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More Ch. 6 6.5 – 6.10

More Ch. 6 6.5 – 6.10. Bone Growth, Composition and Conditions . Ossification . Skeleton begins to form in embryo at 6 week During all future development bone undergoes increases in size and ossification Ossification = bone formation Calcification = deposition of calcium

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More Ch. 6 6.5 – 6.10

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  1. More Ch. 66.5 – 6.10 Bone Growth, Composition and Conditions

  2. Ossification • Skeleton begins to form in embryo at 6 week • During all future development bone undergoes increases in size and ossification • Ossification = bone formation • Calcification = deposition of calcium • Endochondral ossification = bone replaces cartilage that was already presesnt • Intramembranous ossification = bone develops directly from connective tissue • Bone growth continues through adolescence, and on average until about age 25 • Toes “done” by age 11; pelvis and wrists may still be growing at 25. Lots of growth happens in relation to puberty hormones

  3. Endochondryal Ossification • Chondros = cartilage • Endo = inside • Most bones start as hyaline cartilage and are “models of adult bone” size and shape • Cartilage gradually replaced by bone • Time line: • 6 weeks proximal end of limb bone present but as hyaline cartilage • New cartilage on outer surface • Cells at center enlarge, blood vessels grow • Primary ossification starts and spread toward ends • Increases in length and in diameter • Centers of epiphyses calcify and become spongy bone • Cap of cartilage remains at articulation • Region of cartilage between epiphysis and diaphysis = lengthening bone

  4. Figure 6-10 Endochondral Ossification (Step 1-7) As the cartilage enlarges, chondrocytes near the center of the shaft increase greatly in size. The matrix is reduced to a series of small struts that soon begin to calcify. The enlarged chondrocytes then die and disintegrate, leaving cavities within the cartilage. Blood vessels grow around the edges of the cartilage, and the cells of the perichondrium convert to osteoblasts. The shaft of the cartilage then becomes ensheathed in a superficial layer of bone. Blood vessels penetrate the cartilage and invade the central region. Fibroblasts migrating with the blood vessels differentiate into osteoblasts and begin producing spongy bone at a primary ossification center. Bone formation then spreads along the shaft toward both ends. Remodeling occurs as growth continues, creating a medullary cavity. The osseous tissue of the shaft becomes thicker, and the cartilage near each epiphysis is replaced by shafts of bone. Further growth involves increases in length and diameter. Enlarging chondrocytes within calcifying matrix Epiphysis Medullary cavity Medullary cavity Blood vessel Primary ossification center Superficial bone Diaphysis Spongy bone Metaphysis Bone formation Hyaline cartilage Capillaries and osteoblasts migrate into the epiphyses, creating secondary ossification centers. Soon the epiphyses are filled with spongy bone. An articular cartilage remains exposed to the joint cavity; over time it will be reduced to a thin superficial layer. At each metaphysis, an epiphyseal cartilage separates the epiphysis from the diaphysis. This light micrograph shows the ossifying surface of an epiphyseal cartilage. The pink material is osteoid, deposited by osteoblasts in the medullary cavity. On the shaft side of the epiphyseal cartilage, osteoblasts are continuously invading the cartilage and replacing it with bone. On the epiphyseal side, new cartilage is continuously being added. The osteoblasts are therefore moving toward the epiphysis, which is being pushed away by the expansion of the epiphyseal cartilage. The osteoblasts won’t catch up to the epiphysis, as long as both the osteoblasts and the epiphysis “run away” from the primary ossification center at the same rate. Meanwhile, the bone grows longer and longer. Hyaline cartilage Epiphysis Articular cartilage Cartilage cells undergoing division and secreting additional cartilage matrix Metaphysis Epiphyseal cartilage matrix Spongy bone Periosteum Compact bone Epiphyseal cartilage Diaphysis LM  250 Secondary ossification center Medullary cavity Osteoblasts Osteoid

  5. Figure 6-10 Endochondral Ossification (Step 1-4) As the cartilage enlarges, chondrocytes near the center of the shaft increase greatly in size. The matrix is reduced to a series of small struts that soon begin to calcify. The enlarged chondrocytes then die and disintegrate, leaving cavities within the cartilage. Blood vessels grow around the edges of the cartilage, and the cells of the perichondrium convert to osteoblasts. The shaft of the cartilage then becomes ensheathed in a superficial layer of bone. Blood vessels penetrate the cartilage and invade the central region. Fibroblasts migrating with the blood vessels differentiate into osteoblasts and begin producing spongy bone at a primary ossification center. Bone formation then spreads along the shaft toward both ends. Remodeling occurs as growth continues, creating a medullary cavity. The osseous tissue of the shaft becomes thicker, and the cartilage near each epiphysis is replaced by shafts of bone. Further growth involves increases in length and diameter. Enlarging chondrocytes within calcifying matrix Epiphysis Medullary cavity Medullary cavity Blood vessel Primary ossification center Superficial bone Diaphysis Spongy bone Metaphysis Bone formation Hyaline cartilage

