Molecular Vision 2013; 19:1290-1295
<http://www.molvis.org/molvis/v19/1290>
Received 24 January 2013 | Accepted 07 June 2013 | Published 11 June 2013
Molecular Vision 2013; 19:1290-1295
<http://www.molvis.org/molvis/v19/1290>
Received 24 January 2013 |
Accepted 07 June 2013 |
Published 11 June 2013
Byung-Jin Kim,1 Nicholas Sprehe,2 Ashley Morganti,2 Robert J. Wordinger,1 Abbot F. Clark1
1Department of Cell Biology & Anatomy and The North Texas Eye Research Institute, University of North Texas Health Science Center, Fort Worth, TX; 2Lions Eye Institute for Transplant and Research, Tampa, FL
Correspondence to: Abbot F. Clark, Department of Cell Biology and Anatomy, NTERI/CBH-441, University of North Texas Health Science Center, 3500 Camp Bowie Boulevard, Fort Worth, TX, 76107; Phone: (817) 735-2094; FAX: (817) 735-2637; email: Abe.Clark@unthsc.edu
Purpose: Profiling gene expression in human ocular tissues provides invaluable information for understanding ocular biology and investigating numerous ocular diseases. Accurate measurement of gene expression requires high-quality RNA, which often is a challenge with postmortem ocular tissues.
Methods: We examined the effect of various death to preservation (DP) times on the RNA quality of ten different ocular tissues. We used 16 eyes from eight different human donors. The eyes were preserved immediately in RNAlater or preserved after initial storage at 4 °C to create a range of DP times from 2 to 48 h. Ten ocular tissues were dissected from each eye. After total RNA was extracted from each dissected ocular tissue, the RNA integrity number (RIN) was determined using an Agilent Bioanalyzer.
Results: The RIN values from corneal and trabecular meshwork tissues were significantly (p<0.05) higher than those from the ciliary body at an earlier DP time (<6 h), but were not different among all tissues after 8 h. Interestingly, the RIN values from non-vascularized tissues were significantly (p=0.0002) higher than those from vascularized ocular tissues at early DP times (<6 h). The RIN value from the cornea was significantly (p<0.05) higher at short DP times compared to longer DP times. The RIN values from corneal tissues were significantly correlated to DP time according to regression analysis (p<0.05).
Conclusions: In this study, we determined RNA quality from postmortem ocular tissues with various DP times. Our results emphasize the need for rapid preservation and processing of postmortem human donor eye tissues, especially for vascularized ocular tissues.
Messenger ribonucleic acid (mRNA) mediates informational transfer from genomic DNA to biologic effector protein molecules. Gene expression profiling using RNA isolated from cells and tissues has been extensively used to study the development, differentiation, and effects of exogenous factors such as growth factors and drugs, as well as to better understand disease pathogenesis. Although isolating RNA from fresh cell cultures is relatively straightforward, harvesting RNA from tissues, particularly human tissues, is more challenging. RNA integrity in tissues depends on the postmortem time to preservation, the metabolic profiles of the tissues, endogenous RNase activity, and natural RNA degradation.
Numerous studies have been performed to study mRNA expression profiles using various techniques, including reverse transcription–polymerase chain reaction (RT–PCR), RNA differential display, DNA microarrays, and RNAseq. In particular, microarray analysis of mRNA expression has been used to identify genes associated with aging [1], retinal stem/progenitor cell biology [2], as well as the pathophysiology of certain diseases such as age-related macular disease (AMD) [3], rod-cone dystrophy [4], retinitis pigmentosa (RP) [5], and glaucoma [6]. DNA microarrays have been used to profile genome-wide gene expression in multiple human ocular tissues to investigate the physiology and pathophysiology of the eye [7]. However, several obstacles exist to obtaining high-quality RNA from human donor eyes.
RNA is progressively degraded in postmortem tissues and during RNA extraction. In many cases, RNA extracted from donor eye tissues is not of optimal quality, which complicates gene expression analysis. Several methods are used to determine RNA quality. A commonly used technique is reverse transcriptase PCR amplification of housekeeping genes such as β-actin or GAPDH. RNA integrity is also tested by visualizing 28S and 18S rRNA after agarose gel electrophoresis. This method is now automated using a microcapillary electrophoresis system to provide an RNA integrity number (RIN) [8]. There is a spectrum of RIN numbers from the lowest integrity (1=total degradation) to the highest integrity (10=intact) [8]. This technique was compared to the traditional RT–PCR-based RNA integrity test, and there was good correlation between these two techniques [8,9].
