• 제목/요약/키워드: Traction force microscopy

검색결과 6건 처리시간 0.022초

Traction force microscopy for understanding cellular mechanotransduction

  • Hur, Sung Sik;Jeong, Ji Hoon;Ban, Myung Jin;Park, Jae Hong;Yoon, Jeong Kyo;Hwang, Yongsung
    • BMB Reports
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    • 제53권2호
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    • pp.74-81
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    • 2020
  • Under physiological and pathological conditions, mechanical forces generated from cells themselves or transmitted from extracellular matrix (ECM) through focal adhesions (FAs) and adherens junctions (AJs) are known to play a significant role in regulating various cell behaviors. Substantial progresses have been made in the field of mechanobiology towards novel methods to understand how cells are able to sense and adapt to these mechanical forces over the years. To address these issues, this review will discuss recent advancements of traction force microscopy (TFM), intracellular force microscopy (IFM), and monolayer stress microscopy (MSM) to measure multiple aspects of cellular forces exerted by cells at cell-ECM and cell-cell junctional intracellular interfaces. We will also highlight how these methods can elucidate the roles of mechanical forces at interfaces of cell-cell/cell-ECM in regulating various cellular functions.

세포군집의 확장에 관여하는 물리적 힘의 가시화 (Visualization of mechanical stresses in expanding cell cluster)

  • 조영빈;권보미;고웅현;신현정
    • 한국가시화정보학회지
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    • 제13권1호
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    • pp.43-48
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    • 2015
  • Collective cell migration is a fundamental phenomenon observed in various biological processes such as development, wound healing, and cancer metastasis. During the collective migration, cells undergo changes in their phenotypes from those of stable to the migratory state via the process called epithelial-mesenchymal transition (EMT). Recent findings in biology and biochemistry have shown that EMT is closely related to the cancer invasion or metastasis, but not much of the correlations in kinematics and physical forces between the neighboring cells are known yet. In this study, we aim to understand the cell migration and stress distribution within the expanding cell cluster. We constructed the in vitro cell cluster on the hydrogel, employed traction force microscopy (TFM) and monolayer stress microscopy (MSM) to visualize the physical forces within the expanding cell monolayer. During the expansion, cells at the cluster edge exhibited enhanced motility and developed focal adhesions that are the essential features of EMT while cells at the core of the cluster maintained the epithelial characteristics. In the aspect of mechanical stress, the cluster edge had the highest traction force of ~90 Pa directed toward the cluster core, which means that cells at the edge actively pull the substrate to make the cluster expansion. The cluster core of the tightly confined cells by neighboring cells had a lower traction force value (~60 Pa) but the highest intercellular normal stress of ~800 Pa because of the accumulation of traction from the edge of the monolayer.

PIV 및 TFM 측정 기법을 이용한 예쁜꼬마선충의 동적 패턴 가시화 연구 (Characterization of Dynamic Behavior of C. elegans in Different Physical Environments)

  • 박진성;윤병환;신현정
    • 한국가시화정보학회지
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    • 제12권2호
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    • pp.18-22
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    • 2014
  • Caenorhabditis elegans (C. elegans) is an undulatory nematode which exhibits two distinct locomotion types of swimming and crawling. Although in its natural habitat C. elegans lives in a non-Newtonian fluidic environment, our current understanding has been limited to the behavior of C. elegans in a simple Newtonian fluid. Here, we present some experimental results on the penetrating behavior of C. elegans at the interface from liquid to solid environment. Once C. elegans, which otherwise swims freely in a liquid, makes a contact to the solid gel boundary, it begins to penetrate vertically to the surface by changing its stroke motion characterized by a stiffer body shape and a slow stroke frequency. The particle image velocimetry (PIV) analysis reveals the flow streamlines produced by the stroke of worm. For the worm that crawls on a solid surface, we utilize a technique of traction force microscopy (TFM) to find that the crawling nematode forms localized force islands along the body where makes direct contacts to the gel surface.

