Bone Structures Flashcards
Load bearing structures of the mammal
Bone structures and cartilage wherever bones articulate with other bones.
Where is cartilage located?
Transition between bone and other connective tissue such as points of insertion of ligaments and tendons.
AND bone and bone articulation
Bones provide
Support, levers for locomotion, and provide protection (cranium for example- protection for the brain delicate tissues)
Also to house haemopoeitic tissues (bone marrow main haemopoietic tissue in adult animals)
Bones also have an important function calcium homeostasis- imp. reservoir of calcium. Maintain constant level of Ca in blood- imp. for funciton of all cells in the body (used to convey signals from cell membrane to the nucleus and other parts of the cell), muscle contractility as well.
Bone classification- 3 main
other ways?
Long bones- major limb bones- humerus, radius, etc
Short bones- vertebrae
Flat bones- skull bones, scapula
Other ways:
Cortical and trabeculae component
Cortical bone is compact.
Trabeculae bone- network of trabeculae or rods and plates- porous network
Periosteum
Dense connective tissue that surrounds bones. Not at articular surfaces. Interupted by tendons and ligaments
Endosteum
All surfaces inside a bone.
Shaft
Diaphysis- comprised of cotrical bone. Cylinder of bone with empty space in the middle with bone marrow
Very end of bone
Epiphysis- thin shell of cortical bone but primarily trabecular bone- shape varies enormously between individual bones and species. But generally rounded
Point at which shaft of the bone gets narrower is called?
Metaphysis- shape varies enormously. Made up of trabecular bone that turns into bone marrow- thin shell of cortical bone gets thicker.
Trabecular bone is normally contained by?
Thin layer of cortical bone
Blood supply to bone
Multiple sources. Bone in a living animal is a dynamic living tissues. Bone is constantly being turned over by cells.
Major source of blood supply: nutrient artery (nutrient foramen) into the bone marrow- branches which pass into cortical bone- (diaphysis)- nutrient artery anastomose as well
Metaphyseal and epiphyseal arteries
Adult animal- arteries anastamose inside the bone.
If you didn’t have anastamose- large areas of bone would just die.
The anastamose does not happen until animals are fully grown, fully mature.
Medullary vein- (medulla is marrow)- veins leave the bone accompanying the nutrient artery accompanying the epiphyseal and metaphyseal.
Growth plate
Made of cartilage- can tell if adult bone or juvenile- not fully matured
How do the bones drain?
Veins leave the bone accompanying the nutrient artery and metaphyseal and epiphyseal vessels
Cortical bone of diaphysis drains to the periosteal veins
Centrifigal blood through the cortical bone of the diaphysis
Draining into the periostial venules
What is bone comprised of?
Connective tissue.
Extracellular matrix
Cellular component
What are the two components of the bone matrix?
Organic (type I collagen- fibres of type I which is THICK collagen fibres, glycoproteins mixed in, many of them are there because they have the capacity to bind Ca2+
inorganic component (mineral- hydroxyappetite- calcium and phosphate)
Both proteinaceous and mineral arranged in layers. Lamella bone- mature bone in which the bone matrix is arranged in layers.
When first formed in an embryo or in pathological process- they are randomly arranged, collagen not parallel- less organization. THIS IS CALLED WOVEN BONE.
Osteoblasts
Osteoblasts- cuboidal cells that have the function of synthesizing and secreting bone matrix
Situation where there is mature bone and they form lamilla bone- they secrete bone matrix on which they are adherent to.
Collagen type I and calcium binding proteins- called ostoid (?)
Within a few days ostioid is mineralized.
Successive layers of bone matrix deposited on bone surfaces. When osteoblasts mature they differentiate into osteocytes and are embedded into matrix.
Osteocytes
A bit shrunken compared to osteoblasts
Osteoblasts- Substantial RER because they are actively synthesizing proteins to secrete- as they diff. into osteocytes they become less active in synthesis and they shrink- less cytoplasm. But what they have is organized into multiple processes which extend out into channels in the bone called cuniliculi– the osteocytes located in the space within the bone called a lacuna. Extending out are multiple cuniliculi (sp)- osteocyte processes make contact with other osteocytes and form gap junctions. With osteoblasts as well.
Osteocytes are thought to transmit signals within the bone.
Bones are responsive to mechanical loading and they adapt their structure to forces they are exposed to.
Bone lining cells
Bone surfaces in general are covered with one type of cell or another. Active cell formation then osteoblasts. Esp in adult animals- there are few osteoblasts. Vast majority are covered in bone lining cells- capacity to differentiate into osteoblasts
Osteoclasts
Small proportion. Changes depending on level of bone turnover taking place.
