Evolution of octopod sperm I: comparison of nuclear morphogenesis in Eledone and Octopus

Morphogenesis of the Eledone cirrhosa sperm nucleus, as studied by electron microscopic techniques, is compared with that of Octopus vulgaris. Both species of cephalopods belong to the family Octopodidae. The results indicate that extensive nuclear helicoidization during E. cirrhosa spermiogenesis is brought about by modifications of the function of structural components already present in the late steps of O. vulgaris spermiogenesis. In particular, changes in the regulation of perinuclear microtubule contraction in E. cirrhosa spermatids, as well as a decrease in basicity of protamines, promote nuclear helicoidization. Disulphide bond formation between protamine molecules fixes the completely helicoidal shape of the nucleus in mature sperm of E. cirrhosa.     

Spermatozoa of two Eledone species (Cephalopoda, Octopoda)

Spermatozoa from testes and spermatophores of two octopod species, Eledone cirrhosa and E. moschata, have been investigated by electron microscopy. At the base of the mature sperm acrosome of both species a well developed, periodic, conical structure is present. This structure is strikingly similar to that present in the Octopus sp. acrosome. Also the modalities of formation of such a structure during spermiogenesis show strong similarities between the Octopus and Eledone genera. The resistance to disruption of sperm chromatin of E. cirrhosa and E. moschata after treatments with SDS and mercaptoethanol which are known to dissolve disulfide-bridges, reveals the presence of S-S crosslinks.     

Crab and mollusc shell drilling by Octopus vulgaris (Mollusca: Cephalopoda) in the Ria de Vigo (north-west Spain)

Octopus vulgaris living in the Ria de Vigo, north-west Spain, sometimes drills a cavity in the carapace of crabs and shells of molluscs. These holes have features with the same characteristics as those made in molluscs by O. vulgaris and in crabs by Eledone cirrhosa when isolated in aquaria. This is the first report of drilling the carapace of crabs by Octopus vulgaris .     

C-terminal kinesin motor KIFC1 participates in acrosome biogenesis and vesicle transport

We have identified a possible role for the KIFC1 motor protein in formation of the acrosome, an organelle unique to spermatogenesis. KIFC1, a C-terminal kinesin motor, first appears on membrane-bounded organelles (MBOs) in the medulla of early spermatids followed by localization to the acrosomal vesicle. KIFC1 continues to be present on the acrosome of elongating spermatids as it flattens on the spermatid nucleus; however, increasing amounts of KIFC1 are found at the caudal aspect of the spermatid head and in distal cytoplasm. The KIFC1 motor is also found in the nucleus of very immature round spermatids just prior to its appearance on the acrosome. In some cases, KIFC1 appears localized just below the nuclear membrane adjacent to the subacrosomal membrane. We demonstrate that KIFC1 is associated with importin beta and colocalizes with this nuclear transport factor on curvilinear structures associated with the spermatid nuclei. These data support a model in which KIFC1, perhaps in association with nuclear factors, assists in the formation and/or elongation of the spermatid acrosome. This article represents the first demonstration of a direct association of a molecular motor with the spermatid acrosome, the formation of which is essential for fertilization.     

Dynamics of Sun5 Localization during Spermatogenesis in Wild Type and Dpy19l2 Knock-Out Mice Indicates That Sun5 Is Not Involved in Acrosome Attachment to the Nuclear Envelope

The acrosome is an organelle that is central to sperm physiology and a defective acrosome biogenesis leads to globozoospermia, a severe male infertility. The identification of the actors involved in acrosome biogenesis is therefore particularly important to decipher the molecular pathogeny of globozoospermia. We recently showed that a defect in the DPY19L2 gene is present in more than 70% of globozoospermic men and demonstrated that Dpy19l2, located in the inner nuclear membrane, is the first protein involved in the attachment of the acrosome to the nuclear envelope (NE). SUN proteins serve to link the nuclear envelope to the cytoskeleton and are therefore good candidates to participate in acrosome-nucleus attachment, potentially by interacting with DPY19L2. In order to characterize new actors of acrosomal attachment, we focused on Sun5 (also called Spag4l), which is highly expressed in male germ cells, and investigated its localization during spermatogenesis. Using immunohistochemistry and Western blot experiments in mice, we showed that Sun5 transits through different cellular compartments during meiosis. In pachytene spermatocytes, it is located in a membranous compartment different to the reticulum. In round spermatids, it progresses to the Golgi and the NE before to be located to the tail/head junction in epididymal sperm. Interestingly, we demonstrate that Sun5 is not, as initially reported, facing the acrosome but is in fact excluded from this zone. Moreover, we show that in Dpy19l2 KO spermatids, upon the detachment of the acrosome, Sun5 relocalizes to the totality of the NE suggesting that the acrosome attachment excludes Sun5 from the NE facing the acrosome. Finally, Western-blot experiments demonstrate that Sun5 is glycosylated. Overall, our work, associated with other publications, strongly suggests that the attachment of the acrosome to the nucleus does not likely depend on the formation of SUN complexes.     

