Baaba S. Otoo , Eng Kuan Moo , Amin Komeili , David A. Hart , Walter Herzog
{"title":"从波动到稳定:原位软骨细胞对循环压缩载荷的响应","authors":"Baaba S. Otoo , Eng Kuan Moo , Amin Komeili , David A. Hart , Walter Herzog","doi":"10.1016/j.jbiomech.2025.112734","DOIUrl":null,"url":null,"abstract":"<div><div>Chondrocytes, the sole cellular components in articular cartilage, are mechanosensitive and undergo significant morphological and volumetric changes in response to mechanical loading. These changes activate ion channels, initiating cellular mechanotransduction processes crucial for maintaining cartilage health. Dynamic loading has been shown to elicit anabolic responses that preserve cartilage integrity, while prolonged mechanical unloading leads to atrophy. However, the intricacies of how chondrocytes respond to dynamic loading remain poorly understood, largely due to technical limitations in capturing real-time cellular responses during loading cycles. This study aimed to advance our understanding of chondrocyte behavior during dynamic cyclic compression loading through high-speed imaging techniques. We developed a protocol to capture changes in chondrocyte volume, shape, and surface area at critical moments of maximal and minimal tissue stress during cyclic loading. Our findings revealed that chondrocyte volume fluctuated cyclically during the first 20 loading cycles, increasing by up to 4 % during load application and decreasing by as much as 8 % during unloading. These volume fluctuations stabilized over time, returning to baseline levels after approximately 100 cycles. Volume changes over time translate to shape change, causing similar oscillatory pattern in cell width and depth strains but not height strain, which remained relatively constant throughout the loading protocol. Changes in surface area mirrored the volume changes but were less pronounced (< 2 % increase), suggesting a protective mechanism against cell membrane rupture. This research offers valuable insights into the dynamic behavior of chondrocytes during cyclic loading, highlighting the importance of considering dynamic environments in cellular biomechanics studies.</div></div>","PeriodicalId":15168,"journal":{"name":"Journal of biomechanics","volume":"186 ","pages":"Article 112734"},"PeriodicalIF":2.4000,"publicationDate":"2025-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"From fluctuations to stability: In-Situ chondrocyte response to cyclic compressive loading\",\"authors\":\"Baaba S. Otoo , Eng Kuan Moo , Amin Komeili , David A. Hart , Walter Herzog\",\"doi\":\"10.1016/j.jbiomech.2025.112734\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Chondrocytes, the sole cellular components in articular cartilage, are mechanosensitive and undergo significant morphological and volumetric changes in response to mechanical loading. These changes activate ion channels, initiating cellular mechanotransduction processes crucial for maintaining cartilage health. Dynamic loading has been shown to elicit anabolic responses that preserve cartilage integrity, while prolonged mechanical unloading leads to atrophy. However, the intricacies of how chondrocytes respond to dynamic loading remain poorly understood, largely due to technical limitations in capturing real-time cellular responses during loading cycles. This study aimed to advance our understanding of chondrocyte behavior during dynamic cyclic compression loading through high-speed imaging techniques. We developed a protocol to capture changes in chondrocyte volume, shape, and surface area at critical moments of maximal and minimal tissue stress during cyclic loading. Our findings revealed that chondrocyte volume fluctuated cyclically during the first 20 loading cycles, increasing by up to 4 % during load application and decreasing by as much as 8 % during unloading. These volume fluctuations stabilized over time, returning to baseline levels after approximately 100 cycles. Volume changes over time translate to shape change, causing similar oscillatory pattern in cell width and depth strains but not height strain, which remained relatively constant throughout the loading protocol. Changes in surface area mirrored the volume changes but were less pronounced (< 2 % increase), suggesting a protective mechanism against cell membrane rupture. This research offers valuable insights into the dynamic behavior of chondrocytes during cyclic loading, highlighting the importance of considering dynamic environments in cellular biomechanics studies.</div></div>\",\"PeriodicalId\":15168,\"journal\":{\"name\":\"Journal of biomechanics\",\"volume\":\"186 \",\"pages\":\"Article 112734\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2025-04-29\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of biomechanics\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0021929025002465\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"BIOPHYSICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of biomechanics","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0021929025002465","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"BIOPHYSICS","Score":null,"Total":0}
From fluctuations to stability: In-Situ chondrocyte response to cyclic compressive loading
Chondrocytes, the sole cellular components in articular cartilage, are mechanosensitive and undergo significant morphological and volumetric changes in response to mechanical loading. These changes activate ion channels, initiating cellular mechanotransduction processes crucial for maintaining cartilage health. Dynamic loading has been shown to elicit anabolic responses that preserve cartilage integrity, while prolonged mechanical unloading leads to atrophy. However, the intricacies of how chondrocytes respond to dynamic loading remain poorly understood, largely due to technical limitations in capturing real-time cellular responses during loading cycles. This study aimed to advance our understanding of chondrocyte behavior during dynamic cyclic compression loading through high-speed imaging techniques. We developed a protocol to capture changes in chondrocyte volume, shape, and surface area at critical moments of maximal and minimal tissue stress during cyclic loading. Our findings revealed that chondrocyte volume fluctuated cyclically during the first 20 loading cycles, increasing by up to 4 % during load application and decreasing by as much as 8 % during unloading. These volume fluctuations stabilized over time, returning to baseline levels after approximately 100 cycles. Volume changes over time translate to shape change, causing similar oscillatory pattern in cell width and depth strains but not height strain, which remained relatively constant throughout the loading protocol. Changes in surface area mirrored the volume changes but were less pronounced (< 2 % increase), suggesting a protective mechanism against cell membrane rupture. This research offers valuable insights into the dynamic behavior of chondrocytes during cyclic loading, highlighting the importance of considering dynamic environments in cellular biomechanics studies.
期刊介绍:
The Journal of Biomechanics publishes reports of original and substantial findings using the principles of mechanics to explore biological problems. Analytical, as well as experimental papers may be submitted, and the journal accepts original articles, surveys and perspective articles (usually by Editorial invitation only), book reviews and letters to the Editor. The criteria for acceptance of manuscripts include excellence, novelty, significance, clarity, conciseness and interest to the readership.
Papers published in the journal may cover a wide range of topics in biomechanics, including, but not limited to:
-Fundamental Topics - Biomechanics of the musculoskeletal, cardiovascular, and respiratory systems, mechanics of hard and soft tissues, biofluid mechanics, mechanics of prostheses and implant-tissue interfaces, mechanics of cells.
-Cardiovascular and Respiratory Biomechanics - Mechanics of blood-flow, air-flow, mechanics of the soft tissues, flow-tissue or flow-prosthesis interactions.
-Cell Biomechanics - Biomechanic analyses of cells, membranes and sub-cellular structures; the relationship of the mechanical environment to cell and tissue response.
-Dental Biomechanics - Design and analysis of dental tissues and prostheses, mechanics of chewing.
-Functional Tissue Engineering - The role of biomechanical factors in engineered tissue replacements and regenerative medicine.
-Injury Biomechanics - Mechanics of impact and trauma, dynamics of man-machine interaction.
-Molecular Biomechanics - Mechanical analyses of biomolecules.
-Orthopedic Biomechanics - Mechanics of fracture and fracture fixation, mechanics of implants and implant fixation, mechanics of bones and joints, wear of natural and artificial joints.
-Rehabilitation Biomechanics - Analyses of gait, mechanics of prosthetics and orthotics.
-Sports Biomechanics - Mechanical analyses of sports performance.