Journal of Cardiology & Cardiovascular Therapy

Research Article

Dehydrated Human Amnion/Chorion Membrane Allograft Promotes Cardiac Repair Following Myocardial Infarctions

Jeremy J Lim¹, James Fonger² and *Thomas J Koob¹

¹MiMedx Group Inc., Georgia

²Innovation Perspectives, Georgia

Submission: December 22, 2016; Published: January 10, 2017

*Corresponding author: Thomas J Koob, PhD, 1775 West Oak Common Court NE, Marietta, GA 30062, Georgia, Tel:(770)651-6115; Fax:(770)590-3562; Email:tkoob@mimedx.com

How to cite this article: Jeremy J L, James F, Thomas J K. Dehydrated Human Amnion/Chorion Membrane Allograft Promotes Cardiac Repair FollowingMyocardial Infarction. J Cardiol & Cardiovasc Ther 2017; 2(5): 555599. DOI: 10.19080/JOCCT.2017.02.555599

Abstract

There is a rising need for novel therapies for the treatment of acute myocardial infarction (MI). Dehydrated human amnion/chorion membrane (dHACM) contains a unique array of regenerative cytokines and growth factors, involved in the regulation of tissue healing and modulation of inflammation; therefore, the ability of dHACM to prevent cardiac damage or promote healing in an in vivo mouse model of acute myocardial infarction was investigated. Acute left ventricular MI was induced in mice by coronary artery ligation. dHACM patches were then sutured to the MI zones, or the infarcted hearts were injected with saline as a control.

After eight weeks post-treatment, dHACM-treated and saline-treated hearts were histological sectioned and stained with Masson’s trichrome to quantify infarct size or with antibodies for c-Kit for recruitment of c-Kit positive stem/progenitor cells, Ki67 for proliferation, TUNEL staining for apoptosis, and CD31 for vascular endothelial cells. Results indicated that dHACM grafts promoted cardiac repair in vivo after MI by reducing the size of fibrotic scarring. An examination of cellular activity demonstrated an increased number of c-Kit positive cells, greater cell proliferation with inhibition of apoptosis, and an increased number of CD31 positive vessels in dHACM-treated cardiac tissue. These results show that treatment with dHACM in this animal model improved cardiac repair following MI through multiple paracrine effects, including through improved blood supply and recruitment of autologous stem cells.

Keywords: dHACM; Amnion; Chorion; Amniotic Membrane; Myocardial Infarction; Stem Cell

Abbreviations: MI: Myocardial Infarction; PPCI: Primary Percutaneous Coronary Intervention; LV: Left Ventricular; LVAD: Left Ventricular Assist Device; dHACM: dehydrated Human Amnion/Chorion Membrane; FDA: Food and Drug Administration; AATB: American Association of Tissue Banks; HIV: Human iImmunodeficiency Virus; HTLV: Human T-Lymphotropic Virus; IACUC: Institutional Animal Care and Use Committee; NOD: Non-Obese Diabetic; SCID: Severe Combined Immuno-Deficiency; LAD: Left Anterior Descending; TUNEL: Terminal deoxynucleotidyl transferased UTP Nick End Labeling; ANOVA: Analysis of Variance; SCF: Stem Cell Factor

Introduction

Acute myocardial infarction (MI), more commonly known as heart attack is a major consequence of cardiovascular disease and a leading cause of morbidity and mortality worldwide. Acute MI occurs when coronary occlusion causes diminished blood supply to the cardiac tissue, and myocardial ischemia results in irreversible damage or cell death [1]. Reperfusion therapy in the form of primary Percutaneous coronary intervention (PPCI) has become the gold standard of treatment for MI and has significantly improved short-term outcomes; however, damage to the cardiac tissue still results in post-MI left ventricular (LV) remodeling. LV remodeling occurs in response to loss of myocardial function in the form of tissue scarring, dilatation, and hypertrophy, and while remodeling is initially beneficial, this compensatory mechanism can be maladaptive, ultimately leading to heart failure [2]. There are currently about 5.1 million Americans living with heart failure with 825,000 new cases each year. It is estimated that the total direct and indirect costs for heart failure in the United States exceed $30 billion each year [3].

