eMedicine Specialties > Orthopedic Surgery > Neoplasms

Histology of Bone

Yi Jun Yang, MD, PhD, Clinical Assistant Professor, Department of Pathology, State University of New York Upstate; Consulting Staff, Department of Pathology, Oneida Health Care Center
Timothy A Damron, MD, David G Murray Endowed Professor, Department of Orthopedic Surgery, Professor, Orthopedic Oncology and Adult Reconstruction, Vice Chair, Department of Orthopedics, State University of New York Upstate Medical University at Syracuse

Updated: Jan 28, 2008

Introduction

Basic functions of bone

Bone is the basic unit of the human skeletal system and provides the framework for and bears the weight of the body, protects the vital organs, supports mechanical movement, hosts hematopoietic cells, and maintains iron homeostasis.^{1,2,3,4,5,6,7,8}

For excellent patient education resources, visit eMedicine's Bone, Joint, and Muscle Center, Osteoporosis and Bone Health Center, and Breaks, Fractures, and Dislocations Center. Also, see eMedicine's patient education articles Osteoporosis, Fall Prevention and Osteoporosis, and Vitamin D: Vital Role in Your Health.

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Classification of bone

Bones can be classified based on their position, shape, size, and structure.

Based on location, bones can be classified as follows:

• Axial skeleton – Bones of the skull, vertebral column, sternum, and ribs
• Appendicular skeleton – Bones of the pectoral girdle, pelvis girdle, and limbs
  • Acral skeleton – Part of the appendicular skeleton, including bones of the hands and feet

Based on shape, bones can be classified as follows:

• Flat bone – Bones of the skull, sternum, pelvis, and ribs
• Tubular bone –
  • Long tubular bone, including bones of the limbs
  • Short tubular bone, including bones of the hands and feet, such as the phalanges, metacarpals, and metatarsals
• Irregular bone – Bones of the face and vertebral column
• Sesamoid bone – Bones that develop in specific tendons, the largest example of which is the patella
• Accessory bone or supernumerary bone - Extra bones that develop in additional ossification centers or bones that failed to fuse with the main parts during development (Accessory bones are common in the foot and may be mistaken for bone chips or fractures.)

Based on size, bones can be classified as follows:

• Long bone – Tubular in shape, with a hollow shaft and 2 ends, including bones of the limbs
• Short bone – Cuboidal in shape, located only in the foot (tarsal bones) and wrist (carpal bones)

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Gross structures of bone

The gross structure of a long bone can be divided into several regions.

Epiphysis

In the long bones, the epiphysis is the region between the growth plate or growth plate scar and the expanded end of bone, covered by articular cartilage. An epiphysis in a skeletally mature person consists of abundant trabecular bone and a thin shell of cortical bone (see Image 1). Although an epiphysis is present at each end of the long limb bones, it is found at only one end of the metacarpals (proximal first and distal second through the fifth metacarpals), metatarsals (proximal first and distal second through fifth metatarsals), phalanges (proximal ends), clavicles, and ribs.

The epiphysis is the location of secondary ossification centers during development. The structure of the epiphysis is more complex in bones that are fused from more than one part during development. Examples include the proximal and distal ends of the humerus, femur, and vertebrae. For instance, the proximal end of the humerus is developed from 3 separate ossification centers, which later coalesce to form a single epiphyseal mass. In the proximal humeral epiphysis, one of the centers forms the articular surface, and the other 2 become the greater and lesser tuberosities. Carpal bones, tarsal bones, and the patella are also called epiphysioid bones and are developmentally equivalent to the epiphyses of the long bones.

Knowledge of the location of the epiphysis and its equivalents in various bones aids clinicians in the recognition of the origin of bone lesions and further facilitates the diagnostic considerations, as some bone tumors such as chondroblastoma have a strong predilection for the epiphysis or epiphysioid bones.

Metaphysis

The metaphysis is the junctional region between the growth plate (see Image 2) and the diaphysis. The metaphysis contains abundant trabecular bone, but the cortical bone thins here relative to the diaphysis. This region is a common site for many primary bone tumors and similar lesions. The relative predilection of osteosarcoma for the metaphyseal region of long bones in children has been attributed to the rapid bone turnover due to extensive bone remodeling during growth spurts (see Growth, Modeling, and Remodeling of Bone, below).

