Nanomechanical characterization of the stiffness of eye lens cells: a pilot study.

PURPOSE: The purpose of this study is to probe the mechanical properties of individual eye lens cells isolated from nucleus and cortex of adult sheep eye lens, and to characterize the effect of cytoskeletal drugs. METHODS: We used atomic force microscopy (AFM), featuring a spherical tip at the end of a soft cantilever, to indent single lens cells, and measure the Young's modulus of isolated nuclear and cortical lens cells. Measurements were performed under basal conditions, and after addition of drugs that disrupt actin filaments and microtubules. RESULTS: We found that single lens cells were able to maintain their shape and mechanical properties after being isolated from the lens tissue. The median Young's modulus value for nuclear lens cells (4.83 kPa) was ~ 20-fold higher than for cortical lens cells (0.22 kPa). Surprisingly, disruption of actin filaments and microtubules did not affect the measured Young's moduli. CONCLUSIONS: We found that single cells from the lens nucleus and cortex can be distinguished unambiguously using the elastic modulus as a criterion. The uncommon maintenance of shape and elastic properties after cell isolation together with the null effect of actin filaments and microtubules targeting drugs suggest that the mechanical stability of fiber cells is provided by cellular elements other than the usual cytoskeletal proteins.

Age-related compaction of lens fibers affects the structure and optical properties of rabbit lenses.

BACKGROUND: The goal of this investigation was to correlate particular age-related structural changes (compaction) to the amount of scatter in rabbit lenses and to determine if significant fiber compaction occurred in the nuclear and inner cortical regions. METHODS: New Zealand White rabbits at 16-20 months old (adult; n = 10) and at 3.5-4 years old (aged; n = 10) were utilized for this study. Immediately after euthanising, scatter was assessed in fresh lenses by low power helium-neon laser scan analysis. Scatter data was analyzed both for whole lenses and regionally, to facilitate correlation with morphometric data. After functional analysis, lenses were fixed and processed for scanning electron microcopy (SEM; right eyes) and light microscopy (LM; left eyes). Morphometric analysis of SEM images was utilized to evaluate compaction of nuclear fibers. Similarly, measurements from LM images were used to assess compaction of inner cortical fibers. RESULTS: Scatter was significantly greater in aged lenses as compared to adult lenses in all regions analyzed, however the difference in the mean was slightly more pronounced in the inner cortical region. The anterior and posterior elliptical angles at 1 mm (inner fetal nucleus) were significantly decreased in aged vs. adult lenses (anterior, p = 0.040; posterior, p = 0.036). However, the average elliptical angles at 2.5 mm (outer fetal nucleus) were not significantly different in adult and aged lenses since all lenses examined had comparable angles to inner fetal fibers of aged lenses, i.e. they were all compacted. In cortical fibers, measures of average cross-sectional fiber area were significantly different at diameters of both 6 and 7 mm as a function of age (p = 0.011 and p = 0.005, respectively). Accordingly, the estimated fiber volume was significantly decreased in aged as compared to adult lenses at both 6 mm diameter (p = 0.016) and 7 mm diameter (p = 0.010). CONCLUSION: Morphometric data indicates that inner cortical fibers undergo a greater degree of age-related compaction than nuclear fibers. Increased scatter appears to be only tentatively correlated with regions of fiber compaction, suggesting that it is simply one of an array of factors that contribute to the overall decreased transparency in aged rabbit lenses.

Modeling internal stress distributions in the human lens: can opponent theories coexist?

The effects of material properties and equatorial stretching forces on the stress distribution and shape profile of human lenses were investigated to see whether support could be found for either or both current theories of accommodation. Finite element analysis was used to create models using shape parameters and material properties from published data. Models were constructed for two lenses of different ages. Material properties were varied to show differences between models with a single elastic modulus and those with different moduli for the cortex and the nucleus. Two levels of stretching forces were applied at the equator. Comparisons between experimental and model profiles were made, and stress distribution patterns were constructed. In all models, stretching produces a flattening in the peripheral curvature of the lens. In the younger lens, model and experimental results show that central curvature at some points is steeper for stretched than for unstretched profiles. In the older lens, gradients are flatter at all central points for stretched model and experimental profiles compared to the unstretched profile. In all models, there is a region of higher stress distribution within the lens that corresponds with the position of an inflection point that appears on the anterior surface and, in the older lens, also on the posterior surface. The results show that equatorial stretching forces can produce shape changes in support of both current theories of accommodation depending on the lens age, shape, and applied force.