Acrosome formation in Ceratitis capitata (Diptera, Tephritidae)

The stages of morphogenesis of the acrosome of Ceratitis capitata are well defined. This organelle is formed by the Golgi complex and, as it matures, takes up a position laterally in relation to the anterior region of the sperm nucleus. An interstitial membrane marks the area of contact between nucleus and acrosome in the spermatid, and is found even in mature sperm cells. The acrosome contains hydrolytic enzymes, as detected by acid phosphatase reaction.     

Energy balance and cold adaptation in the octopus Pareledone charcoti

A complete energy balance equation is calculated for the Antarctic octopus Pareledone charcoti at 0 degrees C. Energy used in respiration, growth, and excretion of nitrogenous and faecal waste, was recorded along with the total consumption of energy through food, for three specimens of P. charcoti (live weights: 73, 51 and 29 g). Growth rates were very slow for cephalopods, with a mean daily increase in body weight of only 0.11%. Assimilation efficiencies were high, between 95.4 and 97.0%, which is consistent with previous work on octopods. The respiration rate in P. charcoti was low, with a mean of 2.45 mg O(2) h(-1) for a standard animal of 150 g wet mass at 0 degrees C. In the North Sea octopus Eledone cirrhosa, respiration rates of 9.79 mg O(2) h(-1) at 11.5 degrees C and 4.47 mg O(2) h(-1) at 4.5 degrees C for a standard animal of 150 g wet mass were recorded. Respiration rates between P. charcoti and E. cirrhosa were compared using a combined Q(10) value between P. charcoti at 0 degrees C and E. cirrhosa at 4.5 degrees C. This suggests that P. charcoti are respiring at a level predicted by E. cirrhosa rates at 4.5 and 11.5 degrees C extrapolated to 0 degrees C along the curve Q(10)=3, with no evidence of metabolic compensation for low temperature.     

泥螺精子发生的超微结构研究

利用透岸民镜观察了泥螺精子发生的过程。结果表明;泥螺精子发生经历了一系列重要的形态和结构变化,主要有核逐渐延长,染色质浓缩,顶体形成,线粒体逐步发达与融合,胞质消除及鞭毛的形成等。泥螺精细胞分化可分为3个时期,在精细细胞分化过程中,细胞核形态及染色质的变化与其他软体动物有较大的差异,核内椭圆形到肾形,再变化为长圆柱形;染色质由絮状颗粒变为细纤维丝状,再变为长纤维丝状,最后向高电子密度均质状态转变,初步探讨了泥螺精子发生过程中核及细胞器的超微结构变化在分类上的意义。     

Studies on the fine structure of spermatids and spermatozoa of the crab, Pinnixia sp

Early spermatids of the carb, Pinnixia sp., are characterized by a large nuclear/cytoplasmic ratio. During early spermiogenesis an organelle, composed of pentalaminar membranes derived from the endoplasmic reticulum and nuclear membranes, is formed. Portions of this organelle become incorporated within a cylinder-shaped invagination of the acrosome. Portions of the nuclear membrane disappear beneath the acrosome resulting in intermingling of nucleoplasm, centrioles and mitochondria. The nuclear membrane elsewhere is found as a pentalaminar membrane underlying the plasma membrane. Centrioles are found in mature spermatozoa at the base of the cylinder-shaped acrosomal invagination, and mitochondria are found intermingled with nuclear remanants surrounding the acrosome. This datum is compared to previously described events in spermiogenesis of other decapod crustacea and arthropods exhibiting similar modes of spermiogenesis. It is concluded that the differences and/or similarities exhibited by centrioles and mitochondria in these forms could be significant in terms of subsequent zygote differentiation.     