Therefore, there is a rising and urgent need for novel therapies for the treatment of MI, particularly to treat or prevent post-MI LV remodeling. Currently, pharmacologic, LV assist devices (LVADs), and total heart transplantation are the only forms of treatment, and none of them are without significant limitations. For example, the efficacy of pharmacologic for the prevention and treatment of post-MI LV remodeling and heart failure is limited, LVADs are mainly used as a temporary bridge to cardiac transplantation, and cardiac transplantation faces limited donor availability and is only used as a last course of action. Due to the inability of cardiac muscle to regenerate following injury, stem cell therapy has been widely explored as a treatment for cardiac disease, including numerous ongoing clinical trials; however, significant gains in cardiac function have yet to be established [4-6]. Poor engraftment and low survival rates of injected cells represent major limiting factors in the efficacy of cellular therapies for cardiac repair [4-7].

Dehydrated human amnion/chorion membrane (dHACM) patches (EpiFix® and AmnioFix®, MiMedx Group, Marietta, GA) are human allografts comprised of laminated amnion and chorion amniotic membranes derived from the placenta. By using a gentle cleansing and dehydration process (PURION® Process), dHACM retains and preserves the native extracellular matrix architecture and biological activity of the amniotic membrane tissue [8-10]. The properties of PURION Processed dHACM suggest that it may be a promising tissue for use in treatment of acute MI. dHACM contains structural collagen and additional extracellular matrix proteins, as well as a unique array of regenerative cytokines and growth factors, involved in the regulation of wound healing and inflammation [11-14]. These soluble cues remain biologically active in dHACM and have been shown to promote cell proliferation and endogenous growth factor production, recruit stem and progenitor cells, and promote angiogenesis [11-17]. Amniotic membranes are also known to be immunologically privileged tissues with the ability to reduce pain, prevent scarring, and control inflammation [18,19]. Recent clinical trials have established the ability of dHACM to promote healing in a variety of refractory wounds without recurrence in long-term follow-up [20-22], while preliminary results suggest that dHACM may also play a protective role in preventing the progression of osteoarthritis [23]. These properties suggest that dHACM may also possess the ability to either prevent damage or assist cardiac repair following MI.

As a proof-of-concept evaluation, the ability of dHACM to attenuate damage or promote cardiac repairin a mouse model of acute myocardial infarction was investigated, including effects on infarct size and cardiac remodeling. dHACM was examined for its ability to reduce scar formation and inflammation, promote cell proliferation and survival, attract endogenous stem/progenitor cells, and enhance angiogenesis in vivo.

Material and Methods

Dehydrated Human Amnion/Chorion Membrane (dHACM)

dHACM is a dehydrated human allograft comprised of laminated amnion and chorion membranes derived from the placenta [8-10]. Human placentas were donated under informed consent, following Caesarean sections, in compliance with the Food and Drug Administration’s (FDA) Good Tissue Practice and American Association of Tissue Banks (AATB) standards. All donors were tested and confirmed to be free of infectious diseases, including human immunodeficiency virus (HIV), human T-lymph tropic virus (HTLV), hepatitis B and C, and syphilis. Amnion and chorion were isolated from placenta and processed with a proprietary PURION® Process that involves gentle cleansing of the layers. The amnion and chorion were then laminated to form the graft, and the graft was dehydrated under controlled drying conditions [10]. Specific versions of dHACM (EpiFix® and AmnioFix®, MiMedx Group) were used as the test material in these studies; therefore, the results of these studies apply only to PURION® Processed dehydrated human amnion/chorion composite grafts (dHACM).

