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A neuropathologic study of three cases of prosaposin (pSap) deficiency (ages at death 27, 89 and 119 days), carried out in the standard autopsy tissues, revealed a neurolysosomal pathology different from that in the non-neuronal cells. Non-neuronal storage is represented by massive lysosomal accumulation of glycosphingolipids (glucosyl-, galactosyl-, lactosyl-, globotriaosylceramides, sulphatide, and ceramide). The lysosomes in the central and peripheral neurons were distended by pleomorphic non-lipid aggregates lacking specific staining and autofluorescence. Lipid storage was borderline in case 1, and at a low level in the other cases. Neurolysosomal storage was associated with massive ubiquitination, which was absent in the non-neuronal cells and which did not display any immunohistochemical aggresomal properties. Confocal microscopy and cross-correlation function analyses revealed a positive correlation between the ubiquitin signal and the late endosomal/lysosomal markers. We suppose that the neuropathology most probably reflects excessive influx of non-lipid material (either in bulk or as individual molecules) into the neurolysosomes. The cortical neurons appeared to be uniquely vulnerable to pSap deficiency. Whereas in case 1 they populated the cortex, in cases 2 and 3 they had been replaced by dense populations of both phagocytic microglia and astrocytes. We suggest that this massive neuronal loss reflects a cortical neuronal survival crisis precipitated by the lack of pSap. The results of our study may extend the knowledge of the neurotrophic function of pSap, which should be considered essential for the survival and maintenance of human cortical neurons.
Prosaposin (pSap) deficiency is a rapidly progressive fatal neurovisceral lysosomal storage disorder caused by mutations in the PSAP gene which leads to the blockage of pSap protein translation or to the premature (intranuclear) nonsense-mediated decay of pSap mRNA [13, 25, 43, 54]. The proven genotypes result in the absence of pSap and the products of pSap proteolytic processing. These polypeptide products, called saposins (Saps, sphingolipidhydrolase activating proteins), are essential for activating a set of lysosomal sphingolipid hydrolases . In the absence of Saps, the sphingolipid substrates remain undegraded. The accumulated substrates, in visceral cell types, cause the lysosomes to become distended, giving them a foamy appearance and the process ultimately ends in organ failure, similar to full blown classic lipid storage disorders [3, 13, 25]. In this study, we show that in pSap deficiency the neurolysosomes of both the peripheral and central neurons express a distinct pathology, which may indicate a process resembling autophagocytosis. Given the opportunity to compare the cortical structure at the earliest stage of the disease to that in the more advanced stages, we were able to describe a unique failure of cortical neurons to survive after reaching the cerebral cortex. We would like to characterize this destructive phenomenon, precipitated by the absence of pSap, as a cortical neuronal survival crisis, which seems to be a feature of human pSap deficiency. This fits well with the concept of pSap having fundamental neurotrophic functions .
Formaldehyde fixed paraffin embedded (FFPE) tissue samples were available from three cases of verified pSap deficiency. The life spans of the cases were: 27 days (case 1 ), 89 days (case 2 ) and 119 days (case 3 ). In two of the three cases (27, 119 days) we were kindly provided by colleagues from the pathology departments unembedded routinely formaldehyde fixed samples of several cortical and subcortical brain areas. The tissue samples available were as follows: case 1 (27 days)–parts of the frontal and insular cortex, striatum, pallidum, thalamus, and adjacent parts of the white matter; case 2 (89 days)–several cortical samples, thalamus, and basal ganglia; and case 3 (119 days)–cerebral cortex from all lobes, cerebellum, pons, medulla oblongata and spinal cord.
The tissue sections (5 μm) were dewaxed, hydrated and hematoxylin-eosin stained. The primary antibodies and their respective dilutions used for immunohistochemistry are listed in Table 1. The primary antibodies (incubated overnight at 4°C) were detected with appropriate Envision TM kits (DAKO, Copenhagen, Denmark) or rabbit anti-guinea pig HRP labeled secondary antibody (DAKO).
In conjunction, various neurolysosomal storage disorders (previously defined biochemically at the Institute of Inherited Metabolic Disorders) were studied to follow neuronal ubiquitination (for the list, see Results). The FFPE tissue samples from various parts of the brain were examined together with the samples of storage affected visceral organs.
The sections of the formaldehyde fixed unembedded samples (cases 1 and 2) were processed for electron microscopy after osmification, using standard dehydration in ethanol and embedding in an Araldite–Epon mixture. The paraffin embedded samples of the pons (case 3) were processed for electron microscopy after deparaffination, hydration, and osmification.
