4.3 Review

Targeting cell-matrix interface mechanobiology by integrating AFM with fluorescence microscopy

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出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.pbiomolbio.2022.08.005

关键词

Atomic force microscopy; Nanomechanics; Mechanotransduction; Pericellular matrix; Cytoskeleton; Ion channels

资金

  1. National Science Foundation (NSF) [CMMI-1751898, CMMI-1826202]
  2. National Institutes of Health (NIH) [AR074490]
  3. Drexel University's Research and Engineering for Pediatrics by Inter-disciplinary Collaboration Leveraging Education and Partnerships for Pediatric Healthcare (R-EPIC LEAP for Pediatric Healthcare) from the U.S. Department of Education's Graduate Assistanc

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Mechanosensing at the interface of a cell and its surrounding microenvironment plays a crucial role in physiological processes. This review discusses the use of atomic force microscopy (AFM) integrated with immunofluorescence imaging to probe mechanobiology at the cell-matrix interface. It highlights the investigation of pericellular matrix biomechanics, cellular biomechanics, and mechanotransduction in various tissues. The review also presents technical advances that have facilitated more in-depth studies of mechanobiology.
Mechanosensing at the interface of a cell and its surrounding microenvironment is an essential driving force of physiological processes. Understanding molecular activities at the cell-matrix interface has the potential to provide novel targets for improving tissue regeneration and early disease intervention. In the past few decades, the advancement of atomic force microscopy (AFM) has offered a unique platform for probing mechanobiology at this crucial microdomain. In this review, we describe key advances under this topic through the use of an integrated system of AFM (as a biomechanical testing tool) with complementary immunofluorescence (IF) im-aging (as an in situ navigation system). We first describe the body of work investigating the micromechanics of the pericellular matrix (PCM), the immediate cell micro-niche, in healthy, diseased, and genetically modified tissues, with a focus on articular cartilage. We then summarize the key findings in understanding cellular biomechanics and mechanotransduction, in which, molecular mechanisms governing transmembrane ion channel-mediated mechanosensing, cytoskeleton remodeling, and nucleus remodeling have been studied in various cell and tissue types. Lastly, we provide an overview of major technical advances that have enabled more in-depth studies of mechanobiology, including the integration of AFM with a side-view microscope, multiple optomicroscopy, a fluorescence recovery after photobleaching (FRAP) module, and a tensile stretching device. The innovations described here have contributed greatly to advancing the fundamental knowledge of extracel-lular matrix biomechanics and cell mechanobiology for improved understanding, detection, and intervention of various diseases.

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