five sites - River Nile (reference site), Bahr Yusef canal, Ibrahimia canal, Irrigation drain and El Moheet drain of El Minia Province, Egypt - to evaluate the usability of Nile tilapia as a biomonitor for water heavy metal contaminants. Water surface samples were collected from the five sites, and lead (Pb) concentration was shown to surpass the limits defined by WHO. Ni and Cd levels were shown to be elevated in Ibrahimia canal samples. Moreover, the concentration of heavy metals in fish muscles collected from Bahr Yusef canal and El Moheet drain was the highest in comparison with those of the other water sites. Cytological examinations of blood smears showed not only a significant percentage of micronuclei in Irrigation drain population but also a significant percentage of binucleated cells in Ibrahimia canal and El Moheet drain populations. In addition, pathological alteration was observed in blood cells, especially in samples collected from Irrigation drain and El Moheet drain. Histopathological changes were strongly observed in the liver and the kidneys of El Moheet and Irrigation drain population. Moreover, total protein band pattern profiles showed extra bands in both Ibrahimia canal and Irrigation drain more than that recorded for the River Nile population. In conclusion, cyto-histopathological and total protein band pattern results confirmed that O. niloticus responds sensitively to the excess of heavy metals present in the water.

Cleavage of growth differentiation factor 15 (GDF15) by membrane type 1-matrix metalloproteinase abrogates GDF15-mediated suppression of tumor cell growth.

Growth differentiation factor 15 (GDF15), a transforming growth factor (TGF)-beta superfamily member, has been cloned from a placenta cDNA library as a gene product that has promoted activation of pro-matrix metalloproteinase (MMP)2 mediated by membrane type (MT)1-MMP. Expression of MT1-MMP in HEK293T cells caused cleavage of the GDF15 mature form at N(252)-M(253) to produce a 6-kDa C-terminal fragment. Treatment of MCF7 cells with GDF15 induced activation of p53 and enhanced expression of p21, which was abrogated by MT1-MMP expression. GDF15 mRNA synthesis was also shown to be induced by treatment of cells with GDF15. Treatment of MCF7 cells with GDF15 caused suppression of cell proliferation. However, proliferation of MCF7 cells transfected with the MT1-MMP gene was not affected by GDF15 treatment, but was suppressed in the presence of the MMP inhibitor BB94. HT1080 cells transfected with the GDF15 gene, which endogenously express MT1-MMP, synthesize a high-level GDF15 precursor form and a low-level mature form, and treatment of cells with BB94 enhanced production of the GDF15 mature form. Consistent with GDF15 production, HT1080 cells transfected with the GDF15 gene proliferated almost equally with control cells, and addition of BB94 effectively suppressed growth of HT1080 cells transfected with the GDF15 gene concomitant with the accumulation of the GDF15 mature form, but not control cells. These results suggest that MT1-MMP contributes to tumor cell proliferation through the cleavage of GDF15, which down-regulates cell proliferation by inducing activation of p53 and p21 synthesis.