Key words:
Amniotic membrane - cell attachment - gold sputter-coating - scaffold - scanning electron microscope
INTRODUCTION
Scanning electron microscope (SEM) is a widely used research tool that produces images of a sample by scanning it with a focused beam of electrons. SEM images provide precious information of a sample’s surface topography, composition, and properties. The correct sample preparation is essential to obtain clear images. SEM samples are required to be completely dry. Thus, biological samples of cells, tissues, and organisms require chemical fixation to preserve and stabilize their structure. This fixation is usually performed using a solution of aldehyde fixative agents such as glutaraldehyde, formaldehyde, and sometimes a combination of both or with other fixatives.[1]
[2] Most of the formaldehyde are existing as low polymers. The fixation process using formaldehyde takes longer time as the initial binding to protein is not completed before 24 h.[3] Glutaraldehyde has a larger molecule and a faster chemical fixative action due to the presence of more free aldehyde groups (−CHO).[2]
[4] Additional postfixation is optional and usually performed using osmium tetroxide.[5] Dehydration of the fixed tissues is then required. Air-drying is not recommended for dehydration as it may cause shrinkage and collapse to the fixed tissues. Alternatively, organic solvents such as acetone or ethanol are recommended for samples’ dehydration. These solvents replace water in the cells and tissues and thus preserve their structure. Hexamethyldisilazane (HMDS) is finally used for supercritical drying to remove liquid in a precise and controlled way. For electrically nonconductive specimens, sputter coated with gold, gold/palladium alloy, platinum, or other conductive materials is recommended to avoid image artifacts in the SEM images.[6] Alternatively, the samples can be impregnated in osmium to increase the bulk conductivity.[7]
Because of its special structure and composition, the amniotic membrane (AM) was nominated as a natural scaffold for tissue regeneration and engineering researches.[8]
[9]
[10] For SEM investigation of AM, most studies have used glutaraldehyde (2.5% or 4%) as a fixative agent, followed by postfixation in osmium tetroxide. Sputter coated with gold was almost always achieved before scanning.[11]
[12]
[13]
[14] This study aimed to compare glutaraldehyde-based protocol to formaldehyde-based protocol for the preparation of SEM sample to investigate stem cells cultured on human AM (hAM) scaffold.
MATERIALS AND METHODS
hAM of size 5 cm × 5 cm was obtained from Tissue Bank Unit, Universiti Sains Malaysia. Chemical de-epithelialization of hAM was achieved.[15] hAM was cut into 1 cm x 1 cm and immersed in thermolysin 125 μg/ ml (Sigma-Aldrich, USA) up to 25 min at room temperature. De-epithelialization was evaluated by a light microscope, and brushing technique by a cell scraper (TPP, Europe/Switzerland) was applied when necessary to remove the epithelial cells that could not be washed away by phosphate-buffered saline (PBS). Deciduous teeth stem cells (AllCells, USA) were seeded on the de-epithelialized hAM. All samples were incubated in a humidified atmosphere containing 95% air and 5% CO2 at 37°C incubator.
After 1–3 days, the samples were washed gently with PBS and fixed either using glutaraldehyde[16] or formaldehyde.[17] In brief, for the formaldehyde technique, the samples were immersed in 4% paraformaldehyde in 0.1 M phosphate buffer, pH 7.4 for 2 h at room temperature. Next, they were washed again with PBS and incubated with 8% formaldehyde at 4°C. After 2 days, the samples were washed in PBS and dehydrated in graded alcohol of 30%, 50%, 70%, 80%, 90%, and 100% (twice), each time for 10 min. For the glutaraldehyde technique, the samples were fixed in 2.5% glutaraldehyde for 2 h at 4°C. Then, the samples were washed in PBS and dehydrated again in a graded alcohol series. Finally, all the samples were incubated in HMDS for 10 min, air-dried in a desiccator, and mounted on suitable size plastic microscope slides [Figure 1]. Some samples were randomly selected to be coated with gold using a sputter coating machine. The samples were then scanned by an SEM (Phenom-World BV, Eindhoven, the Netherlands).
Figure 1: Mounting a human amniotic membrane sample on a plastic slide for scanning electron microscope
DISCUSSION
SEM is a useful tool in tissue engineering studies that provides good details of the morphological changes of cells and cell/scaffold interactions. However, following a suitable protocol for samples, preparation is required to produce images with a good quality. This pilot study was run to analyze and optimize different factors that might affect the quality of SEM images of hAM. The widely used technique to prepare AM for SEM in literature includes the use of glutaraldehyde (2.5%, 3%, or 4%) as a fixative agent.[11]
[18]
[19]
[20] In these studies, gold sputter coating of samples was traditionally performed after dehydration and drying.
