c-myc antisense oligonucleotide treatment ameliorates murine ARPKD

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c-myc antisense oligonucleotide treatment ameliorates murine ARPKD Justin L. Ricker, John E. Mata, Patrick L. Iversen, Vincent H. Gattone  Kidney International  Volume 61, Issue 1, Pages S125-S131 (January 2002) DOI: 10.1046/j.1523-1755.2002.0610s1125.x Copyright © 2002 International Society of Nephrology Terms and Conditions

Figure 1 Light micrographs of 20 day-old control andc-mycASO treated C57BL/6J-cpkcystic kidneys. Compared with (a, b) control cystic kidney, (c, d) c-myc ASO treated cystic kidney exhibits an increased amount of normal renal parenchyma. a, b: 8X; c, d: 30X. Kidney International 2002 61, S125-S131DOI: (10.1046/j.1523-1755.2002.0610s1125.x) Copyright © 2002 International Society of Nephrology Terms and Conditions

Figure 2 Renal mRNA expression in 20 day-old control, scrambled oligonucleotide andc-mycASO treated normal and cystic C57BL/6J-cpkmice. The c-myc, histone H4, and SGP-2 messages were overexpressed in cystic compared to normal kidney. c-myc ASO treatment did not alter c-myc or histone H4 mRNA expression, but did decrease SGP-2 mRNA expression nearly 40% in cystic kidney. EGF mRNA was severely diminished in cystic compared to normal kidney, but was increased 12-fold in cystic kidney following c-myc ASO treatment. All of the northern blot hybridization studies were performed in duplicate using different sets of RNAs. Representative autoradiographs as well as methylene blue staining of 28S and 18S ribosomal RNA to ensure equal loading and transfer of RNA are shown. Kidney International 2002 61, S125-S131DOI: (10.1046/j.1523-1755.2002.0610s1125.x) Copyright © 2002 International Society of Nephrology Terms and Conditions

Figure 3 Western blot analysis in 20 day-old control andc-mycASO treated C57BL/6J-cpkcystic kidney. The c-Myc and PCNA protein levels were reduced 59% and 30%, respectively, in cystic kidney following c-myc ASO treatment. All of the western blot hybridization studies were performed in duplicate using different sets of total renal protein samples. Glucocorticoid receptor was used as a control for loading (based on unpublished data from R. Maser, personal communication). Kidney International 2002 61, S125-S131DOI: (10.1046/j.1523-1755.2002.0610s1125.x) Copyright © 2002 International Society of Nephrology Terms and Conditions

Figure 4 Localization of c-Myc protein in 20 day-old control andc-mycASO treated C57BL/6J-cpkcystic kidney. (a, b) c-Myc protein is localized to the nuclei of epithelial cells lining cystic (arrowheads) and noncystic (*) tubules in control cystic kidney. (c) After c-myc ASO treatment, the c-Myc protein is reduced in the nuclei of epithelial cells lining the noncystic tubules, but unchanged in cystic tubules. a: 100X; b, c: 400X. Kidney International 2002 61, S125-S131DOI: (10.1046/j.1523-1755.2002.0610s1125.x) Copyright © 2002 International Society of Nephrology Terms and Conditions