Chinese Medicine Vol.06 No.01(2015), Article ID:54148,6 pages
10.4236/cm.2015.61002
miRNAs Expression and Role of Dicer on Podocyte Injury in PAN Nephrosis Rats
Chunqing Li1,2, Wei Sun2,3*, Haochang Du1, Dong Zhou3, Jihong Chen3, Lu Zhang3, Jiade Shao3
1Nephrology Department of Wuxi No. 3 Hospital, Wuxi, China
2Discipline of Chinese and Western Integrative Medicine, Nanjing University of Chinese Medicine, Nanjing, China
3Nephrology Department of Jiangsu Province Hospital of Traditional Chinese Medicine, Nanjing, China
Email: *jssunwei@163.com
Copyright © 2015 by authors and Scientific Research Publishing Inc.
This work is licensed under the Creative Commons Attribution International License (CC BY).
http://creativecommons.org/licenses/by/4.0/
Received 1 January 2015; accepted 12 February 2015; published 16 February 2015
ABSTRACT
Objective: microRNAs (miRNAs) are regulatory RNAs that act as important players
in diverse biologic and pathologic processes. Under circumstance as podocye-injury
triggering proteinuria, which miRNAs are up-regulated or down-regulated? This experiment
aims at detecting miRNAs changes in PAN nephrosis rats based on miRNA arrays and
exploring the therapeutic targets of Leizhi capsule. Methods: Fifty male wistar
rats were randomly divided into five groups, including control group, model group,
leizhi capsule group, Tripterygium glucosides group, and valsartan group. PAN nephrosis
models were made by jugular vein injection of PAN (100 mg/kg body weight, dissolve
in physiological saline), while control group rats were made by jugular vein injection
of physiological saline with equal volume. Other groups rats had been given medicines
by irrigating stomach once a day for ten days. Blood and urine samples were collected,
and renal tissues were processed after rats being euthanasised. The 24 h urinary
protein excretion and blood biochemistry parameters were measured by routine methods.
The glomerular morphology and podocyte ultrastructure were observed with light microscopy
and transmission electron microscopy respectively. miRNA expression profile was
detected by Exiqon miRNA Array. Real time RT-PCR analysis for mature miRNAs was
used to validate differentially expressed miRNAs. Results: 1) In day 3 - 5, model
rats had decreased urine volume, ascites, malnutrition and wight loss. From day
7 to day 10, the nephrotic syndromes were worst in model rats, but which had no
skin edema. Some rats died in serious ascites, the mortality is 3/10. 2) miRNA array
detection shows 106 miRNAs up regulated and 62 miRNAs down regulated in PAN nephrosis
rats. Fold change (model vs. control group) varies from 1.8 to 7.0. For leizhi capsule
group and model sample, there are 90 miRNAs differentially expressed, with 65 miRNAs
up and 25 miRNAs down. The most important finding in our research is the discovery
of the specific miRNAs related to PAN nephrosis (rno-miR
Keywords:
microRNAs, Podocyte Injury, Puromycin Aminonucleoside Nephrosis Model, Proteinuria, Leizhi Capsule
1. Introduction
microRNAs (miRNA) are a group of non-coding small RNA (approximately 22-nt) that are present in lower through higher organism and function to regulate gene expression by translation repression or transcript degradation of target genes. Dicer is a key enzyme in miRNA biosynthetic, by which pri-miRNAs are processed into approximately 22-nt mature microRNA [1] [2] . In addition, Dicer is involved in the immediate downstream effecter steps of this pathway, whereby it serves as an essential component of miRNA-containing catalytic enzyme complexes, such as the RNA-induced silencing complex. Thus, as a physical platform and a functional bridge, Dicer couples miRNA biogenesis to miRNA-mediated gene silence [3] .
Proteinuria is a dangerous factor of chronic kidney disease (CKD). Podocyte injury is not only the key link of proteinuria, but also closely contacts with CKD progress. Some microRNAs may induce slit diaphragm (SD) molecules expression via triggering nephrin phosphorylation to reduce proteinuria [4] -[6] . As a key enzyme of miRNA biosynthesis, dicer probabaly have a role on proteinuria of CKD. Podocyte-selective deletion of dicer induces proteinuria and glomerulosclerosis [1] [7] , also alter cytoskeletal dynamics and causes glomerular disease [1] [2] [8] , leading to rapid glomerular and tubular injury [3] [9] . It is suggested that dicer and these miRNAs are probably key regulated targets. How dicer enzyme have effects on podocyte in PAN (puromycin aminonucleoside, PAN) nephrosis pathlogy? So the aim of our experiment is to explore how dicer has effects on podocyte apotosis and cytoskeleton.
2. Methods
Fifty male Wistar rats were divided into five groups, including: 1) control group, 2) PAN model group, 3) leizhi group, 4) Tripterygium glucosides (GTW) group, and 5) valsartan group.
PAN model rats were made by jugularly intravenous injecting with PAN (100 mg/kg) [10] , while control group rats were made by intravenous injecting with physiological saline. After injection, all rats were feeding with clear water and food for ten days in metabolic cage.