Chromatin organization during spermiogenesis in Octopus vulgaris. I: Morphological structures

In the process of the chromatin remodeling that occurs during spermiogenesis in some animal species, it is possible to distinguish between two separate aspects: the chromatin condensation pattern itself (granular, fibrillar, or lamellar), and the architecture of this pattern, that is to say, its arrangement within the nucleus. In the cephalopod Octopus vulgaris these two aspects are clearly differentiated. The condensation pattern develops from 25 nm fibers to fibers with a tubular aspect and with a progressively increasing diameter (40-60 nm and then to 80 nm), to end finally in the form of very thin fibers (3-5 nm) product of the coalescence and dissolution of the major fibers. The main directive force that governs this process lies in the global change that occurs in the proteins that interact with all (or the major part) of the genomic DNA. The condensation pattern by itself in this species does not present a fixed order: most of the fibers appear without any predominant spatial direction in the spermiogenic nuclei. However, as the nuclei elongate, the chromatin fibers arrange in parallel following the elongation axis. This parallel disposition of the chromatin fibers appears to be mediated by two specific areas, each of which we call a "polar nuclear matrix" (PNM). These matrices differentiate in the basal and apical nuclear poles adjacent to the centriolar implantation fosse and the acrosome, respectively. The areas that constitute the PNM have the following characteristics: (a) they are the only areas where DNA is found anchored to the nuclear membrane; (b) they are the zones from which the chromatin condensation pattern (fibers/tubules) begins; and (c) they are most probably the points through which the mechanical forces originating from nuclear elongation are transmitted to chromatin, causing the chromatin fibers/tubules to adopt an almost perfectly parallel disposition. Finally, we discuss the importance of the architecture of the chromatin condensation pattern, as it is one of the determining factors of the spatial organization of the mature sperm genome and chromosome positioning.     

The cardiac innervation of Eledone cirrhosa (Lamarck) (Mollusca: Cephalopoda)

The innervation to the cardiac organs and vessels of the octopods Eledone cirrhosa, E. moschata and Octopus vulgaris is described from vitally stained fresh material and wax-embedded sections. This innervation arises from the paired visceral nerves and includes two main peripheral ganglia (fusiform and cardiac) on each side. Several new details of the innervation are reported. Nerves supplying the lateral venae cavae arise from the ventricular nerves at the level of the ventricle. Nerve fibres run to the efferent branchial vessels from the cardiac ganglia. A small ganglion, lying on the auriculo-ventricular nerve, is described for some specimens of both species of Eledone, and is named the auricular ganglion. Commissural strands linking the right and left ventricular nerves of either side are found in Eledone, comparable to those previously described from Octopus. The detailed branching pattern of the innervation shows considerable individual variation and consistent interspecific differences. In E. cirrhosa the fine fibres innervating the inner and outer muscle layers of the auricle show distinct differences in their configuration. Innervation at the surface of the ventricular lumen and around the coronary arterial vessels shows evidence of specialization. The muscle of the branchial heart, particularly the valve leaflets at the junction of the heart and the lateral vena cava, is abundantly innervated. The observations are discussed in relation to other cephalopods and to their probable physiological significance. It is suggested that they provide evidence for a greater degree of neural influence in the control of the cardiac organs than is usually supposed and that they support the idea that the lateral venae cavae have a significant role in the generation of circulatory pressures.     

Ultrastructure of spermiogenesis in the American alligator,Alligator mississippiensis (Reptilia,Crocodylia, Alligatoridae)

Testicular samples were collected to describe the ultrastructure of spermiogenisis in Alligator mississipiensis (American Alligator). Spermiogenesis commences with an acrosome vesicle forming from Golgi transport vesicles. An acrosome granule forms during vesicle contact with the nucleus, and remains posterior until mid to late elongation when it diffuses uniformly throughout the acrosomal lumen. The nucleus has uniform diffuse chromatin with small indices of heterochromatin, and the condensation of DNA is granular. The subacrosome space develops early, enlarges during elongation, and accumulates a thick layer of dark staining granules. Once the acrosome has completed its development, the nucleus of the early elongating spermatid becomes associated with the cell membrane flattening the acrosome vesicle on the apical surface of the nucleus, which aids in the migration of the acrosomal shoulders laterally. One endonuclear canal is present where the perforatorium resides. A prominent longitudinal manchette is associated with the nuclei of late elongating spermatids, and less numerous circular microtubules are observed close to the acrosome complex. The microtubule doublets of the midpiece axoneme are surrounded by a layer of dense staining granular material. The mitochondria of the midpiece abut the proximal centriole resulting in a very short neck region, and possess tubular cristae internally and concentric layers of cristae superficially. A fibrous sheath surrounds only the axoneme of the principal piece. Characters not previously described during spermiogenesis in any other amniote are observed and include (1) an endoplasmic reticulum cap during early acrosome development, (2) a concentric ring of endoplasmic reticulum around the nucleus of early to middle elongating spermatids, (3) a band of endoplasmic reticulum around the acrosome complex of late developing elongate spermatids, and (4) midpiece mitochondria that have both tubular and concentric layers of cristae. J. Morphol., 2010. © 2010 Wiley‐Liss, Inc.     

