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The identification of appropriate cell types is necessary to establish cell-based therapies in regenerative medicine. These cell types must (1) be available in an appropriate amount, (2) be easy to obtain, (3) be sufficiently expandable in vitro, and (4) fit to or at least be able to differentiate into the required cell type. Since the umbilical cord is available without any intervention and represents a notable amount of tissue, we consider it to be a promising source for isolating cells for cell-based therapies. This study demonstrates that umbilical cord stromal cells (UCSC), the connective tissue cells of the umbilical cord, can be isolated in sufficient quantities and be well expanded. UCSC feature phenotypic plasticity and thus are functionally similar to stem cells. UCSC can be differentiated into cells with osteoblastic properties (expression of alkaline phosphatase, formation of bone nodules). It is concluded that the umbilical cord should no longer be regarded as valueless tissue and be unthinkingly discarded. Instead, it should be considered a valuable resource for the isolation of potent cells for cell-based therapies, especially for treatment of bone defects.

Turmeric, a product of Curcuma longa, has a very long history of being used for the treatment of wounds in many Asian countries. Curcumin, the principal curcuminoid of turmeric, has recently been identified as a main mediator of turmeric’s medicinal properties. However, the inherent limitations of the compound itself, such as hydrophobicity, instability, poor absorption and rapid systemic elimination, pose big hurdles for translation to wider clinical application. We present here an approach for engineering curcumin/gelatin-blended nanofibrous mats (NMs) by electrospinning to adequately enhance the bioavailability of the hydrophobic curcumin for wound repair. Curcumin was successfully formulated as an amorphous nanosolid dispersion and favorably released from gelatin-based biomimetic NMs that could be easily applied topically to experimental wounds. We show synergistic signaling by the released curcumin during the healing process: (i) mobilization of wound site fibroblasts by activating the Wnt signaling pathway, partly mediated through Dickkopf-related protein-1, and (ii) persistent inhibition of the inflammatory response through decreased expression of monocyte chemoattractant protein-1 by fibroblasts. With a combination of these effects, the curcumin/gelatin-blended NMs enhanced the regenerative process in a rat model of acute wounds, providing a method for translating this ancient medicine for use in modern wound therapy. Loading an ancient medicine onto gelatin nanofibres enhances the production of wound-healing and anti-inflammatory agents in rat models. Turmeric, the main spice in curry powder, has been used to clean and manage injuries for thousands of years. Recent studies have identified curcumin as the responsible compound for many of its medicinal properties. Now, Xinyi Dai and Arndt Schilling from Germany's Technical University of Munich and University Medical Center Gottingen and colleagues have improved curcumin's bioavailability by electrospinning it with gelatin into a tissue-mimicking network of cross-linked nanofibres. X-ray measurements showed that this procedure turned normally crystalline curcumin into an amorphous dispersion with good solubility in cellular environments. Trials on rat skins revealed that the amorphous curcumin boosted the metabolism of beneficial fibroblast cells and helped regulate anti-inflammation proteins for significantly faster wound healing. Schematic illustration of nanoformulated curcumin accelerates wound healing. (a) Curcumin nanoformulation through electrospinning greatly enhances its solubility. (b) Topically applied Curcumin/Gelatin nanofibrous mat releases bioactive curcumin to mobilize wound site fibroblasts by enhancing both cell proliferation and migration, a process partially mediated by Dickkopf-related protein-1-regulated Wnt/β-catenin pathway signaling. In the mean time, fibroblasts decreased the expression of monocyte chemoattractant protein-1, leading to lasting inhibition of inflammatory response during the healing process. As a result, wound environment turns out to be more in favor of physiological healing, with faster re-epithelialization, granulation tissue formation, as well as collagen deposition and matuaration from proliferative fibroblasts.