Osteosarcoma is a malignant primary bone tumor that is characterized by neoplastic osteoblasts that produce osteoid. Because of increased osteoblastic activity, the serum level of alkaline phosphatase is often significantly increased in this disease; however, acid phosphatase is synthesized by osteoclasts and will not be significantly increased in this disease, although scattered osteoclasts can also be present. The Codman triangle is a pattern of periosteal reaction that is often associated with osteosarcoma, although this pattern may also be seen with other aggressive processes, including osteomyelitis.

Diaphysis

The diaphysis is the shaft of long bones and is located in the region between metaphyses, composed mainly of compact cortical bone. The medullary canal contains marrow and a small amount of trabecular bone.

Physis (epiphyseal plate, growth plate)

The physis is the region that separates the epiphysis from the metaphysis. It is the zone of endochondral ossification in an actively growing bone or the epiphyseal scar in a fully grown bone.

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Blood supply of bone

Bone has a rich vascular supply, receiving 10-20% of the cardiac output. The blood supply varies with different types of bones, but blood vessels are especially rich in areas that contain red bone marrow.

Long bones

• Diaphyseal nutrient artery: This is the most important supply of arterial blood to a long bone. One or 2 principal diaphyseal nutrient arteries first pass obliquely through the cortical bone. These arteries then divide into ascending and descending branches and supply the inner two thirds of the cortex and medullary cavity.
• Metaphyseal and epiphyseal arteries: Numerous metaphyseal and epiphyseal arteries supply the ends of bones. These blood vessels mainly arise from the arteries that supply the adjacent joint, anastomose with the diaphyseal capillaries, and terminate in bone marrow, cortical bone, trabecular bone, and articular cartilage. In growing bones, these arteries are separated by the epiphyseal cartilaginous plates.
• Periosteal arterioles: Several of these vessels supply the outer layers of cortical bone.

Large irregular bones, short bones, and flat bones

These bones receive a superficial blood supply from the periosteum, as well as frequently from large nutrient arteries that penetrate directly into the medullary bone. The 2 systems anastomose freely.

Venous and lymphatic drainage of bone

Blood is drained from bone through veins that accompany the arteries and frequently leaves through foramina near the articular ends of the bones. Lymph vessels are abundant in the periosteum.

Nerve supply of bone

Nerves are most rich in the articular extremities of the long bones, vertebrae, and larger flat bones. Many nerve fibers accompany the blood vessels to the interior of the bones and to the perivascular spaces of the haversian canals.

The periosteal nerves are sensory nerves, some of which are pain fibers. Therefore, the periosteum is especially sensitive to tearing or tension.

Accompanying the arteries inside the bones are vasomotor nerves, which control vascular constriction and dilation.

Bone Tissue Types and Structure

Types of bone tissue

• Compact bone (dense bone, cortical bone): Compact bone is ivorylike and dense in texture without cavities. It is the shell of many bones and surrounds the trabecular bone in the center. Compact bone consists mainly of haversian systems or secondary osteons.
• Sponge bone (trabecular bone, cancellous bone): Sponge bone is so named because it is spongelike with numerous cavities. It is located within the medullary cavity and consists of extensively connected bony trabeculae (see Images 3-4) that are oriented along the lines of stress.
  • In contrast to compact bone, complete osteons are usually absent in sponge bone due to the thinness of the trabeculae.¹⁰ Sponge bone is also more metabolically active than compact bone because of its much larger surface area for remodeling.

Based on matrix arrangement, bone tissue can be classified as follows:

• Lamellar bone (secondary bone tissue): Lamellar bone is mature bone with collagen fibers that are arranged in lamellae. In contrast to sponge bone, in which lamellae are arranged parallel to each other, in compact bone, the lamellae are concentrically organized around a vascular canal, termed a haversian canal.
• Woven bone (primary bone tissue): Woven bone (see Image 5) is immature bone, in which collagen fibers are arranged in irregular random arrays and contain smaller amounts of mineral substance and a higher proportion of osteocytes than lamellar bone. Woven bone is temporary and is eventually converted to lamellar bone; this type of bone is also pathologic tissue in adults, except in a few places, such as areas near the sutures of the flat bones of the skull, tooth sockets (see Image 6), and the insertion site of some tendons (see Image 7).

Based on maturity, bone tissue can be classified as follows:

• Immature bone (primary bone tissue): Immature bone is woven bone.
• Mature bone (secondary bone tissue) (see Image 8): Mature bone is characteristically lamellar bone. Almost all bones in adults are lamellar bones.