Myocardial Infarct (MI) Model

A previously established mouse myocardial infarction model was used to examine the efficacy of dHACM in inducing cardiac repair [24-27]. All marine experiments were conducted in accordance with protocols approved by the University of Miami’s Institutional Animal Care and Use Committee (IACUC). Either 8-week old female non-obese diabetic (NOD)/severe combined immunodeficiency (SCID) mice or wild type mice, obtained from the Jackson Laboratory (Bar Harbor, ME),were used to examine the effects of human amniotic membrane implants in a mouse xenograft model. Mice were anesthetized, orally intubated, and underwent left thoracotomy in the fourth intercostals space. The left anterior descending branch of the coronary artery (LAD) was legated using an 8-0 nylon suture to induce MI.

dHACM Treatment

Following acute myocardial infarction, mice were either treated with a dHACM patch or with saline control treatment. 5 mm x 5 mm dHACM patches (EpiFix® or AmnioFix®) were sutured to the MI zones. Mice receiving saline injections alone were used as controls. The pericardium was re-draped over the heart, and the chest was closed. Animals were placed into clean cages and housed for the duration of 8weeks after recovery. n=10 mice were used for treatment and control groups, and the investigators were blinded to the type of treatment. Mice that did not recover from the coronary artery ligation due to surgical mortality were excluded from analysis. Animal deaths did not appear to be related to dHACM treatment.

Histological Staining of Infarcts

Eight weeks post-treatment, mice were euthanized, and analyzed for cardiac remodeling. Hearts from each group were fixed in 10% formalin, and embedded in paraffin. Paraffin sections were subjected to Masson’s Trichrome staining, and quantization of infarct size was performed. The average infarct size was obtained by calculation of the average length of the circumference in the infarct portion and the normal area. These indices of cardiac remodeling were compared among dHACM treatment groups and saline controls.

Immunohistochemistry

To study if dHACM contributes paracrine factors that resulted in enhanced cardiomyocyte proliferation, decreased apoptosis, and induce recruitment of local c-Kit positive cardiac progenitor cells or endogenous stem cells into the infarcted area, tissue sections were stained with antibodies specific for Ki67 (proliferation marker), terminal deoxynucleotidyl transferase dUTP nick end labeling (TUNEL) for apoptosis, and c-Kit, respectively.

To examine vascularization in cardiac tissue, histological tissue sections were also stained with antibodies for CD31 to identify vascular endothelial cells. The sections were counterstained for troponin (red) for myocardial tissue and with DAPI (blue) for cell nuclei. The total number of CD31- positivevessels per 1.0x104 μm2 of MI area was counted and compared in samples across different groups, as a measure of vascularity.

Statistical Analysis

Values were reported as mean ± standard deviation. Statistical analyses were performed using analysis of variance (ANOVA) with Tukey’s post hoc test for pair wise comparisons. Significant differences were assigned when p≤0.05.

Results

dHACM treatment reduced infarct size following MI

A collagenous scar was visible in the infarct sites, indicating that coronary artery ligation resulted in cardiac fibrosis (Figure1), blue. dHACM treated mice showed a significant decrease of approximately 50% in infarct area following MI, compared to control (saline) treated mice p≤0.05; (Figure 1). There was no statistically significant difference in infarct size between the EpiFix and AmnioFix-treated mice; therefore, all dHACM patch results were combined for the following analyses. Additionally, reduction in infarct size was seen in both dHACM-treated NOD/ SCID and wild type mice, indicating that the dHACM tissue was well tolerated by wild type mice.

dHACM treatment recruited c-Kit positive stem cells following MI

A significant increase in the stem cell marker c-Kit was observed in dHACM-treated hearts, compared to the control group p≤0.05; (Figure 2). Significantly greater numbers of c-Kit positive cells were present both in the region directly in contact with the dHACM, as well as regions of the heart peripheral to the membranes. c-Kit is a cell surface receptor for stem cell factor (SCF), and it is a marker for hematopoietic stem cells and cardiac stem/progenitor cells [28,29]. Therefore, the increased presence of c-Kit positive cells indicated that dHACM treatment promoted the recruitment of endogenous c-Kit-positive stem cells either from the bone marrow or locally from the heart to the site of infarction following acute MI.

