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Introduction to Bone and Bone Cells
Bone is often considered rigid and lifeless material. However, they are active parts of skeletal system and have numerous vital functions in living system.
Biologically, bone is dynamic connective tissue maintained by bone cells that make up skeletal system.
- Provides structural framework and support for body.
- Allows body movement and protects internal organs.
- Contributes to maintaining balance of minerals in our body.
Bone consists of extracellular matrix and bone cells. This combination makes bone active part of our overall physiological balance and bodily functions.
Bone cells are cellular components of bone tissue. Bone cells play important role in maintaining bone tissue, which, in turn, supports overall structure, movement, and mineral balance.
Found throughout skeletal system, bone cells contribute to dynamic and living nature of bones.
Types of Bone Cells
There are three main types of bone cells: osteoblasts, osteocytes, and osteoclasts.
Osteoblasts
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Bone-forming cells that constitute 4-6% of all bone cells.
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Located in growing areas of bone, such as endosteum and periosteum.
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Do not divide.
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Derived from precursor cells called osteoprogenitor or osteogenic cells that originate from pluripotent mesenchymal stem cells (MSCs) of bone marrow.
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Main function is to synthesize components of extracellular matrix of bone, including structural macromolecules like type I collagen, various proteoglycans, and proteins.
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Also involved in bone mineralization.
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After forming bone matrix, some osteoblasts get trapped in bone, transforming into osteocytes, while others become bone lining cells that cover bone surfaces.
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Remaining osteoblasts undergo programmed cell death known as apoptosis.
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Form bone matrix in two steps:
- First, by releasing substances like collagen proteins and proteoglycan to form initial organic matrix.
- Second, by mineralizing the matrix.
Osteoclasts
- Large, multinucleated bone-resorbing cells that break down old or damaged bone tissue.
- Secrete enzymes that dissolve matrix and organic components of bone.
- This resorption process is important for bone remodeling, repair, and maintaining mineral balance.
- Originate from white blood cells of hematopoietic stem cell lineage and are found on surface of bone tissue.
- Undergo process of recruitment, proliferation, differentiation, and fusion to carry out bone resorption function.
Osteocytes
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Mature bone cells that originate from osteoblasts.
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Found in small cavities called lacunae and are most abundant cells in mature adult bone tissue comprising about 90-95% of cells in bone.
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Result from osteoblasts that get surrounded and trapped by substances they secrete during bone formation.
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Have long lifespan of up to 25 years, and like osteoblasts, they do not divide.
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Serve vital roles in preserving mineral composition of bone tissue.
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Can deposit bone, signal other osteocytes about bone damage, and regulate activities of osteoblasts and osteoclasts.
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Communicate with one another through long channels in bone matrix called canaliculi, which are also used for transfer of nutrients and waste products.
Structure of Bone
Bones are made up of complex connective tissue comprised of bone cells and extracellular matrix.
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Matrix consists of about 60% inorganic components along with 10% water and 30% organic components.
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Organic component primarily made up of collagen along with proteoglycans, and non-collagenous proteins.
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Inorganic component contains hydroxyapatite crystals that contribute to hardness of bones.
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Bone consists of two main types of tissues:
- Cortical (compact) and cancellous (trabecular or spongy) bone.
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Compact bone is outer shell that surrounds inner spongy bone.
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Contains cylindrical-shaped structures called osteons or Haversian systems that consist of concentric lamellae with nerves and blood vessels.
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Compact bone provides shape, strength, and protection to bones.
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Beneath compact bone lies spongy bone which is porous and highly vascular internal tissue.
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Supports mineral exchange and maintains skeletal strength.
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Contains spaces filled with bone marrow.
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Outermost part is tissue layer called periosteum which covers external surface of cortical bone.
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On inner side, tissue layer called endosteum lines inner spongy bone tissue.
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Both periosteum and endosteum contain osteoprogenitor cells and are involved in bone development and repair.
Structure of Osteoblast
- Cuboidal or columnar cells found on bone surfaces with active bone formation.
- Have morphological features common in cells that synthesize proteins, such as prominent Golgi apparatus and abundant rough endoplasmic reticulum.
Structure of Osteoclasts
- Large cells with multiple nuclei derived from fusion of precursor cells.