Multinucleate
Capacity to resorb bone (dissolve bone matrix)
Old bone with small cracks in it can be removed and replaced by new bone.
They are also important in new growth- keep removing bone on inside so marrow cavity can expand.
They do that by adheringt o bone surfaces by ceiling zone- forms a ring around the outside between the osteoclasts and the bone surface- seals off an microenvironment. Described as apical surface- the osteoclasts secrete hydrogen ions to acidify the microenvironment which provides the right conditions for lysosomal enzymes secreted into micro environment. These enzymes are proteolytic break down collagen fibres and the bone.
Osteoclasts are the only cells taht can resorb bone and degrade the bone matrix.
Where is bone marrow? What is it made up of?
Diaphysis hollow cylinder.
Haemopoeitic tissue.
Also adipose tissue
Trabecular bone
No blood vessels, except some large species because they are actually really thick and need it. Generally gets it blood supply from vessels from the marrow supply.
How is trabecular bone structured?
Network of plates and rods
Homogenous pink stain- bone tissue (osteocytes scattered) amongst bone marrow
Bone in 3D- lumbar vertebrae- microcomputertomography- mouse bone- you can see the plate like structures connected by rod like structures- connected
Cortical bone- structure
Osteon (Haversian system)- longitudinal cylinders of bone tissues consisting concentric bone lamilae arranged around central canal containing a blood vessel (arteriole and venule) AND nerve branches.
(note the transverse canals connecting vessels- Volkmann’s canals)
**Concentric layers of collagen fibres surrounding Haversian canal- arranged at right angles to each other– enormous strength of osteons.
Spider like structures- osteocyte lacuni. Cuniliculi extending out from them- osteocytes to osteocytes and their gap junctions.
Osteons are different sizes. Dark profile. Volkman’s canal connecting two Haversian canal. You can also see the tiny cuniliculi.
Cortical bone
Dense, compact. You can see some blood vessels and osteocytes. You can also see osteoblasts if immature (or damaged). Some trabecular bone scattered amongst bone marrow.
Mesenchymal stem cell
Capacity to diff. to adipose, cartilage, muscle, fibroblasts, or osteoblasts, osteocytes or bone lining cells
* Adult stem cells- persist in adult animals- they cannot diff into all diff tissues but still many of them- predominantly muscle
Osteoblast Differentiation
Active osteoblasts- synthesize and secrete bone matrix (ostioid)
3 possibilities:
- terminal differentiation into osteocytes and retained within bone tissue
- Apoptosis- if excess of osteoblasts
- Bone lining cells- no requirement to form new bone but could if needed. Resting cells. Form barrier between bone matrix sufrace and surrounding tissues.
Intramembranous ossification
The way the flat bones develop
e. g. skull
1. Condensation of embryonic mesenchymal cells- (condensation means- accumulation of mesenchymal cells close to each other happens through prolif and cell migration)
2. As they condense they diff. into osteoblasts
3. Then they secrete ostioid
4. Then it starts to mineralize
Bottom picture- you can see growing trabecular matrix. Edges of pre-existing spicules- new ostioid being deposited. Gradually expand. They start to fill in trabecular and gradually form thin cortical shell.
e.g. mouse skull would just be cortical bone structure
Cartilage purposes
Support where flexibility is required
Shock absorption
Articular cartilage- smooth articular surface- bones move in relation to each other within synovial joints
Composed of cells and extracellular material
Hyaline Cartilage (one of three types)
Growth plates
Articular surfaces
e.g. Tracheal cartilage (rapidly growing lamb)- picture
Perichondrium- dense connective tissue surrounding cartilage
As cartilage grows and get larger- they separate
Trachea- randomly arranged cells
Growth plate- they are not randomly arranged- chondrocytes are in an organized columnar structure
Hyaline cartilage- has a high ratio of fibres!! It looks homogenous there is SO MUCH. (Glycosaminoglycans)
Blood in Cartilage
Avascular in normal adult mammal
Tracheal cartilage is usually avascular
There are exceptions- esp. in large animals with large masses of cartilage there will be blood vessels
Mostly related to articular cartilage
Chondrocyte
Only cell present in healthy cartilage
Present encased in lacuni
Normally fill lacuna
Individual chondrocytes would be on their own. Interstitial growth is possible in cartilage- grows through prolif. of chondrocytes. So they congregate if this is going on.
Cartilage Extracellular Matrix
Synthesized and secreted by chondrocytes
Made up of fibres and amorphous material
Fibres are composed of collagen type II- only present in cartilage and almost no other locations.
