Thin Layer Of Connective Tissue Research Articles

Ethanol-induced Coma after Therapeutic Ethanol Injection of a Hepatic Cyst

Ethanol-induced Coma after Therapeutic Ethanol Injection of a Hepatic Cyst

REFINEMENT OF THE EXTRADURAL ANTERIOR CLINOIDECTOMY

Extradural removal of the anterior clinoid process is technically challenging because of the limited exposure. In our study of the extradural anterior clinoidectomy, we describe anatomic details and landmarks to facilitate sectioning of the orbitotemporal periosteal fold and elevation of the temporal fossa dura from the superior orbital fissure. We assess the morbidity associated with these procedures as well as compare the indications, advantages, and disadvantages of intra-versus extradural clinoidectomy. Of five formalin-fixed cadaveric heads, four were used for cadaveric dissections and one was used for histological examination. Sectioning of the orbitotemporal periosteal fold revealed a cleavage plane between the temporal fossa dura and a thin layer of connective tissue that covers the superior orbital fissure. The lacrimal nerve coursed immediately medial to this surgically created cleavage plane. The superior orbital vein crossed laterally under the cranial nerves, which pass through the superior orbital fissure. This vein is particularly vulnerable as it is composed only of endothelium and a basal membrane. Both intra- and extradural techniques for anterior clinoidectomy are important parts of the neurosurgical armamentarium. Sharp incision of the orbitotemporal periosteal fold to increase the extradural exposure of the anterior clinoid process should be made at the level of the sphenoid ridge and restricted to the periosteal bridge. Subsequent blunt elevation of the temporal fossa dura should be performed; however, peeling of the temporal fossa dura should be limited to avoid cranial nerve morbidity.

RETRACTED: The periosteum: Part 1: Anatomy, histology and molecular biology

The periosteum is a thin layer of connective tissue that covers the outer surface of a bone in all places except at joints (which are protected by articular cartilage). As opposed to bone itself, it has nociceptive nerve endings, making it very sensitive to manipulation. It also provides nourishment in the form of blood supply to the bone. The periosteum is connected to the bone by strong collagenous fibres called Sharpey's fibres, which extend to the outer circumferential and interstitial lamellae of bone. The periosteum consists of an outer "fibrous layer" and inner "cambium layer". The fibrous layer contains fibroblasts while the cambium layer contains progenitor cells which develop into osteoblasts that are responsible for increasing bone width. After a bone fracture the progenitor cells develop into osteoblasts and chondroblasts which are essential to the healing process. This review discusses the anatomy, histology and molecular biology of the periosteum in detail.

Lack of fibulin-3 causes early aging and herniation, but not macular degeneration in mice

A mutation in the EFEMP1 gene causes Malattia Leventinese, an inherited macular degenerative disease with strong similarities to age-related macular degeneration. EFEMP1 encodes fibulin-3, an extracellular matrix protein of unknown function. To investigate its biological role, the murine Efemp1 gene was inactivated through targeted disruption. Efemp1(-/-) mice exhibited reduced reproductivity, and displayed an early onset of aging-associated phenotypes including reduced lifespan, decreased body mass, lordokyphosis, reduced hair growth, and generalized fat, muscle and organ atrophy. However, these mice appeared to have normal wound healing ability. Efemp1(-/-) mice on a C57BL/6 genetic background developed multiple large hernias including inguinal hernias, pelvic prolapse and protrusions of the xiphoid process. In contrast, Efemp1(-/-) mice on a BALB/c background rarely had any forms of hernias, indicating the presence of modifiers for fibulin-3's function in different mouse strains. Histological analysis revealed a marked reduction of elastic fibers in fascia, a thin layer of connective tissue maintaining and protecting structures throughout the body. No apparent macular degeneration associated defects were found in Efemp1(-/-) mice, suggesting that loss of fibulin-3 function is not the mechanism by which the mutation in EFEMP1 causes macular degeneration. These data demonstrate that fibulin-3 plays an important role in maintaining the integrity of fascia connective tissues and regulates aging.

China rose (Hibiscus rosasinensis) petals: a potent natural carotenoid source for goldfish (Carassius auratus L.)