Based on our findings in this study, formaldehyde results in better-quality SEM images when compared to glutaraldehyde as a fixative agent [Figure 2]. The aldehyde group (−CHO) is responsible for the fixative function of the aldehydes as it combines to protein and forms a cross-link–CH2, called a methylene bridge.[2] The glutaraldehyde molecule has two aldehyde groups. In aqueous solutions, glutaraldehyde is found as large polymers with the presence of free aldehyde groups (−CHO) of the polymer molecule on the side and the end of each unit.[4] These −CHO groups can largely contribute in the cross-linking as they combine with any protein they come in contact with. This explains why the chemical reaction of glutaraldehyde with protein is relatively fast (hours) and thus the advantage of rapid fixation of the tissues.[2] Whereas, the formaldehyde has a smaller molecule that dissolves rapidly in water to form methylene hydrate which exists as low polymers in aqueous solutions. Thus, glutaraldehyde has much greater potential for cross-linking when compared to formaldehyde. However, since it is present as larger molecules, its ability to penetrate tissue and biological molecules is less than formaldehyde. Hence, the unclear topography found in our study with glutaraldehyde samples may be interpreted by less penetration of the fixative through the hAM molecule within the used time. To avoid this problem, it is recommended to use glutaraldehyde solution which contains low polymers. This can be achieved using purified glutaraldehyde such as “EM grade” glutaraldehyde (Sigma-Aldrich, USA).[2] The preevaluation of the polymer size of glutaraldehyde available in our laboratory was not considered in this study.
Torn membrane or ruptured layer of cells was observed in some samples, regardless of the fixative agent used [Figure 3]. This indicates that ruptures in the sample surfaces were not caused by fixative material and were not related to fixation technique. This observation was interpreted as a sever shrinkage of the surface occurred during sample preparation and probably resulted from improper dehydration technique. Thus, a modification of the concentrations of diluted alcohol for the serial dehydration was suggested and tested. The new concentrations of graded alcohol chosen were 20%, 30%, 40%, 50%, 60%, 70%, 80% and 90%, one time for each and twice in 100% for 10 min each. Samples prepared following the new protocol with modified alcohol concentrations showed no torn features [Figure 5].
Figure 5: Scanning electron microscope images with different magnification for human amniotic membrane samples prepared with a new protocol adjusted based on the result of the pilot study. White spots and torn layers of cells or membranes were not observed
In some specimens, small, randomly diffused white spots were observed [Figure 4]. These spots were regarded as contamination which occurred during the preparation process probably due to salt crystals of the used buffer. Thus, to eliminate the production of the white spots, it was decided to filter the 4% paraformaldehyde in 0.1 M phosphate buffer, pH 7.4 solution using 0.20 μm sterile filter unit before used. Samples prepared using filtered paraformaldehyde showed no white spots in the SEM image [Figure 5].
Gold sputter coating of hAM specimen was not found to improve the quality of SEM images [Figure 6a]
[b]. On contrast, interactions of cells on membrane were shown better in non-sputter-coated specimens. Coating the surface of nonconductive specimen with conductive material is usually indicated to prevent the accumulation of electrostatic charge that may cause scanning faults. Gold sputter coating of AM was routinely achieved in previous SEM studies.[11]
[12]
[13]
[14] However, since hAM is a biological specimen, it should be considered as a conductive material. The results of this study suggested that the conductive property of the hAM is sufficient to provide good-quality SEM images and no extra coating is needed. This will save time and cost for SEM preparation.
Figure 6: Effects of sputter gold coating on stem cells seeded on human amniotic membrane for scanning electron microscope analysis. Gold sputter-coated specimen (a) did not improve the image of the one without (b). The image of b Showed better interactions of cells on membrane (×5000)
CONCLUSIONS
To obtain clear SEM images of AM samples, it is recommended to run a preliminary study to determine the better chemicals and conditions to prepare the samples even if following preexisting protocols. Formaldehyde protocol described in this study is suitable to prepare hAM samples for SEM study. However, it is recommended to filter the paraformaldehyde buffer using 0.20 μm sterile filter unit and modify the concentrations of graded alcohol to be 20%, 30%, 40%, 50%, 60%, 70%, 80%, and 90%, one time for each and twice in 100% for 10 min each. Gold sputter coating of samples is not indicated for hAM specimen prepared for SEM study.
Financial support and sponsorship
Nil.
