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<oembed><version>1.0</version><provider_name>Future News 24</provider_name><provider_url>https://futurenews24.com</provider_url><author_name>Future News 24</author_name><author_url>https://futurenews24.com/index.php/author/mridulpahuja20/</author_url><title>PFKM acts as a metabolic swap initiating donut-shaped mitochondrial transforming to advertise osteogenesis - Future News 24</title><type>rich</type><width>600</width><height>338</height><html>&lt;blockquote class="wp-embedded-content" data-secret="sIiENFYKRV"&gt;&lt;a href="https://futurenews24.com/index.php/2026/08/31/s41368-026-00460-5/"&gt;PFKM acts as a metabolic swap initiating donut-shaped mitochondrial transforming to advertise osteogenesis&lt;/a&gt;&lt;/blockquote&gt;&lt;iframe sandbox="allow-scripts" security="restricted" src="https://futurenews24.com/index.php/2026/08/31/s41368-026-00460-5/embed/#?secret=sIiENFYKRV" width="600" height="338" title="&#x201C;PFKM acts as a metabolic swap initiating donut-shaped mitochondrial transforming to advertise osteogenesis&#x201D; &#x2014; Future News 24" data-secret="sIiENFYKRV" frameborder="0" marginwidth="0" marginheight="0" scrolling="no" class="wp-embedded-content"&gt;&lt;/iframe&gt;&lt;script&gt;
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</html><thumbnail_url>https://media.springernature.com/m685/springer-static/image/art%3A10.1038%2Fs41368-026-00460-5/MediaObjects/41368_2026_460_Fig1_HTML.png</thumbnail_url><thumbnail_width>1024</thumbnail_width><thumbnail_height>1024</thumbnail_height><description>Osteogenic differentiation requires sophisticated mitochondrial adaptation to meet bioenergetic demands, yet regulatory checkpoints governing this organelle reorganization remain poorly defined. Through single-cell RNA sequencing reanalysis and metabolic intervention, this study unveils a non-canonical signaling role for PFKM, traditionally recognized solely as a glycolytic enzyme, in orchestrating mitochondrial remodeling during bone formation. Beyond its established metabolic function, Pfkm suppression triggers distinctive donut-shaped mitochondria through a novel signaling cascade. Mechanistically, Pfkm knockdown expands mitochondria-endoplasmic reticulum contacts (MERCs), facilitating mitochondrial calcium influx. Concomitantly, elevated CD38 suppresses protein kinase A (PKA) activity, inducing DRP1 dephosphorylation at Serine 656. This signaling integration promotes DRP1 mitochondrial translocation, driving the characteristic donut architecture. This structural transformation initiates comprehensive mitochondrial quality control (MQC) encompassing enhanced biogenesis, selective mitophagy, and mitochondrial-derived vesicles (MDVs) secretion, collectively optimizing the osteogenic microenvironment and cellular mineralization capacity. In vivo validation demonstrates that AAV-mediated Pfkm knockdown accelerates bone repair in rat calvarial and femoral defect models. This work establishes PFKM as a dual-function regulator bridging metabolism and mitochondrial signaling, offering a potent therapeutic avenue for bone regeneration.</description></oembed>