Goldfish (Carassius auratus) are in demand in world markets due to their attractive golden colour. Carotenoids are the primary source of colour in the skin of fish. To optimize the colour in captivity, fish must obtain an adequate level of carotenoids in their feed. With this objective, four natural colour enhancers were tested. A common batch of feed was divided into five equal portions and colour ingredients, spirulina (D-S), china rose petals (D-C), marigold petals (D-M) and Lactobacil, a commercial probiotic (D-L), were added at 5 mg kg−1 to four portions of feed; one portion (D-O) was kept as a control without any additive. A feeding trial was conducted for 8 weeks. Each 70 L aquarium was stocked with 10 fish (average weight 1.6 g) and feed was given at 5% of the body weight. Growth rate, survival, biochemical composition and pigmentation in the skin of fish were measured. Histological studies of gonads were also conducted. Growth of fish in different treatments was significantly different. There was no difference in the proximate composition of the fish at the start of the experiment but after 8 weeks of feeding, fish fed the diet supplemented with china rose petals had a lower moisture content (70.48%) and higher protein (17.7%) and lipid (5.25%) levels than the group fed the control diet. Pigmentation was the highest (4.01 μg g−1) in D-C, followed by D-M (3.16 μg g−1), D-S (2.92 μg g−1) and D-L (2.84 μg g−1) and the lowest (0.24 μg g−1) in D-O. Gonad development of fish fed with the D-C diet was better compared with the gonads of control (D-O) fish, followed by D-M-, D-L- and D-S-fed fish. Gonads of fish, fed D-C, showed well-marked changes in the testis where a large number of seminiferous tubules bound together by means of a thin layer of connective tissue were observed. These tubules were highly convoluted and were separated from each other by thin connective tissue stroma. The intra space contained connective tissue, blood capillaries and interstitial cells. The spermatogonia could be seen as a large spherical cell containing a large central nucleus with a distinct nucleolus. The study shows that the china rose (Hibiscus rosasinensis) petal is a potent natural carotenoid source for goldfish to enhance its colour and also accelerate gonadal development.

The arrangement and function of octopus arm musculature and connective tissue

The morphology of the musculature and connective tissues of the arms of Octopus bimaculoides was analyzed with light microscopy. We also studied O. briareus and O. digueti, which possess relatively more elongate and less elongate arms, respectively. The morphology of the arms was found to be remarkably uniform among species. The arms consist of a densely packed three-dimensional arrangement of muscle fibers and connective tissue fibers surrounding a central axial nerve cord. Three primary muscle fiber orientations were observed: 1) transverse muscle fibers oriented in planes perpendicular to the long axis of the arm; 2) longitudinal muscle fibers oriented parallel to the long axis; and 3) oblique muscle fibers arranged in helixes around the arm. The proportion of the arm cross section occupied by each of these muscle fiber groups (relative to the total cross sectional area of the musculature) remains constant along the length of the arm, even though the arm tapers from base to tip. A thin circular muscle layer wraps the arm musculature on the aboral side only. Much of this musculature has its origin and insertion on several robust connective tissue sheets including a layer surrounding the axial nerve cord and crossed-fiber connective tissue sheets located on the oral and the aboral sides of the arm. An additional thin layer of connective tissue wraps the arm musculature laterally and also serves as a site of origin and insertion of some of the muscle fibers. The fibers of the oral and aboral crossed-fiber connective tissue sheets are arranged oblique to the long axis of the arm with the same fiber angle as the oblique muscle layers that originate and insert on the sheets. The oblique muscle layers and the crossed-fiber connective tissue sheets thus form composite right- and left-handed helical fiber arrays. Analysis of arm morphology from the standpoint of biomechanics suggests that the transverse musculature is responsible for elongation of the arms, the longitudinal musculature is responsible for shortening, and the oblique muscle layers and associated connective tissues create torsion. Arm bending may involve unilateral contraction of longitudinal muscle bundles in combination with resistance to arm diameter increase due to contraction of the transverse musculature or passive stiffness of the arm tissues. The arms may also be bent by a combination of decrease in diameter due to contraction of the transverse musculature and maintenance of constant length on one side of the arm by unilateral activity of longitudinal muscle bundles. An increase in flexural stiffness of the arm may be achieved by cocontraction of the transverse and longitudinal muscle. Torsional stiffness may be increased by simultaneous contraction of both the right- and left-handed oblique muscle layers.