Based on developmental origin, bones can be classified as follows:

• Intramembranous bone (mesenchymal bone): Intramembranous bone develops from direct transformation of condensed mesenchyme. Flat bones are formed in this way.
• Intracartilaginous bone (cartilage bone, endochondral bone): Intracartilaginous bone forms by replacing a reformed cartilage model. Long bones are formed in this way.

Microscopic structure of bone

Bone cells

• Osteoblasts
  • Osteoblasts (see Image 9) are located on the surface of bone or osteoid, and they are responsible for synthesizing the organic components of the bone matrix, including type I collagen, proteoglycans, and glycoproteins. Osteoblasts also synthesize the enzyme alkaline phosphatase, which is needed locally for the mineralization of osteoid.¹¹
  • Although an active osteoblast (see Image 10) has a cuboidal or columnar shape with an eccentrically located nucleus and a perinuclear cytoplasmic halo, an inactive osteoblast has a flattened shape with low alkaline phosphatase activity. Osteoblasts contact their neighboring osteoblasts cytoplasmically.
  • Osteoblasts do not divide. They give rise to osteocytes, remain as osteoblasts, or return to the state of osteoprogenitor cells from which they derived.
• Osteocytes
  • An osteoblast becomes an osteocyte when the cell is encased by osteoid matrix that it synthesizes itself. Lacunae and canaliculi form around the osteocyte and its cytoplasmic processes, respectively.¹² Thus, an osteocyte lies in its own lacuna and contacts its neighboring osteocytes cytoplasmically through canaliculi (see Image 11).
  • The processes of adjacent cells make contact via gap junctions, maintaining the vitality of osteocytes by passing nutrients and metabolites between blood vessels and distant osteocytes, regulating ion homeostasis, and transmitting electrical signals in bone.¹³
  • Although osteocytes have reduced synthetic activity and are not capable of mitotic division, they are actively involved with the maintenance of the bony matrix. Some of the osteocytes die during remodeling, but most probably return to the state of osteoprogenitor cells or persist as osteocytes for a long time.
• Osteoclasts^{2,14,15,16,17}
  • Osteoclasts (see Image 12) are probably derived from a monocytic-macrophage system and are responsible for bone resorption. They are multinucleated cells with fine, fingerlike cytoplasmic processes and are rich in lysosomes that contain tartrate-resistant acid phosphatase (TRAP).
  • Osteoclasts lie in resorption craters known as Howship lacunae (see Image 13) on bone surfaces or in deep resorption cavities called cutting cones. These bone cells can only resorb mineralized bone matrix.
  • Cells that express the full morphologic and functional properties of mature osteoclasts are known to be restricted to the surfaces of bones.
    • Osteoclast transmigration on the bone surface has been assumed to be for the purpose of bone resorption. A study by Saltel et al appears to have demonstrated a new property of mature osteoclasts: transmigration through bone tissues of various cell types.¹⁸  The authors' results may have implications for therapeutic strategies for bone diseases with an imbalance in bone remodeling that is caused by excessive osteoclast resorption.
    • Research is also under way to investigate whether "components of the bone matrix and specific cell surface receptors on osteoclasts and their precursors play an essential role in determining the genetic profile and functional properties of fully differentiated resorbing osteoclasts."¹⁹
  • Osteoclasts or their committed precursors do not have receptors for parathyroid hormone. The hormonal signal is mediated by osteoblasts.²⁰ However, osteoclasts do have receptors for calcitonin.
  • When in an active state, osteoclasts create an effect that always predominates over that of osteoblasts because osteoclasts are three times more efficient at bone resorption than osteoblasts are at bone deposition. In balance, osteoclasts have a much shorter life span than osteoblasts.
  • Osteoclasts are rarely seen in routine histologic sections of normal bone. An increased number of osteoclasts is characteristic of diseases with increased bone turnover.

Bone matrix

Bone matrix consists of organic and inorganic components. The association of organic and inorganic substances gives bone its hardness and resistance. The organic component is composed of collagen fibers with predominately type I collagen (95%) and amorphous material, including glycosaminoglycans that are associated with proteins.^21,22 Osteoid is uncalcified organic matrix. Inorganic matter represents about 50% of the dry weight of bone matrix, composed of abundant calcium and phosphorus, as well as smaller amounts of bicarbonate, citrate, magnesium, potassium, and sodium. Calcium forms hydroxyapatite crystals with phosphorus but is also present in an amorphous form.