The residual lipids extracted from the paraffin embedded brain samples were analyzed using a procedure recently described .
The FFPE paraffin embedded tissue sample from the spinal cord (case 3) was chosen for immunofluorescence multiple labeling colocalization analysis. The tissue sections were treated as described above. The primary antibodies and their dilutions used for immunofluorescence labeling are listed in Table 1.
The combinations of the primary antibodies were as follows: anti-LAMP2/anti-ubiquitin, anti-cathepsin D/anti-ubiquitin, anti-LAMP2/anti-60 kDa antigen of human mitochondria, anti-PDI/anti-ubiquitin, anti-60 kDa antigen of human mitochondria/anti-ubiquitin. The details of the tissue section processing and staining protocol for both immunohistochemistry and immunofluorescence labeling are available from the authors upon request.
Images (xy sampled at the maximum of z fluorescence intensity) were acquired using a Nikon Eclipse E800 microscope equipped with a C1 confocal head and 488, 543 and 633 nm laser lines and appropriate 515 ± 15 nm, 590 ± 15 nm and 650LP band pass filters. The sampling density was corrected to conform to the Nyquist criterion according to the objective lens used (Nikon Plan Apo 60 × 1.4 N.A.). The microscope settings including laser intensity, pinhole size, pixel dwell times; photomultiplier gains were kept constant for all image acquisitions and the images were checked for the presence of spectral cross-talk.
Point spread functions (PSF) at appropriate excitation/detection wavelengths were measured using PS-Speck Microscope Point Source Kit (Invitrogen- Molecular Probes, Carlsbad, CA).
The cerebral cortex sample from (case 2, day 89) was double-labeled with mouse monoclonal anti-CD 68 and rabbit polyclonal anti-GFAP antibodies. Secondary detections were performed using donkey anti-mouse IgG Alexa Fluor 555 and goat anti-rabbit IgG Alexa Fluor 488 antibodies (Invitrogen- Molecular Probes, Carlsbad, CA) diluted 1:500.
Between 25 and 30 images of neurons of the spinal cord anterior columns were acquired and further processed for each of the double-labeling experiments. The images were restored based on deconvolution using an appropriately measured PSF with a classical maximum likelihood estimate algorithm (Huygens Professional software, SVI, Hilversum, Netherlands). Only pixels included in the neurons were further evaluated without any additional thresholding or pixel intensity manipulation. Cross-correlation function analysis  was performed using a Tcl/Tk script employing the Huygens Scripting modality in Huygens Professional software. Single pixel shifts with parallel Pearson’s coefficient calculations were applied to the red channel of the images with respect to the green channel to the extent of −4 to +4 μm (only values −3 to +3 μm are shown, Fig. 5). The appropriate pixel shifted Pearson’s coefficient values were calculated for each individual evaluated shifted image. The median values and 5/95 percentile values and first and third quartile values of Pearson’s coefficient were plotted on the y axis for each single pixel shifted position (x axis) to get the final cross-correlation curves and to document the distribution of the values.
The Pearson’s coefficient values range from −1 to +1. Positive Pearson’s coefficient values at Δx = 0 demonstrate significant overlap (colocalization) of the signals, negative values demonstrate repulsion (anti-colocalization) of the signals, and values around zero demonstrate a random distribution of signals. The details of the Tcl/Tk script used to calculate CCF is available from the authors upon request. All the image manipulations and figure preparations were performed using Huygens Professional or ImageJ (NIH, http://www.rsb.info.nih.gov/ij/) software.
In order to avoid any ambiguity, the use of neurolysosomal in this paper refers to the lysosomal compartment of neurons.
The general neuropathologic findings in all the three cases have already been published [13, 14, 25]. However, to briefly summarize, the neuronal perikarya were variably distended by fine eosinophilic non-autofluorescent granules (Figs. 1a inset, inset,2a).2a). Neuronal storage was present in all the regions available for examination: brain cortex (see below), basal ganglia, thalamus, pons, medulla oblongata, spinal cord, and cerebellum. The only exception was the subventricular zone (cases 1 and 2) which was cellular and devoid of histological and immunohistochemical abnormalities. There was a marked difference between the brain cortical pathology in case 1 as compared to cases 2 and 3 (see below). Storage was manifested in the peripheral nervous system in all samples available (gut, lung, liver, kidney, and urinary bladder).