Plastic repair of the deferent duct with a silicone tubular prosthesis under conditions of a chronic experiment on laboratory animals

A connective tissue capsule consisting of a thin layer of the connective tissue envelopes the prosthesis by the end of week 1 after replacement of a part of the deferent duct with a silicone tubular prosthesis under conditions of a chronic experiment. By days 17-20 postoperation, two layers are clearly differentiated in the capsule: the outer layer consisted of a thin layer of connective tissue and the inner one consisted of compact connective tissue. The space between the silicone prosthesis and the connective tissue capsule is filled with the seminal fluid. Obturation of the deferent duct forms because of formation of internal spermatogranulomas and atypical growth of the deferent duct epithelium adhering to the prosthesis wall.

An ultrastructural study of connective tissue in mollusc integument III: Cephalopoda

We studied structure and ultrastructure of the subepidermal connective tissue (SEC) of the integument of three cephalopods ( Sepia officinalis, Octopus vulgaris and Loligo pealii). In all species, three distinct regions of the SEC were recognised: (a) an outer zone (OZ) that included the dermal–epidermal junction, and consisted of a thin layer of connective tissue containing muscles, (b) an extensive middle zone (MZ) containing a compact network of collagen fibres and numerous cells, (c) an inner zone (IZ) of loose connective tissue that merged with muscular fascia. This arrangement differs from that in bivalves and gastropods and recalls vertebrate integument. The dermal–epidermal junction of cephalopods differed from that of bivalves, gastropods and mammals in that the epidermal cells did not possess hemidesmosomes, and their intermediate filaments terminated directly in the plasmamembrane. The thick (120–500 nm) basal membrane (BM) had a superficial zone containing a regular array of granules; a lamina densa composed of a compact network of small filaments and granules; and an IZ distinguished by expansions of granular material protruding into underlying structures. Collagen fibres contained fibroblast-derived cytoplasmic thread, running through their centres and were surrounded by granular material that joins them to adjacent fibres. The collagen fibrils were of medium diameter (30–80 nm) had the typical ultrastructure of fibrillar collagens, and were surrounded by abundant interfibrillar material. The hypodermis was loose, with a network of small bundles of collagen fibrils. Cephalopod integument appears to represent a major evolutionary step distinguishing this class of molluscs.

Anatomy and physiology of the prostate and benign prostatic hyperplasia

The prostate is the shape of an inverted pyramid and lies between the urinary bladder and the pelvic floor. The base is the superior surface and lies at the bladder neck. The anterior border forms the posterior wall of the retropubic space and is attached to the pubic bones by the puboprostatic ligaments. The posterior surface is anterior to the rectum, and the inferolateral surfaces are surrounded by the puboprostaticus fibres of the levator ani muscle. The ejaculatory ducts pass through the posterior surface just inferior to the bladder and open into the prostatic urethra about halfway along its length. It is a fibromuscular and glandular organ that surrounds the prostatic urethra, the fibromuscular element being in direct continuity with the detrusor muscle of the bladder. The true capsule of the prostate is a thin layer of connective tissue at the periphery of the gland. This is surrounded by a condensation of pelvic fascia known as the false capsule. The main blood supply is from the prostatic branch of the inferior vesical artery. The venous drainage is via a plexus between the two capsules. Lymph vessels drain to the internal iliac nodes (Fig. 1).

The histological observations on the large intestine of the goose (Anser anser) during the pre- and post-hatching periods.

The development of the cecum and colon in the goose was investigated during the period from the 15th to 28th day of the incubation and from 1 to 30 days of age after hatching by light microscopy. By day 15 of the incubation, in the cecum and colon, the lumen was surrounded by pseudostratified epithelium. The previllous ridges appeared at 15th and 17th days of the incubation in the colon and ceca, respectively. At the base of previllous ridges, the epithelium changed into a simple prismathic epithelium at 15th and 17th days of the incubation in the colon and cecum, respectively. The villi appeared at the 21st days of the incubation. The crypts and goblet cells appeared on the first day after hatching. In the pre-hatching period, the lamina muscularis mucosa was present only in the colon. The submucosa consisted of loosely aggregated connective tissue in the pre-hatching period. In the post-hatching period, it consisted of a very thin layer of connective tissue. Its presence was only obvious where the cells of the submucosal nerve plexus or occasional large blood vessels considerably increased its thickness. The nerve plexus corresponding to the Auerbach's plexus of the mammalian intestine and submucosal nerve plexus appeared by 15th days of the incubation. From the 15th to 28th day of incubation, the tunica muscularis consisted of circular smooth muscle cells in the ceca. On the 28th day of the incubation a thinner longitudinal muscle layer added to the circular muscle layer. In the colon there was an outer longitudinal and a thicker circular muscle layer.

