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http://dspace.mediu.edu.my:8181/xmlui/handle/1957/5992| Title: | Determining cytokine induced vascular maturity through immunohistochemical double-staining |
| Authors: | Peattie, Robert McGuire, Joe Barbar, Elisar Kruzic, Jamie |
| Keywords: | angiogenesis growth factors cytokines hyaluronic acid immunohistochemistry microvessels capillaries maturation |
| Issue Date: | 16-Oct-2013 |
| Description: | Graduation date: 2008 As a major natural component of the extracellular matrix (ECM), hyaluronic acid (HA) is an excellent choice for biomimetic, biocompatible therapeutic materials. Furthermore, thiol-modified forms of HA are capable of forming macroporous hydrogels that allow for both controlled cytokine release and extensive vessel in-growth. It has previously been shown that this HA controlled cytokine release may be extended significantly by including thiol-modified heparin (Hp) in the hydrogel matrix. We therefore hypothesized that that the inclusion of minute quantities of Hp in both HA and HA+Gelatin cytokine-loaded hydrogels would, in turn, result in extended levels of elicited microvascular stability and maturity in vivo. To test this hypothesis we formulated several single and dual cytokine-loaded hydrogels and implanted them into the Balb/c mouse ear pinna. These preloaded hydrogels contained vascular endothelial growth factor (VEGF), angiopoietin-1 (Ang-1), keratinocyte growth factor (KGF) or platelet derived growth factor (PDGF) either individually or in combination with VEGF. At 7 and 14 days post surgery, elicited vascular maturity levels were quantified using immunohistochemical (IHC) staining techniques. The degree of circumferential pericyte ensheathement as indicated by alpha smooth muscle actin (α-SMA) IHC signal, together with basement membrane morphology, allowed for a graded determination of elicited microvasculature maturity. The progress of maturation was separated from the natural wound response (sham surgery) and then normalized to the steady state (contralateral ear), and reported as a vascular maturity index (VMI). It was discovered that in both gel types at both time points, the dual cytokine combination elicited greater maturity levels than either cytokine administered individually. For example, VEGF and KGF-containing implants at day 7 yielded VMI values of -0.1375 and -0.092, respectively, whereas their combination resulted in a VMI of 0.176 (p < 0.007). At day 7, only one of the seven HA:Hp experimental cases yielded a positive VMI (VEGF+KGF), whereas four of the seven HA:Hp cases yielded positive VMI values at day 14. This shift from predominantly negative to predominantly positive VMI values suggested not only a sustained microvascular maturity response, but also a gradual improvement in microvessel maturity relative to the sham tissue. Although sustained, and in some cases elevated from 7 to 14 days post film implantation, the microvascular maturity response elicited by HA:Hp films was not invariably higher than that elicited by the HA controls. The levels of elicited microvascular maturity in tissue treated with dual cytokine loaded HA:Hp films were instead found to depend on the identity of the late stage cytokine, suggesting specific heparin-cytokine interactions were responsible for the observed differences. |
| URI: | http://koha.mediu.edu.my:8181/xmlui/handle/1957/5992 |
| Other Identifiers: | http://hdl.handle.net/1957/5992 |
| Appears in Collections: | ScholarsArchive@OSU |
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