Insights into the age-related decline in the amplitude of accommodation of the human lens using a non-linear finite-element model.

AIM: To understand the effect of the geometric and material properties of the lens on the age-related decline in accommodative amplitude. METHODS: Using a non-linear finite-element model, a parametric assessment was carried out to determine the effect of stiffness of the cortex, nucleus, capsule and zonules, and that of thickness of the capsule and lens, on the change in central optical power (COP) associated with zonular traction. Convergence was required for all solutions. RESULTS: Increasing either capsular stiffness or capsular thickness was associated with an increase in the change in COP for any specific amount of zonular traction. Weakening the attachment between the capsule and its underlying cortex increased the magnitude of the change in COP. When the hardness of the total lens stroma, cortex or nucleus was increased, there was a reduction in the amount of change in COP associated with a fixed amount of zonular traction. CONCLUSIONS: Increasing lens hardness reduces accommodative amplitude; however, as hardness of the lens does not occur until after the fourth decade of life, the age-related decline in accommodative amplitude must be due to another mechanism. One explanation is a progressive decline in the magnitude of the maximum force exerted by the zonules with ageing.

Can reliable values of Young's modulus be deduced from Fisher's (1971) spinning lens measurements?

The current textbook view of the causes of presbyopia rests very largely on a series of experiments reported by R.F. Fisher some three decades ago, and in particular on the values of lens Young's modulus inferred from the deformation caused by spinning excised lenses about their optical axis (Fisher 1971) We studied the extent to which inferred values of Young's modulus are influenced by assumptions inherent in the mathematical procedures used by Fisher to interpret the test and we investigated several alternative interpretation methods. The results suggest that modelling assumptions inherent in Fisher's original method may have led to systematic errors in the determination of the Young's modulus of the cortex and nucleus. Fisher's conclusion that the cortex is stiffer than the nucleus, particularly in middle age, may be an artefact associated with these systematic errors. Moreover, none of the models we explored are able to account for Fisher's claim that the removal of the capsule has only a modest effect on the deformations induced in the spinning lens.

Age dependence of dielectric properties of bovine brain and ocular tissues in the frequency range of 400 MHz to 18 GHz.

In order to identify possible age-dependent dielectric properties of brain and eye tissues in the frequency range of 400 MHz to 18 GHz, measurements on bovine grey and white matter as well as on cornea, lens (cortical) and the vitreous body were performed using a commercially available open-ended coaxial probe and a computer-controlled vector network analyser. Freshly excised tissues of 52 animals of two age groups (42 adult animals, i.e. 16-24 month old and 10 young animals, i.e. 4-6 month old calves) were examined within 8 min (brain tissue) and 15 min (eye tissue), respectively, of the animals' death. Tissue temperatures for the measurements were 32+/-1 degrees C and 25+/-1 degrees C for brain and eye tissues, respectively. Statistical analysis of the measured data revealed significant differences in the dielectric properties of white matter and cortical lens tissue between the adult and the young group. In the case of white matter the mean values of conductivity and permittivity of young tissue were 15%-22% and 12%-15%, respectively, higher compared to the adult tissue in the considered frequency range. Similarly, young cortical lens tissue was 25%-76% higher in conductivity and 27%-39% higher in permittivity than adult cortical lens tissue.

Changes in the internal structure of the human crystalline lens with age and accommodation.

Scheimpflug images were made of the unaccommodated and accommodated right eye of 102 subjects ranging in age between 16 and 65 years. In contrast with earlier Scheimpflug studies, the images were corrected for distortion due to the geometry of the Scheimpflug camera and the refraction of the cornea and the lens itself. The different nuclear and cortical layers of the human crystalline lens were determined using densitometry and it was investigated how the thickness of these layers change with age and accommodation. The results show that, with age, the increase in thickness of the cortex is approximately 7 times greater than that of the nucleus. The increase in thickness of the anterior cortex was found to be 1.5 times greater than that of the posterior cortex. It was also found that specific parts of the cortex, known as C1 and C3, showed no significant change in thickness with age, and that the thickening of the cortex is entirely due to the increase in thickness of the C2 zone. With age, the distance between the sulcus (centre of the nucleus) and the cornea does not change. With accommodation, the nucleus becomes thicker, but the thickness of the cortex remains constant.

