Penicillin–streptomycin influences macrophage mechanical properties and microenvironment mechano-sensation

Penicillin-streptomycin (pen-strep) is routinely included in cell culture media, yet its impact on macrophage mechanics has not been systematically examined. Here, we show that pen-strep treatment increases macrophage stiffness in a time-dependent manner, while adhesion strength is only transiently affected. Morphological analysis revealed that pen-strep promotes cell spreading on PDMS rubber, collagen I, laminin, poly-amino acids, and poly-RGD peptides, but reduces spreading on type IV collagen, indicating altered extracellular matrix sensing in a context-dependent fashion. Gene expression assays further demonstrated upregulation of YAP-1 and TAZ and downregulation of β1 integrin, consistent with reprogramming of mechanotransduction pathways. Consequently, pen-strep elevated intracellular ROS, suppressed the M1 gene spectrum, induced heterogeneous M2-associated responses, and impaired phagocytic capacity. Collectively, these findings identify pen-strep as a modulator of macrophage stiffness, ECM mechano-sensation, polarization, and key immune functions, raising concerns about its routine use in mechanobiology research and clinical applications.

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Publication Details

Journal
Mechanobiology in Medicine
Published
2025-12-31
DOI
https://doi.org/10.1016/j.mbm.2025.100173
Citations
1
Primary Topic
Cellular Mechanics and Interactions
Type
article
Field-Weighted Citation Impact
1.15
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Penicillin–streptomycin influences macrophage mechanical properties and microenvironment mechano-sensation

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article

Penicillin–streptomycin influences macrophage mechanical properties and microenvironment mechano-sensation

Buwei Hu, Yufan Zheng, Jing Yang, Rui Liu, Yang Song, Shiqi Hu
article en
1 citations

Abstract

Penicillin-streptomycin (pen-strep) is routinely included in cell culture media, yet its impact on macrophage mechanics has not been systematically examined. Here, we show that pen-strep treatment increases macrophage stiffness in a time-dependent manner, while adhesion strength is only transiently affected. Morphological analysis revealed that pen-strep promotes cell spreading on PDMS rubber, collagen I, laminin, poly-amino acids, and poly-RGD peptides, but reduces spreading on type IV collagen, indicating altered extracellular matrix sensing in a context-dependent fashion. Gene expression assays further demonstrated upregulation of YAP-1 and TAZ and downregulation of β1 integrin, consistent with reprogramming of mechanotransduction pathways. Consequently, pen-strep elevated intracellular ROS, suppressed the M1 gene spectrum, induced heterogeneous M2-associated responses, and impaired phagocytic capacity. Collectively, these findings identify pen-strep as a modulator of macrophage stiffness, ECM mechano-sensation, polarization, and key immune functions, raising concerns about its routine use in mechanobiology research and clinical applications.

Mechanobiology in MedicineVol. 4(1)
University of California, Los Angeles (US), Fudan University (CN), West China Medical Center of Sichuan University (CN)
Openalex Percentile: Top 17%
Cellular Mechanics and Interactions
1.15
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