The following data represent novel and previously unreported features of the neurolysosomal storage process in pSap deficiency.
Contrary to the foamy appearance of the storage cells in the visceral region, the neuronal perikarya were distended even ballooned by a uniform population of fine eosinophilic granules. In case 3, their appearance changed to granulovacuolar (Fig. 2b). The granules were not autofluorescent and did not exhibit any distinct staining in routine histological stainings. Lipid histochemistry showed an absence of birefringence and no significant detectable amounts of glycolipids and sphingolipids .
In contrast to the neurons the astrocytes displayed significantly milder storage changes [13, 25]. Regarding the oligodendroglia, the lysosomal storage has never been demonstrated [13, 17]. Changes of microglial phagocytes are discussed below.
Electron microscopy (cases 1 and 2) showed vacuoles approximately 0.5 μm in diameter containing numerous dense granules of various densities, 45–230 nm in diameter, sometimes with amorphous or coarse membranous substructure, occasionally resembling degraded mitochondria (Fig. 3). Identical structures were observed in the dystrophic axons. Other organelles (RER, Golgi aparatus), while reduced in number, were without substantial alteration. Electron microscopy of dewaxed pontine samples (case 3) showed similar structures. The only difference was an increase of electron lucent space in the storage compartment leading to granulovacuolar neuronal cytology and an increase in the size of individual storage lysosomes, up to 1 μm in diameter on average. The ultrastructure differed from the ultrastructure of the lysosomes in the visceral storage cells  and from the lysosomes of the other known neurolysosomal storage disorders featured by membranous lipid deposits.
Biochemical analysis of residual lipids in FFPE samples from the pons (case 3, day 119) which were rich in ballooned granulovacuolar neurons, revealed a threefold to sixfold elevation of gangliosides (GM1, GM2, GM3 types), lactosylceramide and globotriaosylceramide as compared to the controls (data not shown). At this point we must note some limitations of the analysis caused by previous dehydrations, as well as the potential contribution (although minor) to the overall lipid content of non-neuronal storage elements present in the tissue.
In all the three cases the neuronal perikaryal storage granules displayed a uniform lysosomal immunophenotype, featured by strong staining for cathepsin D (luminal marker) and for the late endosomal/lysosomal membrane markers LAMP1, 2 (Figs. 1b, b,2c,2c, d). In the majority of storage neurons the perikaryal granules displayed variable positivity for the subunit c of mitochondrial ATP synthase (SCMAS) with the respective antibody (data not shown).
A peculiar feature of the immunophenotype was the nearly uniform, strong, granular immunostaining of ubiquitin (Fig. 4a–c), present in all analyzed samples (cortical, subcortical and extra cerebral). The cortical neurons in case 1 were ubiquitinated almost without any substantial difference between the individual layers. Axonal spheroids were ubiquitinated as well. The neurons of the peripheral nervous system (gut, lung, liver, kidney, and urinary bladder) displayed an identical lysosomal immunophenotype, including the high extent of ubiquitination (Fig. 4d). The cellular pattern of ubiquitination, seen in bright-field microscopy, was suggestive of its association with storage lysosomes (for details, see below).
To evaluate the proportion of ubiquitin protein conjugates (mono- and polyubiquitinated) in the overall ubiquitin signal, the antibodies (clone FK1 and FK2, Table 1) against these types of epitopes  were used. We were able to detect significant amounts of mono- and polyubiquitinated moieties (FK2 antibody, data not shown) with the same staining patterns as the above-described ubiquitin staining. Unfortunately, the FK1 antibody (polyubiquitinated protein conjugates) did not provide reliable staining in the control samples (Mallory bodies rich liver biopsy) and as such was not included in the study. The cortical neurons in age-matched controls were immunonegative for ubiquitin. The immunophenotype of storage lysosomes in all the affected non-neuronal cells, from the brain (astrocytes, microglial phagocytes) and the visceral region was identical to the neurolysosomes, except for the absence of any detectable ubiquitination (Fig. 4e).
The immunohistochemical detection of cytoplasmic aggresomal sequestered proteins using p62 antibody did not show any positivity in any of the evaluated cortical and subcortical brain samples of all the three cases (data not shown).