Several studies have been performed to establish optimal conditions for RNA extraction from human ocular tissues. Wang and colleagues tested several different RNA preservation methods for human donor ocular tissues to extract high-quality RNA [10]. They found that death to preservation (DP) time, preservation in RNAlater, and the RNA extraction technique all affected overall RNA quality. Malik and colleagues examined the effects of DP time on RNA quality in the retina and retinal pigment epithelium of pig eyes [11]. Immediate postmortem enucleation as well as rapid dissection and freezing provided the best mRNA quality.
Although many of the eye tissues are vascularized, the eye also contains avascular tissues (i.e., the cornea, lens, trabecular meshwork, and sclera). DP time may differentially affect RNA quality in vascularized versus non-vascularized tissues. In the current study, we examined RNA quality in ten different vascularized and avascular human ocular tissues at various postmortem times using RIN analysis.
Donor eyes were provided by the Lion’s Eye Institute for Transplant and Research (LEITR; Tampa, FL). As shown in Table 1, 16 eyes from eight donors were collected at different DP times before preservation in RNAlater (Ambion Inc., Austin, TX) as described earlier [10]. Paired eyes were received and processed at LEITR within 2–6 h of death. A 2̴̴̴ 3 cm incision was made through the sclera and retina at the equator of each eye. One eye was immediately placed in 30 ml of RNAlater and stored at 4 °C. The contralateral eye was placed in a moist chamber at 4 °C for 8–48 h before being placed in 30 ml of RNAlater. The paired eyes were then shipped on ice to UNTHSC for dissection.
The following ocular tissues were carefully dissected from each donor eye: iris (I), sclera (S), trabecular meshwork (TM), cornea (C), retina (R), optic nerve head (ONH), optic nerve (ON), lens (L), choroid/retinal pigment epithelium (C/R), and ciliary body (CB). The majority of the eyes were pseudophakic, and the crystalline lens was present in only four donor eyes. In some eyes, clean tissue dissection was difficult, especially in eyes that had not been placed in RNAlater until >12 h DP time. Each dissected tissue was then placed in a 1.5 ml tube filled with RNAlater and stored in −80 °C until RNA extraction was performed.
Each eye tissue was homogenized in 1 ml of Iso-RNA Lysis Reagent (5 PRIME, Gaithersburg, MD) using a TissueLyser II (Qiagen, Germantown, MD). Total RNA was further extracted using RNeasy Micro Kits (Qiagen) as described in the manufacturer’s guide. Briefly, 50 μl of 4-Bromoanisole (BAN; Molecular Research Center, Cincinnati, OH) was added to tissue homogenates and mixed gently. After centrifugation at 12,000 ×g for 15 min at 4 °C, the aqueous phase was separated and mixed with the same volume of 100% ethanol. The aqueous phase and ethanol mixture was passed through an affinity column for RNA and washed. The column was washed again after DNase treatment and dried to remove the remaining ethanol. Total RNA was eluted in DNase/RNase free water.
The RNA integrity number (RIN) was determined in ten ocular tissues from 16 donor eyes using an Agilent 2100 Bioanalyzer (Agilent Technologies, Santa Clara, CA) with RNA nano- or picochip kit systems depending on the RNA concentration of each ocular tissue (Table 1). First, RNA nano- or picochips were primed using the chip priming station as described in the manufacturer’s instructions. The marker solution was loaded into each well of the RNA nano- or picochips followed by the loading of size markers and RNA samples. The chips were placed in an Agilent 2100 Bioanalyzer, and the RINs were determined using 2100 Expert Software (Agilent Technologies).
Statistical analysis was performed using GraphPad Prism Version 5.0 (GraphPad Software, San Diego, CA). For determining the time-dependent changes in the RIN, linear regression was performed to determine the R2 value and the significance between the DP time and the RIN. Data were also subjected to the paired Student t test or one-way analysis of variance (ANOVA) followed by a post hoc test (Bonferroni) for differences in the RINs between tissues. All data are expressed as means ± standard error of the mean (SEM). A p value of 0.05 or less was considered statistically significant.