Changes in the refractive index of lens fibre membranes during maturation--impact on lens transparency.

PURPOSE: Local variations in refractive index are the physical cause of light scattering in a material or tissue and also induce phase changes of propagating light waves. The goal of this study was to analyse local differences in refractive index by phase contrast microscopy of sections of human lenses. METHODS: Refractive index was estimated by immersion refractometry. Cryo-sections of quick-frozen human donor lenses were embedded in a graded series of bovine serum albumin solutions, and in immersion oil, ranging in refractive index from 1.34 to 1.52. RESULTS: Fibre membranes in the lens cortex prove to have a refractive index considerably above that of fibre cytoplasm at the same location. Fibre membranes in the lens nucleus have a refractive index approximately the same as that of fibre cytoplasm at the same location. CONCLUSION: In the lens cortex, transparency is obtained by a high spatial order of the lens fibre lattice to compensate for the light scattering caused by differences in refractive index between fibre membranes and cytoplasm. In the lens nucleus, high spatial order is less important, because the minor differences in the refractive index between fibre membranes and fibre cytoplasm lead only to minimal scattering.

Relaxographic studies of aging normal human lenses.

Ten excised normal human lenses of various ages were studied. Seven sections of each lens, from anterior outer cortex to posterior outer cortex were imaged and the T(1) (spin-lattice) and T(2) (spin-spin) relaxation data on each section were collected. T(1) and T(2) relaxation were analysed by fitting pixel intensity to one term exponential expressions. Both T(1) and T(2) relaxation times showed minimal values in the nuclear region and maxima at the two outer cortexes. The pre-exponential terms of the fittings of both T(1) and T(2) relaxation,M(1) and M(2), were normalized in order to eliminate instrumental variations over a 2 year period. M(2) had a maximum in the nucleus and minima in the two cortexes. M(1) exhibited minimal value in the nucleus and maxima at the two cortexes. The positional dependence of T(2) relaxation times as well as that of M(2) indicated that they represent the behavior of the bound water in the lens. The positional dependence of M(1) suggests that this relaxation represents the total water that has a minimal value in the nucleus. The T(2) relaxation time decreases with increase in the age of the lens at each location. The slope of the change in T(2) relaxation time with age is greatest in the outer cortexes and diminishes as one proceeds to the nucleus. T(1) relaxation times and M(1) do not show significant change with age. This and the age dependence of the other relaxographic parameters imply that the aging of the lens involves major changes in its hydration properties that are more accentuated in the cortexes. The interpretation of these changes is in agreement with the syneretic theory of lens aging.

Estimation of anterior nucleus of lens by Scheimpflug image before and after pupil dilatation.

PURPOSE: To compare the accuracy of lens transparency evaluations by Scheimpflug image in the anterior nucleus of the lens before and after pupil dilatation. METHODS: Scheimpflug lens images were recorded in 70 eyes of 38 subjects (age: 28-75 years) before and after pupil dilatation, and light scattering intensity measurements before and after dilatation were compared. RESULTS: There was a significant positive correlation between the light scattering intensity before and after dilatation at the anterior cortex, anterior nucleus, and central clear zone of the lens (r > 0.9, P <.0001). CONCLUSIONS: It is possible to estimate the transparency in the anterior nucleus of the lens from the Scheimpflug image without pupil dilatation. If nuclear type cataracts are regarded as a structural marker of aging in epidemiological studies, measuring the light scattering intensity in the anterior nucleus of the lens without dilatation seems to be a safe, useful, and quantitative method.

The role of MIP in lens fiber cell membrane transport.