In contrast to pSap deficiency, neurolysosomal ubiquitination was undetectable in the following neurolysosomal storage disorders: Niemann–Pick disease type C1, type A (Fig. 4f), infantile sialic storage disorder, mucolipidosis type I, aspartylglucosaminuria, alpha-mannosidosis, polysulphatase deficiency, and glycogen storage disease type II. Only the axonal spheroids and the neuronal tangles, particularly numerous in protracted neuronopathic Niemann–Pick type C cases, displayed strong ubiquitination. In neuronal ceroid lipofuscinoses, types 2, 3, 4 and 8, the main population of storage granules was devoid of ubiquitination. The only exception was strong ubiquitination seen in a small population of transformed storage material present as globules or spheroids in the neuronal perikarya . Moderate ubiquitination of storage neurons has been seen in the group of mucopolysaccharidoses (types I–III). Extra cerebral non-neuronal storage cells in all the above-mentioned disorders lacked any detectable ubiquitination. We could not confirm improved ubiquitin immunostaining with the recommended pretreatment .
Multiple indirect immunofluorescence labeling experiments were performed on sections of the spinal cord (case 3) in order to evaluate the relationship between the detectable ubiquitin signals and the potentially involved, cellular compartments. Prior to the evaluation of the signals in confocal images, we performed image restoration based on deconvolution using the microscope’s measured PSF, a method known to increase the effective image resolution [35, 57, 64]. The characteristics of the signals in the evaluated images allowed us to apply the cross-correlation function (CCF) estimation  for the analysis of their spatial (colocalization) relationship. The CCF method of colocalization evaluation of complex staining patterns is advantageous because it does not require image segmentation and can discriminate positive, negative and non-correlating signals.
In general, the signals obtained by immunofluorescence labeling followed the patterns observed by immunohistochemical staining. The intensity of the ubiquitin signal was inversely correlated to the endoplasmic reticulum (ER) and mitochondrial signals among the evaluated neurons. This resulted in a population of neurons strongly positive for ubiquitin and almost negative for ER and mitochondrial signals. This feature could be documented by the distribution of Pearson’s coefficient values in the CCF plots (Fig. 5c, d). While this loss of epitope detectability in the presence of strong ubiquitin positivity was clear for the ER and mitochondrial epitopes, a similar phenomenon was not observed for the two late endosomal/lysosomal markers (LAMP2, CatD).
In addition, the double labeling of the mitochondrial epitopes and of the late endosomal/lysosomal membrane epitope (LAMP2) in search for lysosomes with entrapped mitochondria or for mitochondrial remnants did not provide clear evidence of such events. This was, most probably, due to the combination of diffraction limited resolution of the microscope and/or advanced degradation of the mitochondrial epitopes.
Figure 5 shows images of the selected neurons with the corresponding CCFs and their distribution for the above-mentioned immunofluorescence labeling. From the five evaluated labeling combinations, only the signals of ubiquitin and LAMP 2/cathepsin D showed a non-random distribution (colocalization) according to the CCF in the population of evaluated neurons (Fig. 5a, b). The full-width of the half maximum (FWHM) of the CCF curves should correspond to the diameter of the evaluated objects . This criterion stands for the median value of both the CCF curves representing the ubiquitin/LAMP2-CatD signals and corresponds to the diameter values obtained by electron microscopy. The characteristics of ubiquitin/LAMP2 and ubiquitin/cathepsin D CCF curves (FWHM or maximum Pearson’s coefficient values) did not allow unambiguous discrimination between the prevalence of the two phenomena i.e. ubiquitination of the late endosomal/lysosomal membranes or ubiquitination of the late endosomal/lysosomal contents. Despite this ambiguity, which is most likely caused by the resolution limit of the microscope, we were able to demonstrate the colocalization of the ubiquitin signal with the late endosomal/lysosomal cellular compartment in pSap deficient neurons. Analysis of the other staining combinations (anti-ubiquitin/anti-PDI, anti-ubiquitin/anti-60 kDa antigen of human mitochondria and anti-60 kDa antigen of human mitochondria/anti-LAMP2) yielded a wide distribution of values, ranging from random distributions to mild exclusion of the signals (negative values of the Pearson’s coefficient) (Fig. 5c–e). CCF found that for the anti-60 kDa antigen of human mitochondria/anti-LAMP2 (mitochondrial/lysosomal), staining could be regarded, in this case, as a positive control for a random/exclusion relationship of the signals.