Fibres forming teh skeleton of the cartilage structure- packed in amongs fibres is the amorphous EC material. Proteoglycans and Hyaluronan.
Proteoglycan and Hyaluronan- purpose? structure?
Many proteoglycan molecules linked to hyaluronan molecules.
Side chains are negatively charged- hydrophilic- attract water- packed in amongst collagen fibres- swelling against the pressure of the compression of the collagen fibres. This provides the shock absorption
Elastic cartilage
External ear and epiglottis
Places where more flexibility is required
Elastic fibres in the matrix
Perichondrion
Fibrocartilage
Intervertebral discs, TMJ, manisci (sp?) at attachments of ligaments and joints Also in the cardiac skeleton as well
Providing structural transition between rigid hard tissue of bone and the flexible tissue of ligament or tendon
If you had a sudden transition from flexible to rigid in some locations this would result in stresses and damage of soft tissue
(lower ratio of glycosaminoglycans- fibres to collagen fibres- for that reason- you can see the fibres in the fibrocartilage. Chondrocytes are arranged in rows and columbs between the fibres)
Endochondral ossification
ALL bones develop this way except for flat bones. (Long bones and short bones)
Involves formation of cartilage model
Generalized mesenchyme- instead of cells diff. directly. They undergo condensation. They then diff. into chondrocytes- synthesize cartilage matrix. And then they go on and form the model of the future bone.
Basic shape- chondrocytes of the future diaphysis start to undergo hypertrophy. The lacuna around them expands (they digest away) creates signals that lead to the deposition of a thin layer of bone around the outside of the midshaft of the bone:
Periostial bone collar- forms around the outside. Once the PBC is there. Diff. of osteoblasts around the outside of cartilage model which lay down bone. Again after the PBC, all of the necessary cell types start to invade into the spaces that the hypertrophic chondrocytes created. Osteoclasts come in and start to break down cartilage matrix freeing up path for osteoblast and bone marrow precursors to invade.
If chondrocytes are flattened- they have just recently proliferated– as they mature a bit then they start to secrete cartilage matrix and they start to separate from each other. They will die– empty lacuni where the blood vessels and osteoclasts can get into.
Endochondral ossification
- Cartilage model
- Invasion of primary centre of ossification
- Once it forms- it gradually expands towards each end of the bone with proliferation of chondrocytes in the remaining cartilage. Bone expands in length and at the same time primary centre of ossification is expanding. Remanants of cartilage- osteoblasts deposit bone on. Continues to lengthen the bone throug prolif of chondrocytes.
- Most long bones formation of secondary centre of ossification at both ends. through similar process to primary ossification. NOT in SHORT BONES. Don’t need the longitudinal growth- just widening. When you get the secondary centre there is still cartilage left- THIS IS WHAT IS CALLED THE GROWTH PLATE. The Growth plate continues to take over the growth plate cartilage. Cartilage loses the race, give up, and the metaphyseal bone takes over and fuses to the epiphysis. This is when bone growth ceases (gradual process). (growth plate gets thinner and thinner as animals get older- secondary ossification centre first forms it is thick, but gets thinner fairly rapidly– animal approaching puberty- quite thin)
- Mature bone- just articular cartilage left at the end on the surface.
What causes longitudinal Growth of Bones??
Proliferation of chondrocytes!!
Matrix of chondrocytes and hypertrophy of chondrocytes as well
Point out some structures
Note columns of chondrocytes. At the base= hypertrophy= and even further down they die. Cells of ossification front below that
Some places you start to lose transverse struts of chondrocyte lacuni- but in the vertical ones stay intact. Vertical struts provide structure for osteoblasts to deposit bone matrix. Also vessels in there.
Pale staining in the middle of trabecular- vertical remnants of vertical struts. Bone matrix that osteoblasts have laid down on top of vertical struts.
Regulation of endochondral ossification
Behaviour of chondrocytes is key.
Circulating hormones and locally secreted factors. Growth hormone is really imp. Acts in 2 ways. Stim secretion of insulin like growth factor 1- acts on receptors on chondrocytes. Chondrocytes also secrete IGF 1- stim. proliferation. BMPs- stim. chondrocyte prolif in growth plate.
Important break that is acting at the same time- ensure it doesnt get out of hand. Provided by fibroblast growth factors (inhibit proliferation)
Thyroid hormones from the thyroid gland regulate the hypertrophy of the chondrocytes. Also stim. release of IGF1 and fibroblast growth factors. Also add to chondrocyte hypertrophy. Inhibit release of parathyroid hormone (PTHrP)- closely related to thyroid hormone. Produced localled by chondrocytes- inhibits hypertrophy.