MIP has been hypothesized to be a gap junction protein, a membrane ion channel, a membrane water channel and a facilitator of glycerol transport and metabolism. These possible roles have been indirectly suggested by the localization of MIP in lens gap junctional plaques and the properties of MIP when reconstituted into artificial membranes or exogenously expressed in oocytes. We have examined lens fiber cells to see if these functions are present and whether they are affected by a mutation of MIP found in CatFr mouse lens. Of these five hypothesized functions, only one, the role of water channel, appears to be true of fiber cells in situ. Based on the rate of volume change of vesicles placed in a hypertonic solution, fiber cell membrane lipids have a low water permeability (pH2O) on the order of 1 micron/sec whereas normal fiber cell membrane pH2O was 17 micron/sec frog, 32 micron/sec rabbit and 43 micron/sec mouse. CatFr mouse lens fiber cell pH2O was reduced by 13 micron/sec for heterozygous and 30 micron/sec for homozygous mutants when compared to wild type. Lastly, when expressed in oocytes, the pH2O conferred by MIP is not sensitive to Hg2+ whereas that of CHIP28 (AQP1) is blocked by Hg2+. The fiber cell membrane pH2O was also not sensitive to Hg2+ whereas lens epithelial cell pH2O (136 micron/sec in rabbit) was blocked by Hg2+. With regard to the other hypothesized roles, fiber cell membrane or lipid vesicles had a glycerol permeability on the order of 1 nm/sec, an order of magnitude less than that conferred by MIP when expressed in oocytes. Impedance studies were employed to determine gap junctional coupling and fiber cell membrane conductance in wild-type and heterozygous CatFr mouse lenses. There was no detectable difference in either coupling or conductance between the wild-type and the mutant lenses.

Conservation of gene expression during embryonic lens formation and cornea-lens transdifferentiation in Xenopus laevis.

Few molecular comparisons have been made between the processes of embryogenesis and regeneration or transdifferentiation that lead to the formation of the same structures. In the amphibian, Xenopus laevis, the cornea can undergo transdifferentiation to form a lens when the original lens is removed during tadpole larval stages. Unlike the process of embryonic lens induction, cornea-lens transdifferentiation is elicited via a single inductive interaction involving factors produced by the neural retina. In this study, we compared the expression of a number of genes known to be activated during various phases of embryonic lens formation, during the process of cornea-lens transdifferentiation. mRNA expression was monitored via in situ hybridization using digoxigenin-labeled riboprobes of pax-6, Xotx2, xSOX3, XProx1, and gamma6-cry. We found that all of the genes studied are expressed during both embryogenesis and cornea-lens transdifferentiation, though in some cases their relative temporal sequences are not maintained. The reiterated expression of these genes suggests that a large suite of genes activated during embryonic lens formation are also involved in cornea-lens transdifferentiation. Ultimately functional tests will be required to determine whether they actually play similar roles in these processes. It is significant that the single inductive event responsible for initiating cornea-lens transdifferentiation triggers the expression of genes activated during both the early and late phases of embryonic lens induction. These findings have significant implications in terms of our current understanding of the "multistep" process of lens induction. Dev Dyn 1999;215:308-318.

Quantitative determination of gap junctional permeability in the lens cortex.

We have developed a simple dye transfer method, which allows the gap junction permeability of lens fiber cells to be quantified. Two fixable fluorescent dyes (Lucifer yellow and rhodamine-dextran) were introduced into peripheral lens fiber cells via mechanical damage induced by removing the lens capsule. After a defined incubation period, lenses were fixed, sectioned, and the distribution of the dye recorded using confocal microscopy. Rhodamine-dextran and Lucifer yellow both labeled the extracellular space between fiber cells and the cytoplasm of fiber cells that had been damaged by capsule removal. For the gap junctional permeable dye Lucifer yellow, however, labeling was not confined to the damaged cells and exhibited intercellular diffusion away from the damaged cells. The extent of dye diffusion was quantified by collecting radial dye intensity profiles from the confocal images. Effective diffusion coefficients (D eff) for Lucifer yellow were then calculated by fitting the profiles to a series of model equations, which describe radial diffusion in a sphere. D eff is the combination of dye diffusion through the cytoplasm and through gap junction channels. To calculate the gap junctional permeability (Pj) an estimate of the cytoplasmic diffusion coefficient (Dcyt = 0.7 x 10(-6) cm2/sec) was obtained by observing the time course of dye diffusion in isolated elongated fiber cells loaded with Lucifer yellow via a patch pipette. Using this approach, we have obtained a value for Pj of 31 x 10(-5) cm/sec for fiber-fiber gap junctions. This value is significantly larger than the value of Pj of 4.4 x 10(-6) cm/sec reported by Rae and coworkers for epithelial-fiber junctions (Rae et al., 1996. J. Membrane Biol. 150:89-103), and most likely reflects the high abundance of gap junctions between lens fiber cells.