- Have unique ruffled border. Ruffled border is rich in enzymes useful for breaking down bone minerals and matrix.
- Characterized by clear zone that creates acidic microenvironment for bone resorption.
Structure of Osteocytes
- Mature cells with flat and almond-shaped morphology.
- Have reduced Golgi complex and rough endoplasmic reticulum, along with more condensed nuclear chromatin.
- Extend long, hair-like cellular processes called dendrites into thin tubes known as canaliculi, forming network.
Functions of Bone Cells
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Osteoblasts contribute significantly to bone formation.
- Synthesize bone matrix to maintain structural shape of bone.
- Produce collagen and other organic components.
- Promote deposition of minerals into bone matrix, contributing to bone hardness.
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Osteoclasts are responsible for bone resorption.
- Play vital role in process of bone remodeling by breaking down bone tissue and releasing minerals like calcium and phosphate into bloodstream to support metabolic needs of body.
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Osteocytes play key role in maintaining bone tissue as they can sense mechanical stresses on bones.
- Involved in exchange of nutrients and waste products through network of canaliculi.
- Control osteoblastic and osteoclastic activities.
- Act as endocrine regulator of phosphate metabolism.
Bone Remodeling
Bones are dynamic structures constantly changing through process of bone remodeling. Bone remodeling is continuous process involving both removal of old or damaged bone and formation of new bone material.
This process contributes to development of mature structure of bone and regulation of calcium levels in body.
Bone remodeling is directed by bone multicellular units (BMUs), which are assemblies of osteoblasts and osteoclasts.
BMUs go through distinct phases:
- Activation phase - osteoclasts are recruited to targeted bone area.
- Resorption phase - osteoclasts break down or resorb bone tissue.
- Reversal stage - osteoclasts undergo apoptosis, and osteoblasts are called in.
- Formation stage - osteoblasts produce bone matrix that mineralizes, completing remodeling cycle.
Diseases and Disorders of Bone Cells
Various genetic and environmental factors contribute to different diseases of bone. Genetic abnormalities may result in weak bones.
- Nutritional deficiencies, especially in vitamin D, calcium, and phosphorus, can lead to poorly mineralized bone.
- Hormonal disorders, such as growth hormone deficiencies, can also affect bone health.
Osteoporosis
Age-related bone disease characterized by low bone mass and weak bone structure, increasing risk of fractures.
- Linked to imbalance between osteoblasts and osteoclasts.
- Common in postmenopausal females due to lower estrogen levels. Estrogen is known to be potent inhibitor of osteoclasts. However, it can affect males as well.
- Two main forms:
- Primary osteoporosis - most common form that occurs due to aging.
- Secondary osteoporosis - caused by other diseases or medications.
Rickets and Osteomalacia
Bone disorders caused by deficiency of vitamin D. Vitamin D is essential for calcium absorption and its deficiency impairs mineralization of growing bones.
- Rickets is disease affecting children that results from defect in depositing minerals in growing bones causing skeletal deformities, including bowed legs.
- Osteomalacia is adult equivalent of rickets which increases risk of fractures.
- Both conditions cause bone pain and significant muscle weakness.
- Adequate levels of vitamin D from sunlight, diet, or supplements are essential to prevent these conditions.
Paget’s Disease of Bone
Characterized by abnormal bone remodeling. While it can affect any bones, it often affects skull, pelvis, spine, and long bones.
- Main feature is disorganized bone remodeling, involving both excessive bone breakdown and increased bone formation.
- Makes affected bones larger and weaker than normal bones.
- Disorganized structure more likely to cause deformities or fractures.
- Can also lead to neurological complications.
Osteogenesis Imperfecta (OI)
Also called brittle bone disease, is group of inherited diseases that affect skeleton. These conditions result in bones that break easily.
- Different types arise from different genetic defects or mutations, impacting production of protein called type I collagen.
- Most forms are hereditary, although some cases may occur sporadically.
- People usually have low bone mass, which leads to more fractures and skeletal problems.
Osteopetrosis
Also called marble bone disease, is group of genetic disorders characterized by increased bone mass due to decrease in osteoclast function that is involved in resorption of bones.
- Disruption in bone resorption results in abnormal accumulation of dense bone.
- Despite density, bone is brittle, making individuals prone to fractures.