Maturation of mammalian spermatozoa: modifications of the acrosome and plasma membrane leading to fertilization

The mammalian spermatozoon is a terminally differentiated cell. Its surface is covered by a continuous plasma membrane that is divided into distinct domains in which functional molecules are distributed. The acrosome is an internal organelle located at the anterior head and contains hydrolytic enzymes. The anterior acrosome participates in the acrosome reaction, which is an indispensable event during fertilization. These surface domains and the acrosome are formed during spermiogenesis, during which associated molecules are transported and organized. Many of the molecules thus arranged are functionally immature but gradually become mature during epididymal maturation. Some of them are further altered and redistributed during the fertilization process and play various roles. Here, the sequential changes in the acrosome and plasma membrane during spermatozoan maturation are reviewed, particular attention being paid to molecules derived from the testis.     

Localization of the ribosomal protection protein Tet(O) on the ribosome and the mechanism of tetracycline resistance

Tet(O) belongs to a class of ribosomal protection proteins that mediate tetracycline resistance. It is a G protein that shows significant sequence similarity to elongation factor EF-G. Here we present a cryo-electron microscopic reconstruction, at 16 A resolution, of its complex with the E. coli 70S ribosome. Tet(O) was bound in the presence of a noncleavable GTP analog to programmed ribosomal complexes carrying fMet-tRNA in the P site. Tet(O) is directly visible as a mass close to the A-site region, similar in shape and binding position to EF-G. However, there are important differences. One of them is the different location of the tip of domain IV, which in the Tet(O) case, does not overlap with the ribosomal A site but is directly adjacent to the primary tetracycline binding site. Our findings give insights into the mechanism of tetracycline resistance.     

The Calcium-mobilizing Messenger Nicotinic Acid Adenine Dinucleotide Phosphate Participates in Sperm Activation by Mediating the Acrosome Reaction

Before a sperm can fertilize an egg it must undergo a final activation step induced by the egg termed the acrosome reaction. During the acrosome reaction a lysosome-related organelle, the acrosome, fuses with the plasma membrane to release hydrolytic enzymes and expose an egg-binding protein. Because NAADP (nicotinic acid adenine dinucleotide phosphate) releases Ca²⁺ from acidic lysosome-related organelles in other cell types, we investigated a possible role for NAADP in mediating the acrosome reaction. We report that NAADP binds with high affinity to permeabilized sea urchin sperm. Moreover, we used Mn²⁺ quenching of luminal fura-2 and ⁴⁵Ca²⁺ to directly demonstrate NAADP regulation of a cation channel on the acrosome. Additionally, we show that NAADP synthesis occurs through base exchange and is driven by an increase in Ca²⁺. We propose a new model for acrosome reaction signaling in which Ca²⁺ influx initiated by egg jelly stimulates NAADP synthesis and that this NAADP acts on its receptor/channel on the acrosome to release Ca²⁺ to drive acrosomal exocytosis.     

Hole boring of crustacean prey by the octopus Eledone cirrhosa (Mollusca, Cephalopoda)

Eledone cirrhosa has been found to make a borehole in the carapace of a high proportion of its crustacean prey. This is the first account of drilling in crustaceans by octopus. The frequency of incidence of the boring behaviour varied between prey species from 17 to 93% of those killed. The incidence of boreholes was higher in crabs killed by small octopuses. Using crabs mainly of the genera Cancer, Carcinus, Corystes and Macropipus , the distribution and orientation of the boreholes was recorded. The boreholes occurred in any part of the carapace but the great majority were found close to the mid-line and in the posterior half. The long axis of the oval penetration was usually aligned with the anteroposterior axis of the crab. The Mediterranean species Eledone moschata was also found to bore crabs, and newly hatched juveniles of this species are capable of boring as early as their second killing of a live crab. No evidence was found that Octopus vulgaris normally bores the carapace of crabs.     