미세아교세포의 진동 거동의 연구 (Oscillatory behavior of microglial cells)

  • 박은영;조영빈;고웅현;박진성;신현정
    • 한국가시화정보학회지
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    • 제19권1호
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    • pp.74-80
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    • 2021
  • Cells regulate their shapes and motility by sensing the cues from the internal and external microenvironment. Under different circumstances, microglia, the brain resident immune cells, undergo dynamic phenotypic changes, one of which is a remarkable periodic oscillatory migration in vitro. However, very little is known about the kinematic and dynamic perspectives of this oscillatory behavior. In this study, we tracked the changes in cell morphology and nuclear displacement, and visualized the forces using traction force microscopy (TFM). By correlation analyses, we confirmed that the lamellipodia formation preceded the nuclear translocation. Moreover, traction, developed following lamellipodia formation, was found to be localized and fluctuated at two ends of the oscillating cells. Taken together, our results imply that oscillatory microglial cells feature a viscoelastic migration, which will contribute to the field of cell mechanics.

골격근 손상 및 재생 환경에서의 근육 세포 군집 이동의 물리적 특성 가시화 (Visualization of the physical characteristics of collective myoblast migration upon skeletal muscle injury and regeneration environment)

  • 권태윤;정현태;조영빈;신현정
    • 한국가시화정보학회지
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    • 제20권2호
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    • pp.70-77
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    • 2022
  • Skeletal muscle tissues feature cellular heterogeneity, including differentiated myofibers, myoblasts, and satellite cells. Thanks to the presence of undifferentiated myoblasts and satellite cells, skeletal muscle tissues can self-regenerate after injury. In skeletal muscle regeneration, the collective motions among these cell types must play a significant role, but little is known about the dynamic collective behavior during the regeneration. In this study, we constructed in vitro platform to visualize the migration behavior of skeletal muscle cells in specific conditions that mimic the biochemical environment of injured skeletal muscles. We then visualized the spatiotemporal distribution of stresses arising from the differential collectiveness in the cellular clusters under different conditions. From these analyses, we identified that the heterogeneous population of muscle cells exhibited distinct collective migration patterns in the injury-mimicking condition, suggesting selective activation of a specific cell type by the biochemical cues from the injured skeletal muscles.

가교제 증량이 트레드용 실리카 컴파운드의 물성에 미치는 영향 (Physical Properties of the Silica-Reinforced Tire Tread Compounds by the Increased Amount of Vulcanization Agents)

  • 서병호;김기현;김원호
    • Elastomers and Composites
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    • 제48권3호
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    • pp.201-208
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    • 2013
  • 본 연구는 황과 가교 촉진제의 함량이 달리 적용된 acrylonitrile styrene-butadiene rubber (AN-SBR)/silica 컴파운드가 타이어 트레드 컴파운드의 특성에 미치는 영향에 대해 연구하였다. 실험 결과, 가교제 및 가교촉진제의 함량이 증가할수록 가교 반응성이 증대되어 가교속도 및 컴파운드의 가교도가 상승하였다. 또한 내마모 특성 뿐만 아니라 경도, 모듈러스와 같은 컴파운드의 기계적 특성은 높은 가교도에 기인하여 향상되었다. 동적 점탄 특성에서는 가교도의 증가와 함께 유리전이온도 ($T_g$)가 상승하여 $0^{\circ}C$ 영역에서의 tan ${\delta}$ 값이 향상되었고, $60^{\circ}C$ 영역에서의 tan ${\delta}$ 값이 감소되었다. 초기 가교 속도 ($t_1$)는 $60^{\circ}C$의 tan ${\delta}$ 값과 선형적인 관계를 나타내었다. 이는 가교제의 증량으로 초기 가교 속도 ($t_1$)가 빨라져 조기에 가교가 시작됨으로써 filler network 의 발달을 억제시킨 결과에 따른 것으로 판단된다. 이러한 결과는 AFM (atomic force microscopy)을 통하여 열처리된 컴파운드의 표면 관찰에서도 확인할 수 있었다. 따라서, 빠른 초기 가황 반응에 기인한 실리카의 re-agglomeration 감소는 $60^{\circ}C$에서의 tan ${\delta}$를 결정하는 매우 중요한 변수임을 알 수 있다.