A distinct membrane current in rat lens fiber cells isolated under calcium-free conditions.

PURPOSE: To investigate whether lens fiber cells isolated and maintained under calcium-free conditions exhibit distinct membrane currents. METHODS: Fiber cells were isolated from the cortical portion of neonate rat lenses using a trypsin digestion protocol and were maintained in EDTA-buffered Ringer's solutions. Membrane currents were recorded from fiber bundles using the whole-cell patch-clamp technique. RESULTS: Cortical fiber cells of up to 600-microm length were viable and amenable to whole-cell patch-clamp recording. The major current recorded under these conditions was a slowly activating, voltage-dependent current that was markedly increased on membrane depolarization. This current appeared to be fiber cell specific and had similar properties to currents elicited by gap junction hemichannels previously recorded by others in Xenopus oocytes. CONCLUSIONS: This is the first report of whole-cell patch-clamp recordings from intact elongated fiber cells. Fiber cells kept in calcium-free bath medium appear to be electrically "leaky" and exhibit a distinct membrane current that has not been described previously for lens cells. This current is unlikely to be active in the normal lens but may play a role in the depolarized cataractogenic lens.

Electrical impedance tomography of the eye: in vitro measurements of the cornea and the lens.

This study was designed to perform multifrequency impedance measurements on the pig's eye. On one hand, impedance of the ocular tissues was measured from 10 kHz to 10 MHz. The aqueous and vitreous humours and the cornea showed no relaxation in this range of frequencies, whereas the lens and its parts (the cortex and the nucleus) did. On the other hand, multifrequency EIT and dynamic imaging were performed on the lens and on the whole eye. Data and images obtained after thermal and chemical injuries are presented and discussed.

Expression of transforming growth factor beta in the embryonic avian lens coincides with the presence of mitochondria.

During their maturation, lens cells lose all membrane bound organelles, including mitochondria. In chicken embryos this process begins in the central lens fibers beginning around embryonic day 12 (E12). Transforming growth factor beta (TGF beta) is a multipotent growth modulator thought to play a role in numerous developmental processes. TGF beta 1 has been localized to mitochondria in rat liver cells and muscle cells. In the present study, we examined the expression of TGF beta isoform mRNAs and proteins during chicken embryonic lens development. PCR analysis demonstrated TGF beta 2 and TGF beta 3 transcripts in the lens epithelium and fibers throughout pre- and post-hatching development. TGF beta isoforms were detected throughout the lens epithelium and fibers early in development (E6). However by E19, the distribution of TGF beta 2 and TGF beta 3 transcripts and proteins coincided with regions of the lens that contained mitochondria. In addition, intense TGF beta staining was observed in the basal portions of the equatorial epithelial cells, a region with abundant mitochondria. Transcripts for TGF beta 1 and TGF beta 4 were not detected in any tissue or time frame examined. Similarly, no immunostaining for TGF beta 1 was observed.

[A real-time analysis of 133 normal lens images by a computer].

According to the theory that the light scattering of the lens is correlated with the lens density, we designed a computerized system for the real-time analysis of the lens image. By measurement of the gray scale value of the lens optical section, the lens density is measured objectively and numerically. With the help of the system, 133 normal lens images were investigated. From the analysis of various age groups, we found that the grey scale values of the anterior cortex, posterior cortex and nucleus increase with the increase of age (P < 0.01), the grey scale values of the anterior and posterior cortex are significantly higher than the value of the nucleus (P < 0.05), but there is no significant difference between the values of the anterior and posterior cortex (P > 0.05), and there is also no significant difference in the comparisons of the grey scale values of the respective corresponding lens areas between the male and female.

Different regional changes of fluorescence spectra of clear human lenses and nuclear cataracts.