- Excessive bone growth may compress nerves causing neurological issues like deafness or blindness.
Summary
Bone is dynamic connective tissue of extracellular matrix 60% inorganic hydroxyapatite, 10% water, 30% organic collagen proteoglycans non-collagenous proteins and bone cells providing support, movement, organ protection and mineral balance. Three main bone cells are osteoblasts 4-6% cuboidal columnar from osteoprogenitor mesenchymal stem cells in periosteum endosteum synthesizing type I collagen and mineralizing matrix in two steps, some becoming osteocytes or lining cells others undergoing apoptosis, osteoclasts large multinucleated from hematopoietic white blood cells with ruffled border and clear zone creating acidic environment secreting enzymes for resorption via recruitment proliferation differentiation fusion releasing calcium phosphate, and osteocytes 90-95% most abundant in lacunae flat almond shaped with reduced Golgi RER condensed chromatin dendrites in canaliculi lifespan 25 years non-dividing sensing mechanical stress exchanging nutrients controlling osteoblasts osteoclasts regulating phosphate. Bone has cortical compact outer osteons Haversian systems with concentric lamellae nerves vessels and cancellous spongy inner porous vascular with marrow covered by periosteum and endosteum containing osteoprogenitors. Functions include osteoblasts formation and hardness, osteoclasts resorption and remodeling, osteocytes maintenance and endocrine regulation. Remodeling via bone multicellular units through activation, resorption, reversal, formation regulating calcium. Disorders include osteoporosis age-related low mass imbalance common postmenopausal low estrogen inhibitor of osteoclasts primary aging secondary disease medications, rickets in children bowed legs and osteomalacia adult from vitamin D deficiency impairing calcium absorption causing fractures pain weakness prevented by sunlight, Paget's abnormal disorganized remodeling larger weaker skull pelvis spine, osteogenesis imperfecta brittle bone from type I collagen mutations, and osteopetrosis marble bone from decreased osteoclast function dense brittle compressing nerves causing deafness blindness.
References
- Florencio-Silva R, Sasso GRS, Sasso-Cerri E, Simoes MJ, Cerri PS. Biology of Bone Tissue: Structure, Function and Factors. BioMed Research International. 2015. Volume 2015.
- Clarke B. Normal Bone Anatomy and Physiology. Clinical Journal of the American Society of Nephrology. 2008. Volume 3.
- Tortora GJ, Derrickson B. Principles of Anatomy and Physiology. 15th Edition. Wiley. Chapter 6, Bone Tissue and Bone Cells.
- Alberts B, Johnson A, Lewis J, Morgan D, Raff M, Roberts K, Walter P. Molecular Biology of the Cell. 6th Edition. Garland Science. Chapter 22, Bone Cells.
- Kini U, Nandeesh BN. Physiology and Pathology of Bone Remodeling. Journal of Clinical Pathology. 2012. Volume 65.
- Hadjidakis DJ, Androulakis II. Bone Remodeling. Annals of the New York Academy of Sciences. 2006. Volume 1092.
- Marks SC, Popoff SN. Bone Cell Biology: The Regulation of Development, Structure and Function. American Journal of Anatomy. 1988. Volume 183.
- Guyton AC, Hall JE. Textbook of Medical Physiology. 14th Edition. Elsevier. Chapter 79, Bone Cells.
- Kumar V, Abbas AK, Aster JC. Robbins and Cotran Pathologic Basis of Disease. 10th Edition. Elsevier. Chapter 26, Bone Disorders.
- Marieb EN, Hoehn K. Human Anatomy and Physiology. 11th Edition. Pearson. Chapter 6, Bones and Skeletal Tissues.
- Boyle WJ, Simonet WS, Lacey DL. Osteoclast Differentiation and Activation. Nature. 2003. Volume 423.
- Bonewald LF. The Amazing Osteocyte. Journal of Bone and Mineral Research. 2011. Volume 26.
- Forlino A, Marini JC. Osteogenesis Imperfecta. Lancet. 2016. Volume 387.
- Whyte MP. Paget's Disease of Bone and Genetic Disorders. New England Journal of Medicine. 2006. Volume 355.
- NCERT. Biology Textbook for Class XI. Reprint 2023-24. National Council of Educational Research and Training. Chapter 20, Locomotion and Movement.