A comparison of brain cortical neuropathology showed pronounced differences between case 1 and cases 2 and 3. The histology in case 1 revealed a dense population of cortical neurons without substantial numerical and structural deviation from age-matched controls. The cortical neurons were moderately affected by storage, with a gradual increase toward the deeper layers (Fig. 1a). The neuronal nuclei were mostly vesicular with well-discernible nucleoli. The process culminated in the neurons of the subcortical regions (thalamus and basal ganglia). The degree of astrocytosis and the number of microglial phagocytes were proportional to the degree of neuronal storage, i.e. it was minimal in the cortex (Fig. 1c, d). In cases 2 and 3 the cortical areas displayed a profound depletion of the neurons [13, 25] and the residual neurons were identified as finely granulated single cells or small groups of cells that were detectable by using the NeuN antibody. Instead of the normal neuronal architecture there was a dense cellular population composed of equal proportions of large, coarsely vacuolated, CD 68 positive phagocytic microglia and hyperplastic, GFAP positive astrocytes (Fig. 6). In the rest of the central nervous system, the neurons were not substantially reduced in amount. No signs of caspase 3 activation or other cytological features of apoptosis were present either in the cortical or the subcortical neurons in case 1 or in the neurons in cases 2 and 3 (data not shown).
In all the three cases there was a complete absence of pSap protein caused either by the nonsense-mediated decay of the gene transcript  or by the failure of the mRNA translation [13, 54]. The discussion is focused on the nature of neurolysosomal storage and the remarkable sensitivity of the cortical neurons to pSap deficiency.
Whereas lysosomes in non-neuronal cells were distended by a massive accumulation of a set of sphingolipids due to multiple sphingolipid hydrolase insufficiency, due to pSap deficiency, leading to the foamy appearance of the affected cells, the neurons expressed an appreciably different pathology. The neuronal pathology featured finely granular lysosomes containing condensed pleiomorphic inclusions. Besides the standard membrane (LAMP 1 and LAMP 2) and luminal (cathepsin D) markers, their distinct feature was an association with strong ubiquitination including a significant proportion of ubiquitin protein conjugates detected by specific antibodies. They were devoid of ceroidlipofuscin and the lipid storage was borderline or of a low degree. We consider it important that ubiquitination has been proved to be absent in non-neuronal storage cells and even in numerous microglial phagocytes. It was also absent in the bulk of other neurolysosomal storage disorders featured by storage of defined lipid or glycoconjugate substrates due to deficient enzyme catalytic activity or due to altered lipid trafficking (see also ). Thus, in contrast to the non-neuronal cells, the absence of pSap leads to a different pathology in the neurolysosomes.
It should be compared to processes featured by the lysosomally associated ubiquitination. Ubiquitination associated with neurolysosomes has been described in the granulovacuolar lesions seen in Alzheimer’s disease and in scrapie infected mice, both appear to be autophagic vacuoles . The ultrastructure of neurolysosomes in neuronal perikarya (Fig. 3) and axons in our cases of pSap deficiency resembled ultrastructural changes in the neuroaxonal dystrophy classified as a macroautophagy process  that also featured a high degree of ubiquitination [11, 42] combined with lysosomal enzyme activities .
In the cases of pSap deficiency we were able to document a positive correlation (colocalization) to ubiquitination and late endosomal/lysosomal markers as well as signs attributable to mitochondrial degradation (SCMAS detectability).
Ubiquitination has also been described as a part of the protein conjugation system of autophagosomal compartment [18, 38, 58, 59], a process dominated, however, by the homologs of yeast Atg ubiquitin-like proteins including mammalian LC3 protein [27, 28]. Unfortunately, the antibody against the LC3 autophagosomal membrane component provided ambiguous results in our FFPE tissues, partly due to the lack of appropriate reference samples; therefore we decided not to include these results. Ubiquitination of lysosomal contents has been repeatedly described [10, 36, 37, 41, 58] and explained by lysosomal sequestration of ubiquitin-tagged proteins.
