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Pyrintegrin Induces Soft Tissue Formation by Transplanted or Endogenous Cells

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ABSTRACT

Focal adipose deficiency, such as lipoatrophy, lumpectomy or facial trauma, is a formidable challenge in reconstructive medicine, and yet scarcely investigated in experimental studies. Here, we report that Pyrintegrin (Ptn), a 2,4-disubstituted pyrimidine known to promote embryonic stem cells survival, is robustly adipogenic and induces postnatal adipose tissue formation in vivo of transplanted adipose stem/progenitor cells (ASCs) and recruited endogenous cells. In vitro, Ptn stimulated human adipose tissue derived ASCs to differentiate into lipid-laden adipocytes by upregulating peroxisome proliferator-activated receptor (PPARγ) and CCAAT/enhancer-binding protein-α (C/EBPα), with differentiated cells increasingly secreting adiponectin, leptin, glycerol and total triglycerides. Ptn-primed human ASCs seeded in 3D-bioprinted biomaterial scaffolds yielded newly formed adipose tissue that expressed human PPARγ, when transplanted into the dorsum of athymic mice. Remarkably, Ptn-adsorbed 3D scaffolds implanted in the inguinal fat pad had enhanced adipose tissue formation, suggesting Ptn’s ability to induce in situ adipogenesis of endogenous cells. Ptn promoted adipogenesis by upregulating PPARγ and C/EBPα not only in adipogenesis induction medium, but also in chemically defined medium specifically for osteogenesis, and concurrently attenuated Runx2 and Osx via BMP-mediated SMAD1/5 phosphorylation. These findings suggest Ptn’s novel role as an adipogenesis inducer with a therapeutic potential in soft tissue reconstruction and augmentation.

To read the full article click HERE.

Date of publication: 27 January 2017; Nature: Scientific Reports 7

Author information: Bhranti S. Shah (1,2); Mo Chen ()1; Takahiro Suzuki (1); Mildred Embree (1); Kimi Kong (1); Chang H. Lee (1); Ling He (1,3); Lusai Xiang (1,3); Jeffrey A. Ahn (1); Shen Ding (4); & Jeremy J. Mao (1,2,3)

(1) Center for Craniofacial Regeneration, Columbia University Medical Center, 630 W. 168 St.-PH7E, New York, NY 10032, USA
(2) Department of Biomedical Engineering, Columbia University, 500 W. 120th St., Mudd 510, New York, NY 10027, USA
(3) Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-sen University, 56 Lingyuanxi Road, Guangzhou 510055, China
(4) Gladstone Institute of Cardiovascular Disease, Department of Pharmaceutical Chemistry, University of California San Francisco, 505 Parnassus Ave, San Francisco, CA 94122, USA

Filed Under: New Publications Tagged With: PPAR, PPARγ

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