During bone remodeling, osteoblasts deposit a layer of osteoid seam (approximately 10 µm thick) on the surface of preexisting bone, which then begins to mineralize in approximately 20 days.²³ This interval is known as the mineralization lag time.

In the histology of normal bone, as a result of the normal remodeling process, up to 20% of the bone surface may be covered by osteoid (usually 10 µm thick). An increased amount of osteoid is seen in pathologic conditions in which the remodeling rate is accelerated or in which the mineralization lag time is increased.

Microscopic architecture of bone

• Haversian system (secondary osteon)
  • The primary structural unit of compact bone is the haversian system. Each haversian system is a long, often bifurcated, cylinder that is parallel to the long axis of bone, formed by successive deposition of 4-20 (average 6) concentric layers of lamellae.
  • Collagen fibers are parallel to each other within each lamella, but they are oriented perpendicularly to the fibers in the neighboring lamellae.²⁴ Such an arrangement can be highlighted as alternating bright and dark layers in polarized microscopy (see Image 8).
  • Lamellar deposition starts from the periphery, so that younger lamellae are closer to the center of the system, and the younger systems have larger canals. Between the lamellae are lacunae that contain the cell bodies and canaliculi that hold the cytoplasmic processes of osteocytes.
  • In the center of each haversian system is a haversian canal, which is lined by endosteum and contains a neurovascular bundle and loose connective tissue.
    • The haversian canals connect with each other by transverse or oblique Volkmann canals that communicate with the marrow cavity and the periosteum to provide channels for the neurovascular system. Volkmann canals are not surrounded by concentric lamellae; rather, they perforate the lamellae.
• Interstitial lamellae
  • Interstitial lamellae are incomplete or fragmented osteons that are located between the secondary osteons. They represent the remnant osteons left from partial resorption of old osteons during bone remodeling.
  • The mixture of interstitial lamellae and complete osteons produces a mosaic pattern. Thus, the age of the bone can be deduced from the proportion of interstitial lamellae and intact osteons. Younger bone has more complete osteons and less interstitial lamellae in between the osteons.
    • The age of bone also affects osteoclast activity in bone resorption. In a study by Henriksen et al, the authors demonstrated that osteoclasts preferentially differentiate and resorb bone on aged bone than they do on young bone.¹⁴
• Circumferential lamellae
  • Circumferential lamellae are circular lamellae that line the external surface of the cortex adjacent to the periosteum and line the inner surface of the cortex next to the endosteum.
  • There are more outer than inner circumferential lamellae.

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Histogenesis of Bone

Bone tissue arises by intramembranous ossification or by endochondral ossification.^6,25 In either case, the original or model tissue is gradually destroyed and replaced with bone tissue. Bone forms only by appositional deposition of matrix on the surface of a preformed tissue. Woven bone is initially formed and is then later converted to lamellar bone by subsequent remodeling.

Intramembranous ossification

Although intramembranous ossification (see Image 14) is the source of flat bones, this process also contributes to the growth of short bones and thickening of long bones. Interstitial membranous ossification takes place within a condensation of mesenchymal tissue. The process begins when multiple groups of cells differentiate into osteoblasts in a primary ossification center.

Osteoid is synthesized and then mineralized surrounding the osteoblasts, which then become osteocytes. When these ossification centers fuse, a loose trabecular structure known as primary spongiosa is formed. Subsequently, blood vessels grow into the connective tissue between the trabeculae. Bone marrow stem cells from the circulating blood then give rise to hematopoietic cells.

Growth and fusion of several ossification centers (see Image 15) eventually replace the original mesenchymal tissue. In flat bones, compact bone is formed at both the internal and external surfaces due to a marked predominance of bone deposition over bone resorption, whereas a spongy pattern remains in the central portion. The endosteum and periosteum are formed from layers of connective tissue that are not undergoing ossification.

Endochondral ossification can be divided into 2 phases. In the first phase, chondrocytes of the model are hypertrophic and degenerated, and then the intervening chondroid matrix is calcified. In the second phase, osteogenic buds, composed of osteoprogenitor cells and blood capillaries, invade the spaces left by the degenerating chondrocytes.

Osteoblasts arise from osteoprogenitor cells and lay down a layer of rapidly mineralized osteoid on the surface of calcified cartilage. The complex structure of calcified cartilage with overlying newly bone thus formed is known as the primary spongiosa, which is later remodeled to become lamellar bone (secondary spongiosa). Calcified cartilage remnants are resorbed by chondroclasts, which are structurally and functionally equivalent to osteoclasts, except that chondroclasts work on cartilage rather than bone. Thus, the cartilage model is gradually replaced by bone and marrow cavities.