By irrigation stomach once a day for ten days, all rats had been given medicines as follows:
1) Physiological saline (2 ml) for control group and model group;
2) Tripterygium glucosides (2 mg) dissolved in Erzhi (containing Ligustrum lucidum and Drought Ephraim grass) solusion (1 ml) for Leizhi group;
3) Tripterygium glucosides 1 mg/kg/d for Tripterygium glucosides group;
4) Triptolid 2 mg/200g/d for triptolid group ;
5) Valsartan valsartan 1.5 mg/200g/d for valsartan group.
Urine was collected on alternate day, and blood sample were gathered before and after experiment. After all rats being euthanasised, kidneys and livers were removed for Electron microscopy, Immunofluorescence stain and RT-PCR and western bloting.
miRNA Array analysis has been accomplished by Shanghai KangChen Biological engineering company. miRNA expression profile was detected by Exiqon miRNA Array, including: prepare the RNA Sample and RNA Sample QC, miRNA labeling, miRNA array hybridization, miRNA array scanning and analysis. Real time RT-PCR analysis for mature miRNAs was used to validate 4 differentially expressed miRNAs between control and model group in microRNA microarray assays.
3. Results
PAN nephrosis rats were made successfully by jugular vein injection of PAN (100 mg/kg body weight). In day 5, model rats were in low spirits, with decreased urine volume, ascites, malnutrition and weight loss. From day 7 to day 10, proteinueia for 24 h were worst in PAN model rats, but without skin edema, see Table 1. Some rats died of serious ascites, the mortality is 30% (3/10).
Morphologic changes in light microscope include epithelial cells degeneration renal tubular and transparent cast, but there are no obvious changes in glomerulus and renal interstitial. Podocyte processes effacement was obvious in model groups sample in electronic microscope. See in Figure 1.
miRNA array detection shows 106 miRNA up regulated and 62 miRNA down regulated in PAN nephrosis rats. Fold change (model vs. control group) vary from 1.8 to 7.0. For leizhi capsule high-dose group and model sample, there are 90 miRNA differentially expressed, with 65 up and 25 down. see Figure 2 and Figure 3.
The most important finding in our study is the discovery of the specific miRNA related
to PAN nephrosis (rno-miR
Compared with control sample, Immune Fluorescence intensity of nephrin, podocin and synaptopodin reduced in model sample. See in Figure 3. In addition, apoptosised podocytes increase in PAN sample.
Table 1. Proteinuria for 24 h among each group.
Compared with NS group, 1)representing p < 0.05, compared with PNS group, 2)representing p < 0.05, compared with Leizhi group, 3)representing p < 0.05.
Table 2. miRNAs expression by miRNA Array and realtime RT PCR. (a) miRNA expression (model versus NS). (b) miRNA expression (leizhi versus PAN).
(a)(b)(c)(d)
Figure 1. Change of foot process of glomerular podocyte in PAN rats. (a) NS, (b) PAN, (c) Leizhi, (d) GTW (8000×).
(a) (b)
Figure 2. Differentially expressed miRNAs screening by miRNA Arrays. (a) Up-expressed miRNAs; (b) Down-expressed miRNAs.
Figure 3. Immunoflunce of dicer, nephrin, podocin, and synodopotoptin in glomerular. (a) NS, (b) PAN, (c) Leizhi, (d) GTW.
4. Discussion
PAN nephrosis rats can be made successfully by jugular vein injection of PAN. PAN can selectively injury podocytes but not mesangium or endothelial cells in glomerular, inducing proteinuria, foot process effacement, and glomerular basement membrane abnormalities. So PAN nephrosis has been a classic podocyte-injury model.
Dicer is key to miRNA mature, which can mentain podocyte function and structure
of SD in kidney. Our results show that dicer correlates well with proteinuria, but
correlating negatively with nephrin and podocin. The most important finding in our
study is the specific miRNA related to PAN nephrosis (rno-miR
Dicer can be down-regulated in PAN induced rats treated with Tripterygium preparation.
Expression profile of nephrin, podocin and synaptopodin mRNA and protein decrease
in samples treated with Tripterygium wilfordii Hook by triggering dicer-miRNA, which
play the podocyte protection role by inhibiting podocyte apotosis. So these miRNAs
(rno-miR-24, rno-miR-30c, rno-miR
From our work, we can conclude that characteristic miRNAs of PAN nephrosis were
screening. Up-regulated miRNAs (rno-miR-23a, rno-miR-300-3p) may trigger podocyte
injury and proteinuria, while down-regulated miRNAs (rno-miR-24, rno-miR
Acknowledgements
miRNA Array analysis has been accomplished by Shanghai Kang Chen Biological engineering company.
Financial Support
The experiment is funded by Jiangsu province natural science fund (BK2009462) and the Priority Academic Program Development of Jiangsu Higher Education Institutions (PAPD).
Conflict of Interest Statement
The authors declare no conflicts of interest.
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NOTES
*Corresponding author.