1. Volume 60, Issue 4, Pages 1386-1396 (October 2001)
Expression of rat thick limb Na/H exchangers in potassium depletion and chronic metabolic acidosis 
Kamel Laghmani, Christine Richer, Pascale Borensztein, Michel Paillard, Marc Froissart, M.D., Ph.D 
Kidney International 
Volume 60, Issue 4, Pages (October 2001)
DOI: /j x
Copyright © 2001 International Society of Nephrology Terms and Conditions

2. Figure 1
Quantification of medullary thick ascending limb (MTAL) Na+/H+ exchanger-1 (NHE-1) mRNA by competitive reverse transcription-polymerase chain reaction (RT-PCR). (A) Ethidium bromide-stained gel for competitive RT-PCR analysis of 120ng MTAL total RNA. The amount of cRNA added in each reaction point was 0.36, 0.71, 1.43, 2.85, 5.7, 11.5, 23, 46 attomoles, from right to left, respectively, resulting in a progressive competition between PCR products derived from wild-type NHE-1 mRNA (lower band, 422 bp) and from cRNA (upper band, 541 bp). RT, reaction performed in the absence of reverse transcriptase (to rule out contaminating DNA). (B) Log-log plot of the ratio of quantitative fluorescence data expressed as a function of the initial amount of cRNA (attomoles). Ethidium bromide fluorescence of the PCR product obtained from cRNA was proportionally corrected to the difference in length observed with the PCR product amplified from the wild-type NHE-1 mRNA (corresponding to the 119bp insert). The log-log plot of the ratio of quantitative fluorescence versus initial amount of cRNA was drawn. Using this graphical representation, a particular ratio has to be pointed out when corrected fluorescences are equivalent. As the value of the ratio equals unit (log of the ratio is zero), the measured amount of wild NHE-1 mRNA is equal to the corresponding value on the horizontal axis (y = x ; r = 0.99).
Kidney International  , DOI: ( /j x)
Copyright © 2001 International Society of Nephrology Terms and Conditions

3. Figure 2
Quantification of MTAL NHE-1 mRNA (continued). (A) Relationships between NHE-1 mRNA quantified by competitive RT-PCR and total MTAL RNAs in the control group. Separate competitive RT-PCR were performed as described in the Methods section, using varying amounts of MTAL total RNA ranging from 50 to 350ng. The plot of NHE-1 mRNA abundance versus MTAL total RNA illustrates an excellent linearity over the total MTAL RNA range tested. (B) Typical dot-blot analysis of mRNAs in a case of acidosis versus control. Serial twofold dilutions of MTAL total RNA were submitted to dot-blot analysis, hybridized with 32P-labeled-oligo-dT as described in the Methods. After a one-hour exposure at -80°C, autoradiograms were digitized, and band densities were quantified. A representative autoradiogram of control (top) and acidosis (bottom) groups is shown. (C) Dot-blot densities are plotted against the amount of total RNA loaded per lane, and data are fitted by linear analysis. Results are expressed in blot density arbitrary units; no variation of total mRNA was discerned within the two experimental groups: (•) acidosis and (○) control.
Kidney International  , DOI: ( /j x)
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4. Figure 3
Effects of potassium depletion (KD) on MTAL NHE-1 mRNA. NHE-1 mRNA was analyzed by a competitive RT-PCR. Results are expressed in attomoles/μg of total RNA. (A) Two weeks of KD elicited a 48% increase for NHE-1 mRNA abundance. Each bar is mean (errors lines are ± SEM) out of four independent experiments. (B) After five weeks, KD no longer had an effect, as the level of NHE-1 mRNA in the depleted group returned to the control group value (N = 4).
Kidney International  , DOI: ( /j x)
Copyright © 2001 International Society of Nephrology Terms and Conditions

5. Figure 4
Effects of two and five weeks of potassium depletion (KD) on MTAL NHE-1 protein abundance. Immunoblots of membrane protein (30 μg/lane) are from MTAL suspensions from the control (C) and KD groups. (A) Immunoblots were obtained from two typical independent experiments in each condition. Membranes were probed with a polyclonal anti-NHE-1 antibody (1:300) as described earlier. The molecular weight standard is shown on the right. (B) Results obtained from four independent experiments in each condition are expressed as a function of the mean blot density value of the control group (normalized to 100%). A 93 and 89% increase was observed after two and five weeks of KD, respectively.
Kidney International  , DOI: ( /j x)
Copyright © 2001 International Society of Nephrology Terms and Conditions

6. Figure 5
Effects of NH4Cl administration on MTAL NHE-1 mRNA abundance. NHE-1 mRNA abundance was determined by competitive RT-PCR as described in the Methods section. Results are expressed in attomoles/μg of total RNA submitted in each point to the reaction. Each bar is the mean (errors lines are ±SEM) for six independent experiments. Metabolic acidosis did not induce any significant variation of NHE-1 mRNA.
Kidney International  , DOI: ( /j x)
Copyright © 2001 International Society of Nephrology Terms and Conditions

7. Figure 6
Effects of NH4Cl administration on MTAL NHE-1 protein abundance. Immunoblot of membranes protein (30 μg/lane) from MTAL suspensions of control (C) and acidosis (A) groups obtained from three typical independent experiments. Each experiment was performed twice on separate gels. Seven independent experiments did not elicit any significant effect of metabolic acidosis on NHE-1 protein abundance (+23%).
Kidney International  , DOI: ( /j x)
Copyright © 2001 International Society of Nephrology Terms and Conditions

8. Figure 7
Effects of potassium depletion (KD) on rat MTAL NHE-3 mRNA. NHE-3 mRNA competitive RT-PCR results are expressed in attomoles/μg of total RNA. Two weeks of KD had no effect on NHE-3 mRNA (A; N = 4). Conversely, at five weeks of KD, a 50% decrease in NHE-3 mRNA abundance was observed (B; N = 5).
Kidney International  , DOI: ( /j x)
Copyright © 2001 International Society of Nephrology Terms and Conditions

9. Figure 8
Effects of potassium depletion (KD) on rat MTAL NHE-3 protein abundance. Membranes were probed with a polyclonal anti-NHE-3 antibody (1:2500). The molecular weight standard is shown on the right. Each experiment was analyzed twice on separate gels. Conversely to the NHE-1 immunoblot results, neither two (A) or five weeks (B) of potassium depletion had an effect on the amount of NHE-3 protein.
Kidney International  , DOI: ( /j x)
Copyright © 2001 International Society of Nephrology Terms and Conditions