Long bones are formed from cartilaginous models. The primary ossification center is initiated by intramembranous ossification that is produced by the deep portions of the perichondrium that surround the diaphysis. A bone collar is thus formed, blocking the nutrient diffusion and leading to the degeneration of internal chondrocytes. The perichondrium then becomes the periosteum, from which the osteogenic bud arises and penetrates the calcified cartilage matrix through passages that are created in the bone collar by osteoclasts.

The primary ossification center expands longitudinally and is associated with the growth of the periosteal bone collar. Osteoclasts are activated at the beginning of the process, resorb the bone at the center, and hence create the marrow cavity. At a later stage of bone development, a secondary ossification center arises at the center of each epiphysis. Unlike primary ossification, which expands in a longitudinal fashion, the secondary ossification center grows in a radial fashion. Furthermore, a bone collar is not formed in the area of articular cartilage due to the absence of perichondrium in this area. Thus, the epiphysis of the chondroid model is replaced by bone tissue, except the articular cartilage and the epiphyseal cartilage.

Epiphyseal cartilage is located between the epiphysis and the metaphysis and is responsible for the longitudinal growth of bone. It can be divided into 5 zones, starting from the epiphyseal side of cartilage, as follows:

• Resting zone – This zone consists of small chondrocytes.
• Proliferative zone – The proliferative zone consists of rapidly dividing chondrocytes in columns that are parallel to the long axis of the bone, resulting in interstitial growth of cartilage. The chondroid matrix is laid down, and mitotic figures may be detected.
• Hypertrophic zone – This zone consists of large chondrocytes that contain abundant cytoplasmic glycogen. In the hypertrophic zone, chondrocytes mature and degenerate, with associated chondroid matrix resorption.
• Calcified cartilage zone (zone of provisional calcification) – This zone is where chondrocytes die. Chondrocyte death is followed by blood vessel invasion and bone deposition on the calcified cartilage.
• Ossification zone – The ossification zone is where primary spongiosa forms by rapidly mineralized osteoid that is laid down on the calcified cartilage septa (see Image 17).

During growth, the epiphyseal plate normally does not change in thickness because the rates of proliferation and destruction are approximately equal. It is simply replaced away from the middle of the diaphysis, resulting in longitudinal growth of the bone. When the epiphyseal plate closes, between ages 16 and 20 years, the longitudinal growth of bones becomes impossible, although widening may still occur through appositional growth.

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Growth, Modeling, and Remodeling of Bone

Similar to development, bone also grows by either endochondral ossification or intramembranous ossification. Whereas endochondral ossification of the epiphyseal plate is responsible for longitudinal growth of the long bones, periosteal deposition contributes to both the length and thickness of long bones, as well as the overall growth of flat bones.

Endosteal bone deposition contributes to the growth of trabecular bone and the endosteal cortex, including the haversian system. The ongoing process that alters the size and shape of bone by partial resorption of preformed bone tissue and simultaneous deposition of new bone is modeling and remodeling.^{1,2,3,4,5,6,7,8}  This process begins when a new bone is formed.

Modeling is a process in which bone is sculpted during growth to ultimately achieve its proper shape. Modeling is responsible for the circumferential growth of the bone and expansion of the marrow cavity, modification of the metaphyseal funnel of long bones, and enlargement of the cranial vault curvature.

Remodeling is a continuous process throughout life, in which damaged bone is repaired, ion homeostasis is maintained, and bone is reinforced for increased stress. In adults, the remodeling rate varies in different types of bones. Trabecular bone is remodeled at a higher rate (25% per year) than that of cortical bone (3% per year) in a healthy adult.

Resorption and deposition are normally balanced, and bone density is maintained. A lytic lesion results when resorptive activity exceeds deposition activity in a pathologic state. The cement line (reversal line) is evidence of previous remodeling activity and is formed by filling of new bone in a previously resorbed cavity (see Image 18). The cement line is strongly basophilic due to the high content of inorganic matrix and is normally found in the haversian and interstitial systems of adult bone. The relative amount of cement lines corresponds to the amount of remodeling that has occurred. An entire remodeling cycle requires approximately 6 months. Although a cement line that results from normal remodeling is relatively long and straight, an indented or mosaic pattern indicates a pathologically accelerated remodeling process.

