Immunofluorescent staining and miRNA expression of HCT-8 AND HT-29 cell lines upon Cryptosporidium infection
The protozoan Cryptosporidium mainly infects the epithelial cells of colorectal region. The Infection of this species can be observed and confirmed by immunofluorescent staining method in vitro. Meanwhile, the onco-microRNA and tumour suppressor miRNA expression pattern of the epithelial cells upon...
| Main Authors: | , , |
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| Format: | Conference or Workshop Item |
| Language: | English |
| Published: |
2018
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| Subjects: | |
| Online Access: | http://irep.iium.edu.my/67087/ http://irep.iium.edu.my/67087/1/Abstract%20MSAB%20conference-%20Jainul%20et%20al.pdf |
| Summary: | The protozoan Cryptosporidium mainly infects the epithelial cells of colorectal region. The Infection of this species can be observed and confirmed by immunofluorescent staining method in vitro. Meanwhile, the onco-microRNA and tumour suppressor miRNA expression pattern of the epithelial cells upon Cryptosporidium infection may reveal possible effect of Cryptosporidium in the onset and progression of cancer. In this study, two epithelial colorectal cancer cell lines HCT8 and HT29 were infected with Cryptosporidium parvum (C. parvum) and observed using direct immunofluorescent technique via fluorescein conjugated Vicia Villosa Lectin (VVL) staining. Then, the RT-qPCR was performed to observe the expression of miR-21 and miR-145 in infected cell lines. Data normalization of the miRNA expression was carried out using reference gene RNU44. The immunofluorescent micrographs exhibited the Cryptosporidium infection on both HCT-8 and HT-29 cell lines with green fluorescence. Upregulation of miR-21 and downregulation of normalized expression of miR-145 was observed in both of the cell lines upon Cryptosporidium infection. We found the expression of miR-21 to be increased and miR-145 greatly decreased in both cell lines upon infection. Our current observation suggests that, C. parvum can potentially infect the colorectal cancer cell lines and play critical role in regulating oncomiRNAs and tumor suppressor miRNAs. |
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