Abstract

Pleiotrophin (PTN) is a widespread cytokine involved in bone formation, neurite outgrowth, and angiogenesis. In skeletal muscle, PTN is upregulated during myogenesis, post-synaptic induction, and regeneration after crushing, but little is known regarding its effects on muscle function. Here, we describe the effects of PTN on the slow-twitch soleus and fast-twitch extensor digitorum longus (EDL) muscles in mice over-expressing PTN under the control of a bone promoter. The mice were maintained in normal loading or disuse condition, induced by hindlimb unloading (HU) for 14 days. Effects of exposition to near-zero gravity during a 3-months spaceflight (SF) into the Mice Drawer System are also reported. In normal loading, PTN overexpression had no effect on muscle fiber cross-sectional area, but shifted soleus muscle toward a slower phenotype, as shown by an increased number of oxidative type 1 fibers, and increased gene expression of cytochrome c oxidase subunit IV and citrate synthase. The cytokine increased soleus and EDL capillary-to-fiber ratio. PTN overexpression did not prevent soleus muscle atrophy, slow-to-fast transition, and capillary regression induced by SF and HU. Nevertheless, PTN exerted various effects on sarcolemma ion channel expression/function and resting cytosolic Ca2+ concentration in soleus and EDL muscles, in normal loading and after HU. In conclusion, the results show very similar effects of HU and SF on mouse soleus muscle, including activation of specific gene programs. The EDL muscle is able to counterbalance this latter, probably by activating compensatory mechanisms. The numerous effects of PTN on muscle gene expression and functional parameters demonstrate the sensitivity of muscle fibers to the cytokine. Although little benefit was found in HU muscle disuse, PTN may emerge useful in various muscle diseases, because it exerts synergetic actions on muscle fibers and vessels, which could enforce oxidative metabolism and ameliorate muscle performance.

Highlights

  • Pleiotrophin (PTN), called heparin affin regulatory peptide (HARP), heparin binding-growth associated molecule (HB-GAM), or osteoblast stimulating factor-1 (OSF-1), is a heparin-binding cytokine expressed by several cell types during early differentiation and up-regulated after tissue injury [1]

  • To evaluate the effects of PTN overexpression on muscle fiber growth and atrophy induced by actual and simulated microgravity, the Cross Sectional Area (CSA) of Sol and Extensor Digitorum Longus (EDL) muscle fibers was measured on laminin-stained muscle (Fig. 1A)

  • PTN had no significant effect on muscle CSA in normal loading, and atrophy of Sol muscle was still observed in PTN mice either after hindlimb unloading (HU), with a 30% significant reduction of CSA, or after SF with a 32% CSA reduction

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Summary

Introduction

Pleiotrophin (PTN), called heparin affin regulatory peptide (HARP), heparin binding-growth associated molecule (HB-GAM), or osteoblast stimulating factor-1 (OSF-1), is a heparin-binding cytokine expressed by several cell types during early differentiation and up-regulated after tissue injury [1]. Since PTN over-expression in transgenic mice is associated with an increased bone mass and mineralization and may protect from experimentally-induced osteoporosis [8,9], the mice drawer system (MDS) experiment was designed to accommodate PTNoverexpressing mice aboard the International Space Station (ISS) with the aim to verify whether PTN can protect mice from space related osteoporosis [10]. In the MDS experiment, wild type and transgenic mice over-expressing PTN under the control of the human bone specific osteocalcin promoter were exposed to a nearzero gravity on board the ISS for a record-breaking period of three months. On return to Earth, analysis of bone microarchitecture in these mice revealed some protective effects of PTN against microgravity’s negative effects on weight-bearing bones, likely resulting from stimulation of osteoblast activity [11]

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