Fluorescence spectra are recorded from the cortex and nucleus of the same human lenses [clear and cataracta brunescens (nigra) with colorless cortex]. When comparing clear cortices with either the harder nucleus of a clear lens, or a cataracta brunescens for a given excitation wavelength, a shift of the fluorescence maxima of the nucleus to longer wavelengths is observed. The shift appears to be independent of the degree of coloring since it is very similar for different nuclei, and it is not increased in cataracta nigra. The fluorescence intensities are similar when comparing the clear cortex of clear lenses and cataracta brunescens. For the nuclei, however, the intensity increases by up to four to six times with increasing coloring. For constant excitation wavelength, the fluorescence band maximum of the nucleus (of clear lenses and of cataracta brunescens) exhibits roughly the same shift to longer wavelengths as that of the cortex. Upon 320 nm excitation the fluorescence intensity of a cataracta nigra is about twice that of a clear lens of juvenile age. Upon 380 nm excitation the factor increases to four. Therefore in older and colored lens nuclei a red shift of the fluorescence maximum with increasing excitation wavelength is observed. We discuss whether or not the changes in the molecular proteins, in addition to advanced glycolization end products, may be responsible for the different fluorescence properties (and the brown color) with increasing age.

Colloid osmotic pressure of steer crystallins: implications for the origin of the refractive index gradient and transparency of the lens.

The osmotic behavior of soluble cortical and nuclear steer lens crystallins was characterized by secondary osmometry for several ionic strength and pH conditions. Osmotic pressure versus protein concentration relationships were measured for pressures up to 1.15 x 10(6) dyn cm-2. At low concentrations (< 0.2 g ml-1), the osmotic pressure increased linearly with pressure, whereas for concentrations above 0.2 g ml-1, the pressure rose more sharply, giving progressively larger changes in osmotic pressure with increasing crystallin concentration. At a given ionic strength and applied osmotic pressure, the nuclear proteins attained a higher protein concentration than did the cortical proteins. For example, at the highest osmotic pressure of 1.15 x 10(6) dyn cm-2 at pH 7.6 and 0.1 M ionic strength, the observed protein concentrations were 0.43 g ml-1 for the cortical proteins and 0.52 g ml-1 for the nuclear proteins. For both cortical and nuclear steer crystallins, the pressure rose more steeply with concentration than do pressures for calf crystallins described in the literature. The impact of these developmental differences in osmotic pressure on lens transparency is discussed. Both the nuclear and cortical crystallins exhibited ionic strength-dependent shifts in their pressure-concentration behavior. At 0.02 M ionic strength, higher pressures were observed, whereas at 0.4 M ionic strength lower pressures were observed for a given protein concentration. The crystallins were also found to equilibrate to different protein concentrations at a constant osmotic pressure and 0.1 M ionic strength over a pH range of 4-9, with a maximum concentration around pH 5 for the cortical crystallins and pH 6 for the nuclear crystallins. Thus, the adult bovine cortical and nuclear soluble lens extracts are different in their osmotic properties, reflecting underlying differences in protein composition. The results of the ionic strength and pH experiments suggest that hard-sphere, electrostatic, and Donnan forces contribute to the total colloid osmotic pressure of the lens crystallins. However, near physiologic pH and ionic strength the charges of the proteins are screened to the extent that the colloid osmotic pressure exhibits only minor changes for large changes in ionic conditions. The differences in the osmotic behavior of the cortical and nuclear proteins are consistent with a model where regional variations in the colloid osmotic properties of the proteins across the lens help support the radial refractive index gradient that is present in vertebrate lenses. The importance of a radial concentration gradient of metabolites is also discussed.

Changes in light scatter and width measurements from the human lens cortex with age.

Light scatter and width measurements of the anterior cortical layers of the human lens were made in 50 eyes of 50 subjects using computerised linear scanning densitometry of Scheimpflug images. It was demonstrated that the amount of light scatter increased with age in all of the three major zones and that zone C3 showed the most marked increase. Most lens growth occurs in zone C2 with C3 showing little increase in width once it has become established. Zone C1 showed a tendency to decrease in width with age. In addition it was shown that the C3 zone, which is not present at birth and during early childhood, appears as a distinct layer during the second decade of life. Its scattering properties continue to increase throughout life, exceeding all other zones after approximately 30 years of age, in the absence of cataract. Possible explanations for the lens zone pattern are discussed.