Light and scanning electron microscopic studies of the angioarchitecture of intrinsic muscle fibers of the anterior rat tongue.

Histological and scanning electron microscopy (SEM) characteristics of the microvasculature of muscle fibers in the anterior third of the adult rat tongue are described. For light microscopy, the specimens were embedded in paraffin and frontal sections were stained with Picro-Sirius. Thick sections were obtained from Spurr embedded samples and stained with toluidine blue solution. For SEM, specimens were obtained by the corrosion cast method and fractured specimens in dimethyl sulfoxide were observed with high-resolution SEM (HRSEM). The blood vessels, enveloped with a thin layer of connective tissue, had fibers running parallel to the muscular fibers. Capillary arterioles were noted following the endomysium, but their lateral branches often ran at right angles to the fibers. The capillary beds were clearly revealed in transverse sections where the individual capillaries appeared ring-like or elliptical in shape. The nuclei of endothelial cell cores could be seen on the vessel surfaces. Collagen fibers type I and III were noted in the connective tissue and in the fibrous layer of vessels.

Spontaneous early exposure of submerged implants: III. Histopathology of perforated mucosa covering submerged implants.

Spontaneous early exposure of dental implants could interfere with the early healing phase of dental implants. These exposures have been clinically classified according to degree of implant exposure from 0 (intact mucosa) to IV (complete exposure). The characteristics of perforated mucosa (Class I and II) covering submerged dental implants were examined histologically in this study. Biopsy specimens of 34 Class I and II perforated mucosa covering submerged dental implants were examined histologically. Serial sections were evaluated from the periphery of the specimen to the center of each perforation lesion. Class I specimens presented hyperplastic epithelium characterized by hyperparakeratosis and acanthosis. Chronic inflammatory cells diffusely infiltrated the connective tissue. Sections closer to the perforation revealed gradual epithelial invagination; in the deepest aspect, there was a cyst-like structure in all Class I specimens examined. A thin layer of connective tissue containing necrotic material and debris formed the "cystic" wall proximal to the implant cover screw. Class II specimens presented the same epithelial patterns; however, the cystic structures were replaced by direct contact between the cover screw and the oral cavity via the perforation. Spontaneous early perforations are the sequela of either traumatic irritation or failure of the tissue flaps to produce primary healing. Most Class I perforations include epithelial invagination and the formation of a cyst-like structure. Necrosis of the base of the "cyst" or enlargement of the perforation results in direct communication between the oral cavity and the covering screw surface (Class II).

Efectos producidos por Spinitectus jamundensis (Nematoda, Cystidicolidae) en el estómago del sábalo, Prochilodus lineatus (Pisces, Prochilodidae)

The presence of the nematode Spinitectus jamundensis in cardial and pyloric regions of the stomach of Prochilodus lineatus is observed. Samples of the parasitized stomach were analyzed by histological techniques using Hematoxilin-Eosin and Mallory (Azan) Heidenhain's stainnigs. The macroscopical description of the inner surface of the stomach showing damages in the parasites penetration sites, were observed. Histological observations show that the parasite enters the mucous membrane reaching muscular mucous membrane of the cardial region or the epithelial plaits in the pyloric region reaching up to the muscular layer without crossing it. In this way, the parasite remains confined by a thin layer of connective tissue and in almost direct contact with tissue liquids. Sometimes, in host tissues as response to the parasite presence, an increased level in the amount of lymphocytes in the surrounding tissues is observed.

3-D characterization of ganglion cells of the terminal nerve plexus of rat atrioventricular junction