Supportive and Connective Structures of Bone

Joints²⁵

Bones are connected to each other by joints to form the skeletal system, as follows:

• Synostosis joint – Nonmovable joint; the bones are connected by bone tissue or dense connective tissue (eg, skull bones are joined by bone tissue in adults but by dense connective tissue in children)
• Synchondrosis joint – Joint with limited movement; the bones are connected by hyaline cartilage (eg, the costochondral joints between ribs and sternum)
• Syndesmosis joint – Joint with limited movement; the bones are joined by an interosseous membrane (eg, tibiofibular and radioulnar articulations)
• Diarthrosis joint – Joint that permits great mobility (eg, knee and hip joints) and consists of a capsule, an articular cavity that contains synovial fluid rich in hyaluronic acid, and articular cartilage that covers the epiphyses of the 2 involved adjoining bones
• Symphysis joint – Joint with limited movement (eg, the joint between vertebral bodies [intervertebral discs], the joint between pubic bones [pubic symphysis]), in which bones are covered by hyaline cartilage on the articulating surface and are united by fibrous tissue and/or fibrocartilage
• Gomphosis joint – Nonmovable joint, in which fibrous tissue anchors a tooth and the bone in the alveolus

Periosteum

The periosteum is composed of an inner cambium layer that is immediately adjacent to the bone surface and an outer dense fibrous layer. The cambium layer consists of osteoprogenitor cells, which are flat and spindle shaped and are capable of differentiating into osteoblasts and forming bones in response to various stimulations (see Image 19). The collagen fibers in the outer layer are contiguous with the joint capsule, ligament, and tendons. The periosteum is thick and loosely attached to the cortex in children, but it is thinner and more adherent in adults. The periosteum completely covers a bone, except in the region of the articular cartilage and at sites of muscle attachments. It is somewhat anchored to the cortex by Sharpey fibers that penetrate into the bone.

The periosteum carries a dense network of blood, lymphatic vessels, and predominantly sensory nerves for maintenance of the bone structure. Different patterns of periosteal stimulation result in different patterns of periosteal bone formation. Continual insult results in streams of periosteal bone that are perpendicular to the bone surface, resulting in a hair-on-end appearance on radiographs. Intermittent periosteal stimulation results in multiple partially separated streams of periosteal bone that are parallel to the bone surface, giving an onionskin appearance on radiographs.

Multimedia

Media file 1: Cortical bone is composed of haversian systems (osteons). Each osteon has a central haversian canal and peripheral concentric layers of lamellae.

Media file 2: Growth plate.

Media file 3: Trabecular bone and the surrounding hematopoietic cells, as well as adipose tissue in medullary cavity.

Media file 4: Mature trabecular bone exhibits lamellae and osteocytes between the lamellae. Inactive osteocytes are also present on the bone surface with a flattened shape.

Media file 5: Woven bone under a polarized microscope; collagen fibers are arranged in disorganized arrays.

Media file 6: Tooth socket in adults.

Media file 7: Tendon insertion site in adults.

Media file 8: Osteon of mature bone viewed under a polarized microscope; lamellae are shown as alternating dark and bright layers due to the perpendicular orientation of the collagen fibers in the neighboring lamellae.

Media file 9: Osteoblasts in cytologic preparation (Diff-Quik stain). Each active osteoblast has eccentrically located nuclei with a conspicuous nucleus and a perinuclear halo, resembling a plasma cell. However, the osteoblast does not exhibit the clock-face or wheel-like chromatin pattern that is seen in a plasma cell.

Media file 10: Active osteoblasts depositing osteoid on the surface of a woven bone trabecula. Osteoblasts are columnar or cuboidal shaped, with eccentric nuclei and perinuclear halo. These cells also have polarity, with the cytoplasm toward the bone but the nuclei at the end away from the bone.

Media file 11: Osteocytes are present in lacunae; their cytoplasmic processes contact each other through the canaliculi.

Media file 12: Osteoclast in a cytologic preparation (Papanicolaou stain). This image shows multiple nuclei and cytoplasmic processes.

Media file 13: Remodeling of bone. Multiple osteoclasts are sitting in the Howship lacunae, resorbing one side of a bony trabecula, while osteoblasts are depositing new bone on the other side.

Media file 14: Intramembranous ossification. Woven bone arises directly from the surrounding mesenchymal tissue.