RIN values were determined in ten ocular tissues from 16 donor eyes with various DP times (Table 1). RNA quality varied between ocular tissues processed at <6 h of DP time. The average RIN values varied from 4 to 7 among the ocular tissues placed in RNAlater within 6 h. of DP. RNA isolated from the cornea and the TM had significantly higher RIN values than RNA isolated from the ciliary body (Figure 1A; p<0.05). The overall RNA quality was significantly higher in non-vascular (NV) tissues (i.e., the cornea, lens, TM, and sclera) compared to the remaining vascularized (V) tissues (Figure 1B; p=0.0002). However, when RNA was extracted from tissues with DP times >8 h, the RIN values for all tissues were <6, and there were no statistically significant differences in RIN values between tissues (Figure 1C).
Shorter DP times enhanced RIN values in RNA isolated from the cornea (p<0.05), TM (p=0.0607), and ON, but had only modest to no effects on RNA quality from the iris and choroid/RPE (Figure 2). Representative RIN histograms for corneal RNA are shown based on different postmortem times (Figure 3A). In regression analysis, the RIN from corneal RNA was significantly (p<0.05) correlated with the DP time (Figure 3B; R2=0.26903). In contrast, the other ocular tissues did not show significant correlations between the RIN and the DP time.
We examined the effect of postmortem time on the quality of RNA isolated from human ocular tissues subsequent to RNAlater preservation. Ocular tissue RNA quality was determined as RIN values using a commercial bioanalyzer. We found that RNA quality deteriorated rapidly and was associated with DP time. There was a statistically significant correlation in RIN values with DP times in corneal tissues, but surprisingly not in the other ocular tissues. RNA quality was significantly higher at shorter DP times for the non-vascularized ocular tissues compared to the vascularized ocular tissues.
The quality of the postmortem human DNA was previously determined from the retina and iris. Wang et al. showed that total DNA from the postmortem human retina was significantly superior in quality and quantity compared to that from the postmortem human iris [12]. More relevantly, Malik and colleagues also simulated human donor eye postmortem times using porcine ocular tissues [11]. They studied RNA stability from RPE cells and retina tissues through RT–PCR analysis of housekeeping mRNAs and microchip analysis of 28S and 18S rRNA at various postmortem times. In the retina, expression of the abundant photoreceptor gene Rho was detected at all postmortem time ranges out to 48 h. However, in isolated RPE cells, the RPE-specific RPE65 mRNA showed relatively rapid decay after death. Their results demonstrated that RNA degradation varied by tissue and by the specific RNA analyzed. We also examined the effects of postmortem time on RNA integrity using ten different ocular tissues. One of the paired eyes was placed in RNAlater within 2–6 h, while the contralateral eye was placed in a moist chamber at 4 °C, simulating normal storage conditions for enucleated human eyes. These eyes were then placed in RNAlater 8–48 h postmortem (Table 1). We were somewhat surprised to find a good correlation between RNA quality and postmortem time for the corneal tissues only (Figures 3A,B). However, there was a significant correlation between the RNA quality and tissue vascularization with time to preservation <6 h (Figure 1B and Figure 2). RNA from avascular tissues had significantly higher RIN values compared to RNA isolated from vascularized tissues (Figure 1B). We speculate that the metabolic demands of vascularized tissues are more sensitive to the loss of nutrients postmortem, which leads to greater tissue and RNA degradation. It is also possible that the intrinsic RNase activity is higher in vascularized tissues. However, RNA quality was equally compromised in the majority of ocular tissues after 8 h postmortem (Figure 1C).
In this study, we determined the RNA integrity of ten human ocular tissues isolated from human donor eyes preserved at various postmortem times. From our data, we conclude that donor eyes should be preserved in RNAlater as soon as possible after enucleation to prevent potential loss of RNA quality. Importantly, an incision should be made through the sclera into the vitreous to facilitate penetration of this reagent into the eyes, and eyes should be kept at 4 °C until dissected, preferably no longer than 1 month. RNA quality diminished quickly, particularly in highly vascularized ocular tissues. Our findings provide guidance for analyzing gene expression from human donor ocular tissues.
This work was partially supported by a grant from the Lions Eye Institute for Transplant and Research (LEITR; Tampa, FL). The LEITR funded this research, and Abbot F. Clark is a member of the LEITR scientific advisory board. The authors have no other conflicts of interest.