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Letter to the editor: “Quantifying albumin permeability with multiphoton microscopy: why the difference?”

2014; American Physical Society; Volume: 306; Issue: 9 Linguagem: Inglês

10.1152/ajprenal.00652.2013

1931-857X

Ruben M. Sandoval, Bruce A. Molitoris,

Monoclonal and Polyclonal Antibodies Research

Letters to the EditorLetter to the editor: “Quantifying albumin permeability with multiphoton microscopy: why the difference?”Ruben M. Sandoval, and Bruce A. MolitorisRuben M. SandovalIndiana University School of Medicine and Indiana Center for Biological Microscopy and Roudebush Veterans Affairs Medical Center, Indianapolis, Indiana, and Bruce A. MolitorisIndiana University School of Medicine and Indiana Center for Biological Microscopy and Roudebush Veterans Affairs Medical Center, Indianapolis, IndianaPublished Online:01 May 2014https://doi.org/10.1152/ajprenal.00652.2013MoreSectionsPDF (398 KB)Download PDF ToolsExport citationAdd to favoritesGet permissionsTrack citations to the editor: Utilizing intravital multiphoton microscopy, Schießl and Castrop (19) examined glomerular albumin permeability and the effect of angiotensin II. Recent data relating to glomerular albumin permeability and proximal tubule cell albumin handling have renewed the debate regarding the importance of both facets in albuminuria. The utilization of multiphoton microscopy to study this phenomenon has divided the community as initial studies by Russo et al. (13) reported a glomerular sieving coefficient for albumin (GSCA) ∼50× greater than previously reported by techniques such as micropuncture (23). The model generated by these higher glomerular albumin permeability values relies on reabsorption and transcytosis of albumin and is gaining traction as numerous investigators have delineated proximal tubule (PT) proteins whose dysfunction results in albuminuria (5, 11, 18). Notably, three different investigators using diphtheria toxin receptor insertion into PT cells showed PT injury lead to a marked increase in albuminuria with normal glomerular light and electron microscopy morphology (5, 20, 25). In particular, Sekine et al. (20) (Fig. 3), Zhang et al. (25) (Fig. S4), and the review by Grgic et al. (5) (Fig. S4) show marked proteinuria and albuminuria, well into the nephrotic range, occurring temporally with PT dysfunction following one treatment with diphtheria toxin, and disappearing with PT recovery. There were no changes in glomerular morphology at either the light (25) or electron microscopic (5) levels.Publications by Peti-Peterdi and Tanner in 2009 (10, 21), which were referenced by Scheiβl and Castrop (19), sowed doubt and confusion about the GSCA values reported by Russo et al. (12, 13). Briefly, Peti-Peterdi reported a low GSCA value that was not measured using albumin but by a broadly dispersed 70-kDa rhodamine dextran (10). On closer inspection, this dextran generated a time-dependent GSC as the smaller molecular weight (MW) fractions were cleared out early, leaving larger MW fractions to produce increasingly lower GSCs (16). In the second study conducted by Russo et al. (12), molecular calibration using a narrowly dispersed 69.7-kDa dextran produced a GSC values of 0.025 ± 0.0041, virtually identical to those obtained by Rippe's group using fractional clearance for the same sized dextran with similar dispersion characteristics (0.022) (1).Schieβl and Castrop also cite Tanner's editorial (21) that attributed Russo's high-albumin GSCA to an out-of-focus fluorescence contributing signal into Bowman's space when using external (nondescanned) detectors and poor physiological preparations. However, Peti-Peterdi in all his studies (8, 10, 14) and Scheiβl and Castrop (19) used external (nondescanned) and generated very low GSCA numbers. This rules out implicating out-of-focus fluorescence emanating from the use of external detectors as the reason for our higher GSCA. Typically, out-of-focus fluorescence emission is not a problem with two-photon excitation due to the physics of the light generation at the point of excitation (2, 16). However, Theer and Denk (22) describe how out-of-focus fluorescence can become a problem at very deep imaging depths (+900 μm). Measurements made in the kidney for our studies are acquired at depths of 15–25 μm, so this is not a concern. Finally the use of internal detectors, compared with external nondescanned detectors, was shown (16) to decrease sensitivity, partially explaining the reported reduction in GSC. Numerous manuscripts from our laboratory (12, 13, 15–17) challenged Tanner's editorial, citing poor physiological preparations because our techniques are consistent, multiple parameters are measured and controlled, and values remain virtually identical between studies. In a paper by Comper and Russo (4), the GSCA for individual glomeruli remained time independent for the 90 min they were observed. Moreover, other studies done in collaboration with Tanner, using the same techniques, resulted in stable physiological parameters for several hours (3, 6, 7).We believe the lack of agreement within published multiphoton data regarding GSCA is primarily due to factors affecting sensitivity in digital microscope systems that are not widely known or utilized (9). Our study on the effects of photodetector offset provides extensive characterization both in vitro and in vivo and was carried out using gradually increasing offset values (17). This lowers the system's ability to detect low-intensity values, thus minimizing signal recording. In our study, in vitro sensitivity calibration curves using a series of fluorescent albumin concentrations revealed a marked decrease in detector sensitivity with progressively increasing offsets in which more and more pixel values in the