Distribution and expression of nephrin,podocin and α-actinin in a conditionally immortalized mouse podocyte cell line
Na Guan
Abstract
Na Guan
Abstract
Objective: To analyze the distribution and expression of nephrin, podocin and a-actinin in a conditionally immortalized mouse podocyte cell line (MPC 5), which will be in vitro model for studying the relationship among podocyte molecules. Methodology: MPC 5 were induced to propagate and passage by γ-inferon at 33℃, which were subsequently cultured at 37℃ for differentiation for two weeks. The podocyte morphology was observed by phase-contrast microscope. The distribution of nephrin, podocin and α-actinin was revealed by immunofluorescence (IF) staining. Results: ① In the light microscopy, differentiated cells presented with the polygoneal shape and with the formation of processes. ② IF the staining of nephrin and podcin was mainly distributed on the surface of cellular membrane in a filamentous pattern. The staining of α-actinin was specifically localized to the nuclear. ③ Expressions of nephrin, podocin and α-actinin mRNAs in MPC 5 were detected by RT-PCR. ④ Expression of nephrin, podocin, α-actinin and WT1 in MPC 5 were shown by Western blotting with the size of approximately 180 KDα, 45 kdα, 100 KDα and 52 KDα, respectively. Conclusion: For the first time, we demonstrated the expression of nephrin, podocin and α-actinin both at mRNA level and at protein level in mouse MPC 5.
A significance statement is not available in the OpenAlex record.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Objective: To analyze the distribution and expression of nephrin, podocin and a-actinin in a conditionally immortalized mouse podocyte cell line (MPC 5), which will be in vitro model for studying the relationship among podocyte molecules. Methodology: MPC 5 were induced to propagate and passage by γ-inferon at 33℃, which were subsequently cultured at 37℃ for differentiation for two weeks. The podocyte morphology was observed by phase-contrast microscope. The distribution of nephrin, podocin and α-actinin was revealed by immunofluorescence (IF) staining. Results: ① In the light microscopy, differentiated cells presented with the polygoneal shape and with the formation of processes. ② IF the staining of nephrin and podcin was mainly distributed on the surface of cellular membrane in a filamentous pattern. The staining of α-actinin was specifically localized to the nuclear. ③ Expressions of nephrin, podocin and α-actinin mRNAs in MPC 5 were detected by RT-PCR. ④ Expression of nephrin, podocin, α-actinin and WT1 in MPC 5 were shown by Western blotting with the size of approximately 180 KDα, 45 kdα, 100 KDα and 52 KDα, respectively. Conclusion: For the first time, we demonstrated the expression of nephrin, podocin and α-actinin both at mRNA level and at protein level in mouse MPC 5.
Key concepts: Podocin, Nephrin, Podocyte, Cell biology, Blot, Biology, Molecular biology, Chemistry