Three-dimensional (3-D) morphology of neurons of the terminal nerve plexus of the atrioventricular junction was examined in a scanning electron microscope. Distributions of different cell types encountered as well as their relations to different structures of the atrioventricular specialized tissue were also studied. Most neurons were found disseminated in a thin connective tissue layer separating different segments of the atrioventricular conductive tissue from the interventricular septum. Sometimes, they formed small pluricellular ganglia (up to 5 neurons) but, frequently, they occurred isolated in the terminal ramifications of the intramural nerve plexus of specialized tissue. Some intranodal neurons could also be identified. According to their 3-D morphology, nerve cells of the perinodal ganglionated plexus could be divided into three categories: (1) Large unipolar neurons were scattered throughout the atrioventricular junction. Their long and thin axonal projections were often directed towards the interventricular septum. (2) Large pseudounipolar or bipolar neurons were located at a few specific loci, namely all along the bundle of His and its bifurcation into the right and left bundle branches. Frequently, they occurred solitary and immersed amongst strands of surrounding muscle cells. Only occasional synaptic impacts could be identified on the surface of neuronal bodies of these bipolar neurons. On the other hand, their dendritic varicosities were richly innervated. Due to their irregular shape, intimate association with muscular elements and their topographical superposition with occasional spindle-like structures, these nerve cells recall prospective sensory neurons involved in integration of mechanical and neural stimuli to the heart. (3) Small multipolar interneurons could be identified in the retronodal ganglion and within right and left bundle branches. The present description of morphological heterogeneity of intramural nerve cells agrees with recent morphological and functional classifications of autonomic neurons and supports the idea that, at the level of the atrioventricular junction, a self-governed neuronal network may be operating.

Morphology and histology of the digestive tract of Nautilus pompilius and Nautilus macromphalus (Cephalopoda, Tetrabranchiata)

This study presents histological and scanning electron microscopical findings on the structural differentiation, and the nervous and vascular supply of the digestive tracts of Nautilus pompilius and N. macromphalus, including the foregut, stomach, vestibulum, caecum, midgut and rectum. The stereoscopic reconstruction of the vestibulocaecal complex gives an idea how the digestive cycle between the stomach, vestibulum, caecum and proximal midgut could possibly proceed. All parts of the digestive tract are covered luminally by a columnar epithelium which contains numerous goblet cells. The epithelium is ciliated in the vestibulum, caecum, proximal midgut and the longitudinal groove of the rectum. On this lamina epithelialis mucosae borders the lamina propria mucosae, which consists of connective tissue and some muscle cells. In the stomach it is differentiated, forming a special bolster-like layer. The lamina propria mucosae is followed by the tunica muscularis, which consists of a stratum circulare and a stratum longitudinale in the foregut, vestibulum, caecum, midgut and rectum. In the stomach, midgut and rectum, the tunica adventitia, which consists of a thin layer of connective tissue, is located between the tunica muscularis and the cuboidal tunica serosa.

Solitary bone cyst in the odontoid process and body of the axis

A four-year-old boy presented with a solitary bone cyst in the odontoid process and body of the axis. Plain radiographs showed a radiolucent lesion with extreme thinning of the cortex and MRI demonstrated a high signal intensity in the interlesional matrix. The cystic component extended into the body of the axis through a defect in the epiphyseal plate. At operation, the cavity of the cyst was found to contain serosanguineous fluid, and histological examination showed that it was lined by a thin layer of connective tissue. The cyst may have originated from a defect in the epiphyseal plate.

Heat-producing organ of the swordfish (Xiphias gladius): A modified eye muscle.

In swordfish (Xiphias gladius), the dorsal rectus muscle of the eye (M. rectus dorsalis) is partly differentiated for heat production similar to brown adipocytes. Other parts of the dorsal rectus show a typical muscular structure. This modified muscle and its anatomical relationships to neighboring organs were investigated using macroscopic dissections, light and transmission electron microscopy, nuclear magnetic resonance tomography, and scanning electron microscopy of vascular corrosion casts. The ophthalmic artery off the efferent pseudobranchial artery supplies the dorsal rectus muscle. The ophthalmic artery branches in a brush-like manner as it enters the origin of the muscle. In this region, numerous arterioles and venules are arranged in parallel, suggesting a countercurrent heat exchange mechanism. Thermogenic cells, morphologically similar to brown adipocytes, surround small vascular branches in the middle of the muscle. Muscular cells also extend into this area. The vessels then divide into a tree-like pattern, forming an extensively capillarized area near the surface of the muscle at the basisphenoid bone. The basisphenoid is reduced to a thin connective tissue layer in this area, hence facilitating thermal transfer between the blood in the muscle and the brain base. The Tela lymph-adiposa surrounds the brain with large masses of fat. Additionally, voluminous masses of periocular fat provide thermal insulation lateral to the lateral rectus muscle of the eye. It is suggested that this system for raising the temperature of areas of the brain a few degrees above ambient temperature allows an optically oriented predator such as the swordfish to respond to optical input in cold water more efficiently. J. Morphol. 234:89-96, 1997. © 1997 Wiley-Liss, Inc.