Real-time observation of acrosomal dispersal from mouse sperm using GFP as a marker protein.

We produced transgenic mouse lines that accumulate mutated green fluorescent protein (EGFP) in sperm acrosome, a membrane limited organelle overlying the nucleus. The sperm showed normal fertilizing ability and the integrity of their acrosome was easily examined in a non-invasive manner by tracing the GFP in individual 'live' sperm with fluorescent microscopy. The time required for the dispersal of acrosomal contents was demonstrated to be approximately 3 s after the onset of acrosome reaction.     

Influence of Auxin on Young's Modulus in Stems and Roots of Pisum and the Theory of Changing the Modulus in Tissues

The effect of auxin on elastic extensibility has been investigated by means of the resonance frequency melhod in Pisum, sativum. The time lag for the decrease in Young's modulus E, caused by IAA, was between 2 and 3 minutes in etiolated stem internodes. The time lag for growth was about 7 minutes. The measurements of E in root segments were only qualitative owing to the structural characteristics; IAA decreases E in roots as it does in stems, but only in the region where IAA is assumed to enhance elongation. The connexion between elastic modulus and growth is discussed with reference to other investigations. The assumption has been made that a decrease in elastic modulus indicates a change in the cell wall which in some way is conducive to growth (induction of elongation). The theoretical possibilities of changing E have been discussed with reference to the formula for water fluxes. Both a change in a cell wall properly and a change in the cytoplasmic permeability are able to cause a change in E in the same way as auxin does. An early action of auxin must be located in the cell-wall-plasmalemma region.     

The axoneme is involved in the elongation of the spermatid nucleus of Drosophila subobscura

Summary

Our analysis of spermiogenesis of Drosophila subobscura indicates that the axoneme takes part in the elongation of the spermatid nucleus, as follows. In sperm of D. subobscura the axoneme accompanies the nucleus in its full length up to the acrosome. Before the elongation of the nucleus begins, the centriole contacts the nuclear membrane, and is orientated with its axis to the centre of the spherical nucleus. Later in development, at the beginning of nucleus elongation, the axis of the centriole does no longer point to the centre of the nucleus but is dislocated more to one side of the nucleus. Subsequently, the axoneme which is growing from the centriole, pushes the nucleus which develops a cap-like structure over the anterior end of the centriole. By the continuosly growing axoneme stretching forces are applied to the anterior part of the nucleus. Consequently the elongating nucleus gets a smaller diameter anteriorly than posteriorly. And the longer the total length of the sperm is the longer is the nucleus. During elongation the chromatin shows a network-like structure. Nucleus elongation stops when the chromatin is fully condensed but the axoneme continues to grow. Thereupon the cap is no longer seen, and the anterior part of the nucleus which previously was the cap, forms now a bulge beside the centriole and the axoneme.     

Assembly of spermatid acrosome depends on microtubule organization during mammalian spermiogenesis

The acrosome is a secretory vesicle attached to the nucleus of the sperm. Our hypothesis is that microtubules participate in the membrane traffic between the Golgi apparatus and acrosome during the first steps of spermatid differentiation. In this work, we show that nocodazole-induced microtubule depolarization triggers the formation of vesicles of the acrosomal membrane, without detaching the acrosome from the nuclear envelope. Nocodazole also induced fragmentation of the Golgi apparatus as determined by antibodies against giantin, golgin-97 and GM130, and electron microscopy. Conversely, neither the acrosome nor the Golgi apparatus underwent fragmentation in elongating spermatids (acrosome- and maturation-phase). The microtubule network of round spermatids of azh/azh mice also became disorganized. Disorganization correlated with fragmentation of the acrosome and the Golgi apparatus, as evaluated by domain-specific markers. Elongating spermatids (acrosome and maturation-phase) of azh/azh mice also had alterations in microtubule organization, acrosome, and Golgi apparatus. Finally, the spermatozoa of azh/azh mice displayed aberrant localization of the acrosomal protein sp56 in both the post-acrosomal and flagellum domains. Our results suggest that microtubules participate in the formation and/or maintenance of the structure of the acrosome and the Golgi apparatus and that the organization of the microtubules in round spermatids is key to sorting acrosomal proteins to the proper organelle.