image are forced to zero. In in vivo studies looking at GSCA with the same series of offsets in identical glomeruli, the average GSC dropped from a peak 0.0152 ± 0.0047 for offset 38 (typically used in our studies), to 0.00017 ± 0.00003 for offset 52, where background values are essentially zero (see Fig. 1). In studies by Nakano et al. (8), they adjusted the detector offset for each individual glomerulus pre- and postinfusion of albumin to a lower background. For quantitative imaging, the offset is set once and should not be adjusted for the duration of the experiment (9, 24). Nakano et al. (8) may have done this in an effort to force tissue autofluorescence intensities to fall within those of electronic noise or even cell culture autofluorescence. However, intravital tissues are rich in naturally occurring autofluorescent structures, and adjusting the offset to force the fluorescence of these structures to zero results in a marked decrease in sensitivity, thus minimizing albumin detection as we have documented (17).Fig. 1.Photodetector offset influences glomerular albumin permeability values dramatically. The offset or “black level” settings determines the lower detection limits on the photomuliplier tube (PMT) detectors found in many laser scanning confocal and multi-photon microscopes. A: effect on detector sensitivity using 2 different offsets on a range of background subtracted Texas red albumin (TRA) solutions in vitro. The average intensity readings from the images were divided by the concentration of TRA to give a direct unit of sensitivity. This unit should be constant across the concentration range if sensitivity is unaffected, as shown when offset is set to 38. Using a higher numerical offset of 45, which forces background values closer to zero, markedly decreases the microscope's ability to correctly detect fluorescence in identical dishes. With detector sensitivity decreased particularly at lower TRA concentrations, the sensitivity value is no longer constant across the range for offset 45. B: list of background subtracted, glomerular sieving coefficients for albumin (GSCA) collected at different offsets for the same set of glomeruli. Note the rapidly decreasing GSCA seen starting at offset 42. There is a 262-fold decrease in GSCA in a comparison of offsets 38 and 52. C and D: identical images of a glomerulus after infusion of TRA, taken at offsets 38 and 45, respectively. The blue color seen in Bowman's space in D (offset 45) indicates the values located therein have a value of zero before background subtraction. Colors alerting the user to pixels in the image having intensity values above or below the detection limit of the detectors are standard in every microscope system (typically red for saturated values and blue or green for values at zero). The GSC for TRA in these experiments, where only the offset was changed for the image, averaged 0.015 ± 0.0047 using offset 38 and 0.00114 ± 0.00096 using offset 45. Values in this, and all of our studies, were background subtracted, with a reference image taken at the corresponding offsets.Download figureDownload PowerPointThe current work of Schieβl and Castrop (19) appears to have used settings causing this same lack of sensitivity produced when using higher offsets. Evaluation of a digital copy of Fig. 1B from their manuscript when it was downloaded, color decoded, blue channel selected, and thresholding was done of the corresponding blue region of the glomerulus revealed ∼87.3% of the pixels had a reading of zero. This would correspond to an offset of 42–45 in our study (17). This places the sensitivity well below the linear range for filtered albumin in an extrapolation to our study. (Note: the blue color warns the user the highlighted pixels have an intensity value of zero). To correctly adjust the offset, one should instead generate a “pre-” background image before infusion of a fluorescent compound and use those images to subtract the background values from identical image planes and regions taken postinfusion (15). The offsets should be set so that only a few pixels randomly display a value of zero (blue) and are not adjusted further. Indeed, factors critical in measuring GSCA were validated in our two previous studies (16, 17). Nuances in novel technologies such as the correct photodetector offset, critical in multiphoton microscopy, can lead to generation of erroneous data when inappropriately set. These parameters are not widely understood and must be identified and better established in future studies.DISCLOSURESNo conflicts of interest, financial or otherwise, ad declared by the authors.AUTHOR CONTRIBUTIONSR.M.S. and B.A.M. drafted the manuscript; R.M.S. and B.A.M. prepared figures; R.M.S. and B.A.M. edited the manuscript; R.M.S. and B.A.M. revised the manuscript; R.M.S. and B.A.M. approved the final version of the manuscript.REFERENCES1. Asgeirsson D, Venturoli D, Fries E, Rippe B, Rippe C. Glomerular sieving of three neutral polysaccharides, polyethylene oxide and bikunin in rat. Effects of molecular size and conformation. Acta Physiol 191: 237–246, 2007.Crossref | PubMed | ISI | Google Scholar2. Centonze VE, White JG. Multiphoton excitation provides optical sections from deeper within scattering specimens than confocal imaging. Biophys J 75: 2015–2024, 1998.Crossref | PubMed | ISI | Google Scholar3. Choong FX, Sandoval RM, Molitoris BA, Richter-Dahlfors A. 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Piston1 May 2014 | American Journal of Physiology-Renal Physiology, Vol. 306, No. 9 More from this issue > Volume 306Issue 9May 2014Pages F1098-F1100 Copyright & PermissionsCopyright © 2014 the American Physiological Societyhttps://doi.org/10.1152/ajprenal.00652.2013PubMed24785957History Published online 1 May 2014 Published in print 1 May 2014 Metrics