Key result
Cell cycle perturbation and serum deprivation induce fibroblast collagen production independently of type I collagen transcription.
Why the study?
The molecular pathways by which cardiac fibroblasts are activated during myocardial infarction recovery have not been fully elucidated.
Cell cycle perturbation induced by serum deprivation triggers collagen production in fibroblasts independently of transcription, revealing a novel mechanism for cardiac fibrosis post-myocardial infarction.
Should not change clinical practice; hypothesis-generating for post-transcriptional collagen regulation in fibroblasts.
Myocardial infarction (MI) occurs when the heart muscle is severely damaged due to a decrease in blood flow from the coronary arteries. During recovery from an MI, cardiac fibroblasts become activated and produce extracellular matrices, contributing to the wound healing process in the damaged heart. Inappropriate activation of the fibroblasts leads to excessive fibrosis in the heart. However, the molecular pathways by which cardiac fibroblasts are activated have not yet been fully elucidated.Here we show that serum deprivation, which recapitulates the cellular microenvironment of the MI area, strikingly induces collagen production in C3H/10T1/2 cells. Based on transcriptomic and pharmacological studies, we found that cell cycle perturbation is directly linked to collagen production in fibroblasts. Importantly, collagen synthesis is increased independently of the transcriptional levels of type I collagen genes. These results reveal a novel mode of fibroblast activation in the ischemic area, which will allow us to gain insights into the molecular mechanisms underlying cardiac fibrosis and establish a basis for anti-fibrotic therapy.
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Wake et al. (2019) studied Cardiac fibrosis. Serum deprivation and cell cycle perturbation vs. Normal serum conditions / untreated cells was evaluated on Collagen production (p=<0.05). Serum deprivation and pharmacological cell cycle perturbation significantly induced collagen production in C3H/10T1/2 fibroblasts independently of type I collagen gene transcription.
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