Long-term in vivo degradation and bone reaction to various polylactides : 1. One-year results

Injection-moulded pins from poly( l-lactide), poly( l/dl-lactide) (95/5%) were implanted in the cortex of the tibiae of sheep. The bone-implant interface was evaluated to observe whether there is any bone resorption caused by the implants. The molecular weight and crystallinity changes upon implantation were also measured. There was no net bone loss around the implants or sterile cyst formation in any of the animals implanted with polylactides up to 1 year. The new bone formed around the poly( l-lactide) and poly( l/d-lactide) pins was separated from the implants with a thin layer of connective tissue. For the implants from poly( l/dl-lactide), there was direct apposition of bone on the polymeric material. At 1 year of implantation, the implants were not completely resorbed, although the molecular weight of polylactides was reduced from 40000–50000 to 500–3000. The crystallinity at 1 year was about 45% for poly( l/d-lactide) and poly( l/dl-lactide) and 65% for poly( l-lactide), respectively, indicating the presence in the degraded material of thermodynamically stable crystals.

Penile bulb and its relationship with the pelvic urethra and the penile urethra in the rat: Light and scanning electron microscopical observations

In male rats the urethral tract consists of the following parts: the pelvic urethra, the transitional urethra, the urethral diverticle, and the penile urethra. Perusal of the literature results in only some more general descriptions and a very few which go more into detail. None of the latter deals with all the compartments nor with the relationships between each other. Aim of this study is to give a detailed morphological study of all the urethral compartments and their relationships to provide a platform for further experimental investigations. From 40 adult male Wistar rats the urethral tract has been investigated by histology and scanning electron microscopy using intact tissue and casting techniques. Most striking is the existence of the sinusoids in the spongious tissues in the pelvic urethra into a system of two perpendicular layers of parallel sinusoids. In the spongious tissues of the penile corpus spongiosum the same organization can be found although less prominent. Smooth muscle cells are very unequally present along the urethral tract. In its pelvic part they do not form a continuous layer around the spongious tissue and compared to the distal part they appear proximally more abundant. In the bulbal part of the corpus spongiosum the smooth muscles form a massive sac around the spongious tissue. In the corpus spongiosum in the penile shaft they are absent. The smooth muscle cells are separated from the striated urethral muscle by a very thin layer of connective tissue, in the penile bulb a prominent tunica albuginea separates them from the striated penile muscles. In the spongious tissues of the pelvic urethra and the penile bulb large amounts of compound urethral glands are present. Their ducts open into the respective lumen. Helicine arteries are common in the pelvic urethra, especially in the glandular tissue. They are also normally present in the wing tips of the penile bulb. The transitional urethra, the urethral diverticle and surrounding spongious tissue are structurally closely related to the other parts, however their microscopical organization is intermediate between the pelvic part of the urethra and the corpus spongiosum. The highly ordered sinusoids in the spongious layers especially in the pelvic part together with a similar organization of the urethral muscle provide a possible basis for a peristaltic driving mechanism, suggesting these structures play a role in the high speed transport of sperms during ejaculation.

Histology and ultrastructure of the hepatopancreas of the tigerfish, Hydrocynus forskahlii.

Study of the histology and ultrastructure of the hepatopancreas of the tigerfish, Hydrocynus forskahlii shows that the liver parenchyma is divided into irregularly shaped lobules, separated by the exocrine pancreas and associated connective tissue. The hepatocytes are arranged in interconnecting cords or laminae, two to three cell layers in thickness. Sinusoids separate the laminae. The spherical to oval-shaped hepatocytes contain large, round, centrally situated nuclei with prominent nucleoli. The cytoplasm of the hepatocytes contains abundant rough and smooth endoplasmic reticulae, free polysomes, and mitochondria. Exocrine pancreatic tissue is scattered throughout the liver. This tissue is encapsulated by an endothelium resting on a thin layer of connective tissue and is separated from the liver parenchyma by a sinusoid. The nuclei of the exocrine pancreas cells are spherical, basally situated within the cells, and contain dark nucleoli. Vesicular rough endoplasmic reticulae and secretory granules lie in the apical regions of the exocrine pancreas cells. © 1996 Wiley-Liss, Inc.