We thus propose the existence of a similar mechanism in pSap deficiency, i.e. excessive lysosomal sequestration of the ubiquitin-tagged proteins released most probably from damaged neuronal membranes or resulting from impaired downstream pSap signaling [2, 23]. The previously demonstrated relationship of the ubiquitin/proteasome pathway and cytoplasmic vacuoles with non-lysosomal characteristics  does not correspond with our findings in pSap deficiency. The absence of immunodetectable p62 does not support the aggresomal-based ubiquitination  in pSap deficiency neuropathology, nevertheless, ubiquitination has been suggested to trigger an autophagocytosis process under certain conditions . In summary, our findings can be interpreted as an excessive influx of ubiquitinated biological material (either in bulk or as individual molecules) into the neurolysosomes. It represents features compatible with the process of autophagy, encompassing a range of both bulk (macro and micro types) and of its molecular variants, [8, 49, 53] which are difficult to distinguish in routinely processed FFPE samples. It is worth mentioning that the absence of neurotrophic factors was found to activate autophagocytosis, which may culminate in a specific type of programmed cell death (PCD II) [4, 59] or persist as an ongoing process . This supports our hypothesis that the specific neurolysosomal pathology in human pSap deficiency may be closely related to the absence of pSap´s trophic function.
The vulnerability of the cortical neurons to cell death in pSap deficiency is immense. The findings in the three presented cases suggest a critical inability of nearly the whole cortical neuronal population to survive after a certain postnatal time point. The subependymal germinal zone as well as the neuronal migration does not seem to be affected. This massive, stage dependant neuronal loss, most probably triggered by pSap absence, occurs within a time period of 60–80 days. With respect to the extent and relative abruptness of this phenomenon we would like to designate it as a cortical neuronal survival crisis. A similar phenomenon has never been described in any of the known neurolysosomal storage disorders, with the exception of infantile NCL1 and the recently described congenital NCL . In infantile NCL1, the profound neuronal cortical depopulation develops over several years , strongly contrasting with the early cortical neuronal survival crisis in pSap deficiency. The congenital NCL, caused by profound cathepsin D deficiency, is featured by extensive prenatal neuronal loss.
Unfortunately, brains from other cases of pSap deficiency [19, 66] were not available for study. The loss of neuronal survival capacity as described has been repeatedly reported as a consequence of neurotrophic factor deprivation leading to programmed cell death, mostly from the caspase independent (non-apoptopic) type [1, 9, 26, 29, 52]. The absence of detectable activated caspase 3 in our cases is in accord with it. It should be stressed that an amino acid sequence has been recognized in pSap [33, 48, 51] as being responsible for the neurotrophic activities in a variety of neural cells in vitro and in vivo, including differentiation, cell death prevention, regeneration [5, 24, 32, 33, 47, 55], and stimulation of myelin synthesis [7, 21, 22]. Cell death prevention by pSap has also been described in non-neuronal U937 monocytic cells [7, 44]. It has been postulated that unprocessed pSap, localized to both fetal and adult human neurons [15, 31], exerts its neurotrophic effect partly through a putative Go protein coupled receptor  and MAP kinase , and partly due to its unique affinity for glycosphingolipids, particularly gangliosides .
The above-mentioned data support the concept of pSap as having a crucial role in the survival of human cortical neurons and indicate that its absence may be critical for their survival in early postnatal life.
In this context it is worth noting that in the mouse pSap KO model [17, 50], the neurolysosomal storage starts around day 10 and 30 in spinal and cerebral neurons, respectively, and progresses rapidly to full blown glycolipid storage. As in human cases, storage is accompanied, by a high degree of neuronal ubiquitination. The neurological symptoms start on day 20. The animals do not survive beyond day 40. No signs of neuronal cortical depopulation have been described. These findings might point to the absence of a significant trophic effect of pSap on normal mouse neurons despite the fact that there is a strong postnatal increase in its mRNA .
Our results indicate that pSap deficiency in humans has different consequences with respect to the cell types affected. In non-neuronal cells, the disorder does not lead to any demonstrable trophic defect and is dominated by the biochemical sequels linked to the absence of Saps i.e. inactivation of multiple sphingolipid hydrolases. The resulting storage of undigested lipids markedly distends the lysosomal compartment. However, in the peripheral and central neurons, the consequences of pSap deficiency seem to be determined by the unique sensitivity of the neurons to the lack of a trophic effect of secreted unprocessed pSap. We speculate that the initial phase of the neurolysosomal process (in both brain and peripheral neurons) strongly resembles autophagocytosis, while lipid storage plays only a minor role. In the cortical neurons the process seems to be terminated after several weeks of life by massive cell death, which by exclusion corresponds most probably to the programmed cell death type II, followed by removal by microglial phagocytes. It appears likely that pSap is one of the trophic factors essential for survival, differentiation and maintenance of human neurons particularly in the early phases of brain development.
This work was supported by the research project MSM 0021620806 of the Ministry of Education, Youth and Sports of the Czech Republic.