  6. Figure 6-10 Endochondral Ossification (Steps 5-7) This light micrograph shows the ossifying surface of an epiphyseal cartilage. The pink material is osteoid, deposited by osteoblasts in the medullary cavity. On the shaft side of the epiphyseal cartilage, osteoblasts are continuously invading the cartilage and replacing it with bone. On the epiphyseal side, new cartilage is continuously being added. The osteoblasts are therefore moving toward the epiphysis, which is being pushed away by the expansion of the epiphyseal cartilage. The osteoblasts won’t catch up to the epiphysis, as long as both the osteoblasts and the epiphysis “run away” from the primary ossification center at the same rate. Meanwhile, the bone grows longer and longer. Capillaries and osteoblasts migrate into the epiphyses, creating secondary ossification centers. Soon the epiphyses are filled with spongy bone. An articular cartilage remains exposed to the joint cavity; over time it will be reduced to a thin superficial layer. At each metaphysis, an epiphyseal cartilage separates the epiphysis from the diaphysis. Hyaline cartilage Epiphysis Articular cartilage Metaphysis Cartilage cells undergoing division and secreting additional cartilage matrix Epiphyseal cartilage matrix Spongy bone Periosteum Compact bone Epiphyseal cartilage Diaphysis LM  250 Secondary ossification center Osteoid Osteoblasts Medullary cavity

  7. APPOSITIONAL GROWTH = Superficial layers of bone forms early in endochondral ossification New growth in the bones diameter results in layers – New lamella added in concentric rings around outside while inner layers are recycled An x-ray of growing epiphyseal cartilages (arrows) Epiphyseal lines in an adult (arrows)

  8. Intramembranous Ossification • Osteoblasts differentiate • Fibrous connective tissue ( mesenchymal cells) • Matrix is created • Crystallization of calcium salts • Very active process requiring lots of nutrients • Osteoblasts ossification  spicules form • Initially only spongy bone • Remodeling can lead to compact bone • Creates dermal bones • Flat bones of skull, mandible (lower jaw), and clavicle (collar bone)

  9. Blood and nerve supply to bones • Bone maintenance and grow require blood supply • Osseous tissue is highly vascular • Nutrient artery and vein: supply diaphysis, usually only one of each ( femur has more) • Enter through foramina – branch into smaller canals • Metaphyseal vessels – supply blood to cartilage that is or will be replaced by bone • Periosteal vessels – blood to periosteum and superficial osteons – branch during ossification • All are very interconnected • Lymph – connect blood and lymph through osteons • Nerves – travel along nutrient artery ( injuries to bones are very painful)

  10. Remodeling • Bone matrix constantly being recycled and renewed • Used for both maintenance and changes to bone shape and structure • Youth – recycle about 1/5 of calcium salts per year; more likely in areas of spongy bone • Heavy metals are dangerous because they can be incorporated into bone – stay in circulatory system for many years. (Chernobyl Nuclear reactor leak; 1986 Ukraine, only other level 7 leak is Fukushuma Daiichi in 2011)

  11. Impact of Exercise on bones • “stresses” on mineral crystals cause bone growth • Increases in muscle mass increase both weight and tension on bones = growth • Ridges and bumps on bone relate to pull of tendons, diameter of bone relates to mass – • non-athletes have more fragile bones (osteoporosis and arthritis) • A broken leg with no stress, can lose 1/3 mass while using crutches • ? Bedridden and paralyzed

  12. Impact of Hormones on bones • Calcitrol: • made by kidneys • increases absorption of Ca and PO4 in digestive tract • Growth hormone • Made by pituitary • Stimulates osteoblast and synthesis of matrix • Thyroxine • Thyroid • Also stimulates osteoblasts and synthesis of matrix • Estrogen/ androgens • Ovaries and testes • Stimulates osteoblasts • Estrogen closes epiphysis earlier than androgens • Parathyroid hormone • Parathyroid glands • Stimulates osteoclasts and osteoblasts • Increases Ca level in body fluids • Calcitonin • Thyroid gland • Inhibits osteoclasts • Reduces Ca in body fluids • Triggers kidneys to loose calcium

  13. Impact of Nutrition on bones • Dietary sources of calcium and phosphate are required for healthy bone growth and maintenance • Also required are: magnesium, fluoride, iron and manganese • Vitamin C is needed for enzymatic reaction that makes cartilage • Vitamin D is required for calcitrol to cause intestinal absorption of Ca and PO4 • Vitamins A, K and B12 are also needed for normal bone growth

  14. Nutrition and Calcium • Bones are a mineral reservoir • 1-2 Kg of calcium ( 2.2 – 4.4 lbs) in body • 99% is in the bones • Calcium levels are important for many functions: • Permeability of plasma membranes • Firing of nerve impulses • Contraction of muscle fibers • Widely varying ion concentrations can result in seizures or death • “electrolytes”