Cartilage matrix secretion regulation- need nice solid cartilage structure for stable growth plate- also stimulated by IGF 1 and BMPs
Hypertrophic chondrocytes secrete factors that regulate behaviour of ossificiation front- chondrocytes that are closest to the front- secrete vascular endothelial growth factor- factor that stimulates angiogenesis. blood vessels are the first structures that invade ahead of the osteoclasts- clear a path and ensure appropriate nutrition for bone cellst aht follow them
RANKL- factor that is essential for osteoclast differentiation. Hypertrophic chondrocytes secreting RANKL- stim. differentiation and activity of osteoclasts on the ossification front.
BMPs- Also stim. osteoblast differentiation and bone matrix synthesis.
Only works properly in normal animals- stimulation and BRAKE. Appropriate balance.
Mutations in any regulatory factor leads to?
Skeletal dysplasia- abnormal growth of the skeleton. Chondral dysplasia (dysplasia of growth cartilage).
Range of genes that can mutate and cause pathology: Genes encoding cartilage matrix proteins, hormones, growth factors, or growth factor receptors, or the mediators.
e.g. Bulldog dwarfism (in calves)- severe, short legged phenotype (Dachshunds- considered chondrodysplasia)- Fibroblast growth factor 4- fibroblast growth factors suppress chondrocyte proliferation
Proximal
Structures that lie towards the junction with the body
Distal
Structures further away from the junction of the limb with the body
Cranial and caudal of the limb
The front and the back of the limb if proximal to the carpus or tarsus
Dorsal and palmar
the front and back of the forelimb from the carpus distally
Dorsal and plantar
The front and back of the hindlimb from the tarsus distally
Axial and abaxial
Towards the axis or midline of the limb; away from the axis of the limb
What is a ventrodorsal projection or view of the abdomen, for example?
The beam enters the abdomen ventrally and exits dorsally. The animal will be lying in dorsal recumbency (on its back).
When radiographed, an animal in left lateral recumbency produces what? And how are they lying?
Right side up, left side down.
Produces left lateral projection
Dorsal flexion
Some joints such as the metacarpophalangeal and metatarsophalangeal joints in the dog are in a state of overextension or dorsal flexion at rest. In these joints, flexion will increase the dorsal angle of this joint and extension will decrease the angle. Further or hyperextension of this joint is also referred to as dorsi- or dorsal flexion.
What is the metacarpo or metatarsophalangeal joint commonly known as in the horse?
Fetlock joints
Hyperextension
Movement beyond the normal range of extension
Abduction
A movement that pulls a structure away from the midline of the body
Adduction
A movement that pulls a structure towards the midlne of the body
Circumduction
When an extremity is moved in the curved plane of the surface of a cone- the joint that allows this motion must therefore allow abduction, adduction, flexion, and extension.
What is an example of a joint and circumduction? In your index finger?
Ball and socket joints- e.g. humerus or carpometacarpal joint
Sliding and Gliding in joints
Joint surfaces slide transversely across the opposing surface. Most synovial joints- range normally restricted by ligaments stabilizing the joint
Rotation
Circular movement of a part such as a bone around its long axis- e.g. in a quadruped when tilting its head to one side- chiefly involves the atlanto axial joint (upper part of the neck between the first and second vertebrae- the atlas and axis)
Pronation
Inward rotation of the forepaw that allows the palmar surface to face outwards
Supination
An outward rotation of the forelimb so that the palmar surface faces inwards
Eversion
The plantar surface of the hindlimb is turned to face laterally (outwards)- requires both pronation and abduction of the metatarsus
Inversion
The plantar surface of the hindlimb is turned to face medially (inwards)- requires supination and adduction of the metatarsus
Fibrous joints- 3 types
Type 1: Syndesmosis
Lots of intervening connective tissue e.g. connection of the hyoid to the skull in the dog
Fibrous joints- 3 types
Type 2: Suture
Mostly occur within the skull
Fibrous joints- 3 types
type 3: Gomphosis
The implantation of a tooth in its socket
Cartilaginous: 2 types
Hyaline- usually temporary such as the epiphyseal plate (growth plate), but also costochondral junctions that remain cartilaginous through life
Fibrocartilaginous- e.g. pelvic and mandibular symphyses
Synovial
These joints have a joint cavity containing synovial fluid, a joint capsule (outer fibrous and inner synovial membrane), and articular cartilage. A synovial joint may be simple: has two articular surfaces e.g. the shoulder joint OR compound: has more than two articular surfaces within the same joint capsule e.g. elbow, stifle.