Media file 15: Primary calcification center of fetal bone.

Media file 16: Endochondral ossification in a primary ossification center of a fetal chondral model. The chondrocytes are hypertrophic. Early calcification starts in the matrix between the chondrocytes. The surface of the chondral model is covered by perichondrium, which later becomes the periosteum.

Media file 17: Primary spongiosa in the ossification zone of growth plate. The osteoid is deposited at the periphery of calcified cartilage.

Media file 18: The cement line is evidence of a previous remodeling process.

Media file 19: Periosteal bone formation on the surface of cortical bone. New bone is deposited by osteoblasts derived from progenitor cells in the cambium layer of the periosteum.

Media file 20: The articular cartilage can be divided into 3 zones. The calcified zone is separated from the upper zone by a calcified line termed the tidemark. Duplication of the tidemark can be seen with aging, when the calcified cartilage is gradually replaced by endochondral bone formation. Consequently, the calcified zone pushes into the upper zone.

Media file 21: Synovial membrane is partly a smooth connective tissue and partly a villous fibrovascular connective tissue that is lined by a single layer of synovial epithelium.

Media file 22: The meniscus is composed of fibrocartilage.

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Keywords

osteoblast, osteocyte, osteoclast, haversian system/canal, lamellae, ossification, endosteum, synovium, cartilage, joints, bone growth, bone development

Contributor Information and Disclosures

Author

Yi Jun Yang, MD, PhD, Clinical Assistant Professor, Department of Pathology, State University of New York Upstate; Consulting Staff, Department of Pathology, Oneida Health Care Center
Yi Jun Yang, MD, PhD is a member of the following medical societies: American Society of Clinical Pathologists, American Society of Cytopathology, College of American Pathologists, and International Academy of Pathology
Disclosure: Nothing to disclose.

Coauthor(s)

Timothy A Damron, MD, David G Murray Endowed Professor, Department of Orthopedic Surgery, Professor, Orthopedic Oncology and Adult Reconstruction, Vice Chair, Department of Orthopedics, State University of New York Upstate Medical University at Syracuse
Timothy A Damron, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American College of Surgeons, American Medical Association, Children's Oncology Group, Connective Tissue Oncology Society, Musculoskeletal Tumor Society, Orthopaedic Research Society, and Society for Experimental Biology and Medicine
Disclosure: Nothing to disclose.

Medical Editor

Timothy A Damron, MD, David G Murray Endowed Professor, Department of Orthopedic Surgery, Professor, Orthopedic Oncology and Adult Reconstruction, Vice Chair, Department of Orthopedics, State University of New York Upstate Medical University at Syracuse
Timothy A Damron, MD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American College of Surgeons, American Medical Association, Children's Oncology Group, Connective Tissue Oncology Society, Musculoskeletal Tumor Society, Orthopaedic Research Society, and Society for Experimental Biology and Medicine
Disclosure: Nothing to disclose.

Pharmacy Editor

Francisco Talavera, PharmD, PhD, Senior Pharmacy Editor, eMedicine
Disclosure: Nothing to disclose.

Managing Editor

Sean P Scully, MD, PhD, Professor, Department of Orthopedics, University of Miami
Sean P Scully, MD, PhD is a member of the following medical societies: American Academy of Orthopaedic Surgeons, International Society on Thrombosis and Haemostasis, and Society of Surgical Oncology
Disclosure: Nothing to disclose.

CME Editor

Dinesh Patel, MD, FACS, Associate Clinical Professor of Orthopedic Surgery, Harvard Medical School; Chief of Arthroscopic Surgery, Department of Orthopedic Surgery, Massachusetts General Hospital
Dinesh Patel, MD, FACS is a member of the following medical societies: American Academy of Orthopaedic Surgeons, American Association of Physicians of Indian Origin, American College of International Physicians, and American College of Surgeons
Disclosure: Nothing to disclose.

Chief Editor

Harris Gellman, MD, Consulting Surgeon, Broward Hand Center, Voluntary Clinical Professor of Orthopedic Surgery and Plastic Surgery, Departments of Orthopedic Surgery and Surgery, University of Miami School of Medicine
Harris Gellman, MD is a member of the following medical societies: American Academy of Medical Acupuncture, American Academy of Orthopaedic Surgeons, American Orthopaedic Association, American Society for Surgery of the Hand, and Arkansas Medical Society
Disclosure: Nothing to disclose.

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