  15. Figure 6-16a Factors That Alter the Concentration of Calcium Ions in Body Fluids Factors That Increase Blood Calcium Levels These responses are triggered when plasma calcium ion concentrations fall below 8.5 mg/dL. Low Calcium Ion Levels in Plasma (below 8.5 mg/dL) Parathyroid Gland Response Low calcium plasma levels cause the parathyroid glands to secrete parathyroid hormone (PTH). PTH Bone Response Intestinal Response Kidney Response Kidneys retain calcium ions Rate of intestinal absorption increases Osteoclasts stimulated to release stored calcium ions from bone more Osteoclast Bone calcitriol Calcium absorbed quickly Calcium conserved Calcium released Decreased calcium loss in urine ↑Ca2+ levels in bloodstream

  16. Figure 6-16b Factors That Alter the Concentration of Calcium Ions in Body Fluids Factors That Decrease Blood Calcium Levels HIgh Calcium Ion Levels in Plasma (above 11 mg/dL) These responses are triggered when plasma calcium ion concentrations rise above 11 mg/dL. Thyroid Gland Response Parafollicular cells (C cells) in the thryoid gland secrete calcitonin. Calcitonin Intestinal Response Bone Response Kidney Response Kidneys allow calcium loss Rate of intestinal absorption decreases Osteoclasts inhibited while osteoblasts continue to lock calcium ions in bone matrix less Bone calcitriol Calcium excreted Calcium absorbed slowly Calcium stored Increased calcium loss in urine ↓Ca2+ levels in bloodstream

  17. Fractures • Crack or break in bone • Often from stress in unusual direction • Need blood supply and portions of endosteum and periosteum in order to survive • Repair: • Spongy bone forms • External callus of cartilage stabilizes bone • Cartilage is replaced by bone • Remodeling removes dead bone or extra layers • Fracture types: • Transverse, displaced, compression, spiral, epiphyseal, communicated (shatter), greenstick

  18. Figure 6-17 Types of Fractures and Steps in Repair Epiphyseal fracture Compression fracture Transverse fracture Colles fracture Greenstick fracture Pott’s fracture Comminuated fracture Spiral fracture Displaced fracture Epiphyseal fractures, such as this fracture of the femur, tend to occur where the bone matrix is undergoing calcification and chondrocytes are dying. A clean transverse fracture along this line generally heals well. Unless carefully treated, fractures between the epiphysis and the epiphyseal cartilage can perman- ently stop growth at this site. Compression fractures occur in vertebrae subjected to extreme stresses, such as those produced by the forces that arise when you land on your seat in a fall. Transverse fractures, such as this fracture of the ulna, break a bone shaft across its long axis. Displaced fractures produce new and abnormal bone arrangements; nondisplaced fractures retain the normal alignment of the bones or fragments. Spiral fractures, such as this fracture of the tibia, are produced by twisting stresses that spread along the length of the bone. Comminuted fractures, such as this fracture of the femur, shatter the affected area into a multitude of bony fragments. A Colles fracture, a break in the distal portion of the radius, is typically the result of reaching out to cushion a fall. In a greenstick fracture, such as this fracture of the radius, only one side of the shaft is broken, and the other is bent. This type of fracture generally occurs in children, whose Long bones have yet to ossify fully. A Pott’s fracture occurs at the ankle and affects both bones of the leg. TYPES OF FRACTURES Fractures are named according to their external appearance, their location, and the nature of the crack or break in the bone. Important types of fractures are illustrated here by representative x-rays. The broadest general categories are closed fractures and open fractures. Closed, or simple, fractures are completely internal. They can be seen only on x-rays, because they do not involve a break in the skin. Open, or compound, fractures project through the skin. These fractures, which are obvious on inspection, are more dangerous than closed fractures, due to the possibility of infection or uncontrolled bleeding. Many fractures fall into more than one category, because the terms overlap. REPAIR OF AFRACTURE Fracture hematoma External callus Internal callus External callus Dead bone Bone fragments Spongy bone of external callus Periosteum A swelling initially marks the location of the fracture. Over time, this region will be remodeled, and little evidence of the fracture will remain. An internal callus forms as a network of spongy bone unites the inner edges, and an external callus of cartilage and bone stabilizes the outer edges. The cartilage of the external callus has been replaced by bone, and struts of spongy bone now united the broken ends. Fragments of dead bone and the areas of bone closest to the break have been removed and replaced. Immediately after the fracture, extensive bleeding occurs. Over a period of several hours, a large blood clot, or fracture hematoma, develops.

  19. Diseases and Disorders • Osteopenia = inadequate ossification • Aging ; begins between 30 and 40 • Lose 3% per decade • Vertebrae and jaw lose mass faster - spinal issues and loss of teeth • Osteoporosis – enough bone is lost to compromise normal function • Also related to decreasing estrogen and androgens • More of an issue in women because of menopause • Cancers

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