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Related Concept Videos

The Effect of Aging on Tissues01:19

The Effect of Aging on Tissues

Several body functions deteriorate with age. The external signs of aging are easily identifiable. For example, the skin becomes dry, less elastic, and thins out, forming wrinkles. The skin of the face begins to appear looser due to a decrease in the levels of elastic and collagen fibers in the connective tissue. Additionally, melanin production in the hair follicle decreases with age, resulting in gray hair. Moreover, the senses of sight and hearing decline, so glasses and hearing aids may...
Bone Disorders01:29

Bone Disorders

Aging and its effect on bone remodeling is the most common cause of bone disorders. In young and healthy people, bone deposition and resorption happen at an equal rate to maintain optimal bone health.
Bone deposition is also affected by the levels of sex hormones like estrogen and testosterone that promote osteoblast activity and bone matrix synthesis. When the level of these hormones decreases due to aging, it causes a reduction in bone deposition. As a result, bone resorption by osteoclasts...
Elastin is Responsible for Tissue Elasticity01:12

Elastin is Responsible for Tissue Elasticity

Elastic fiber contains the protein elastin along with lesser amounts of other proteins and glycoproteins. The main property of elastin is that it will return to its original shape after being stretched or compressed. Elastic fibers are prominent in elastic tissues found in skin and the elastic ligaments of the vertebral column.
Ligaments and tendons are made of dense regular connective tissue, but in ligaments not all fibers are parallel. Dense regular elastic tissue contains elastin fibers and...
Extracellular Matrix01:26

Extracellular Matrix

Unlike epithelial tissue, which is composed of cells closely packed with little or no extracellular space in between, connective tissue cells are dispersed in a matrix. This extracellular matrix (ECM) is composed of fibrous proteins like collagen, elastin, and fibronectin in a ground substance consisting of interstitial fluid, cell adhesion proteins, and proteoglycans. The proteoglycans form a gel-like material in the spaces between cells and provide hydration, buffering, binding, and force...
Growth of Cartilage and Bone Tissue01:27

Growth of Cartilage and Bone Tissue

Chondrocytes form a temporary cartilaginous model by dividing and secreting a thick gel-like extracellular matrix. Once the chondrocytes undergo programmed cell death, osteoblasts enter the site of the cartilaginous model. The process of replacing the temporary cartilaginous model with bone in an ordered manner is called endochondral ossification. In endochondral ossification, not all of the cartilage is replaced by bone tissue. Some cartilage that performs a protective and supportive function...
Degenerative Disc Disease I: Introduction01:27

Degenerative Disc Disease I: Introduction

Degenerative disc disease is a chronic condition in which intervertebral discs gradually lose structure and function. It is not infectious or autoimmune; rather, it results from age-related biochemical and mechanical changes, influenced by genetic, metabolic, and environmental factors.Structure and Function of DiscsThe spine contains 23 intervertebral discs that absorb load, distribute forces, maintain spacing, and allow flexibility. Each disc consists of a nucleus pulposus, a gel-like core...

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Application of Atomic Force Microscopy to Detect Early Osteoarthritis
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Published on: May 24, 2020

Aging-related differences in chondrocyte viscoelastic properties.

Nikolai Steklov1, Ajay Srivastava, K L P Sung

  • 1Shiley Center for Orthopaedic Research and Education at Scripps Clinic, North Torrey Pines Road, La Jolla, CA 92037, USA.

Molecular & Cellular Biomechanics : MCB
|June 5, 2009
PubMed
Summary

Aging significantly increases chondrocyte stiffness, impacting cell function and potentially contributing to cartilage degeneration. This age-related increase in cell stiffness, unlike osteoarthritis-related changes, may involve alterations in the cytoskeleton.

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Area of Science:

  • Biomedical Engineering
  • Cell Biology
  • Orthopedics

Background:

  • Articular cartilage biomechanics change with age, increasing osteoarthritis risk.
  • Chondrocyte biomechanical properties and their age-related changes are less understood.
  • Cell stiffness influences mechanotransduction and cellular function.

Purpose of the Study:

  • To investigate age-related changes in chondrocyte biomechanical properties.
  • To compare biomechanical properties between young and aged human chondrocytes.
  • To explore potential mechanisms behind altered cell stiffness with aging.

Main Methods:

  • Human chondrocytes isolated from knee cartilage (post-mortem or arthroplasty).
  • Cells grouped by age (18-35 years vs. 55+ years) and osteoarthritis grade (normal vs. osteoarthritic).
  • Micropipette cell aspiration technique used to measure viscoelastic properties (equilibrium modulus, instantaneous modulus, apparent viscosity).

Main Results:

  • Chondrocytes from the 55+ age group exhibited significantly higher equilibrium modulus, instantaneous modulus, and apparent viscosity compared to the 18-35 age group.
  • No significant differences in these biomechanical properties were observed between normal and osteoarthritic chondrocytes within the 55+ group.
  • Increased chondrocyte stiffness with aging is suggested to be linked to changes in the cell membrane, cytoplasm, or cytoskeleton.

Conclusions:

  • Advancing age leads to increased chondrocyte stiffness, independent of osteoarthritis severity.
  • This age-associated increase in cell stiffness may be mediated by cytoskeletal alterations, similar to mechanisms proposed for osteoarthritic chondrocytes.
  • Altered biomechanical properties of aging chondrocytes could impact cellular signaling and biochemical responses, potentially influencing cartilage health.