dHACM treatment promoted cardiomyocyte survival following MI

There was a significant increase in the cell proliferation marker Ki-67 in the membrane-treated hearts, compared to the control group p≤0.001; (Figure 3). Ki-67 expression also extended beyond the region in direct contact with the membranes into the distal heart tissue. Ki-67 is a nuclear protein that is a marker for proliferating cells [30]. Additionally, there was a significant decrease in apoptosis in the membranetreated hearts, compared to the saline treatment (p≤0.001), as measured by TUNEL staining (Figure 4). TUNEL staining is indicative of DNA fragmentation, correlated to cell apoptosis. Increased Ki-67/troponin double-positive cells and decreased TUNEL/troponin double positive cells indicated that dHACM treatment promoted cardiomyocyte proliferation and inhibited cardiomyocyte apoptosis, concurrently. These data suggest that paracrine signals from the dHACM patches promoted cell proliferation, inhibited apoptosis, and enhanced cell survival following MI.

dHACM treatment promoted angiogenesis following MI

An increased number of blood vessels were found in the membrane-treated hearts, compared to the control mice (p≤0.05), as indicated by staining for CD31 positive vessels (Figure 5). CD31 is a cell surface marker for vascular endothelial cells. An increase in CD31 positive vessels indicated enhanced vascularization in the cardiac tissue, suggesting that dHACM treatment increased angiogenesis and neovascularization within the cardiac tissue following MI.

Discussion

Using an established coronary artery ligation model of acute left ventricular myocardial infarction, these results represent proof-of-concept that treatment with dehydrated human amnion/chorion membrane (dHACM) grafts maybe capable of promoting cardiac repair in vivo after MI. dHACM treatment reduced the size of fibrotic scarring after MI, indicating that dHACM had a protective effect on the ischemic tissue. Fibrosis of cardiac tissue is an important aspect of cardiac remodeling, as the collagenous scar remains stiff and unable to contract. Cardiac scar tissue leads to further remodeling, including left ventricular hypertrophy, a compensatory mechanism which can ultimately result in heart failure.

As an initial investigation to determine the mechanism of action for dHACM-mediated cardiac repair, an examination of cellular composition and activity in the cardiac tissue was performed to examine a number of events which may promote cardiac repair. An increased number of c-Kit positive cells were identified in dHACM-treated cardiac tissue, suggesting the dHACM may recruit c-Kit positive hematopoietic stem cells and/or cardiac stem cells to the site of injury, stimulating repair. Additionally, dHACM promoted cell proliferation while inhibiting apoptosis, as demonstrated by Ki-67 and TUNEL staining, respectively, demonstrating enhanced cell survival. Finally dHACM treatment resulted in an increased number of CD31 positive vessels in cardiac tissue after MI, indicative of enhanced angiogenesis. Together these results suggest that treatment with dHACMmay improve cardiac repair following MI through multiple paracrine effects. dHACM protected cardiac cells and tissue from damage in vivo, possibly through improved blood supply to the infarcted tissue. Additionally, dHACM recruited autologous stem/progenitor cells into the ischemic cardiac tissue. Recruitment of autologous cardiac stem cells possesses tremendous potential to promote repair and regeneration of cardiac tissue.

The properties of dHACM suggest that it may be a potential therapeutic biomaterial for MI treatment as a cardiac patch. dHACM contains a vast array of growth factors and cytokines within a naturally-derived extracellular matrix scaffold. The PURION Process preserves the bioactivity inherent to amniotic membrane tissue, including a unique array of regenerative cytokines and growth factors. To date, over 226 growth factors, cytokines, and regulatory molecules have been identified in dHACM tissues [11-14,31]. These soluble cues remain biologically active in dHACM, combining to promote cell proliferation and endogenous growth factor production of various cell types, recruit stem cells to the site of implantation, and promote angiogenesis in vitro and in vivo [11-17]. dHACM is also inherently biocompatible and non immunogenic. Amniotic membrane is an immunologically privileged tissue that acts as a natural barrier between the mother and developing fetus, and treatment with amniotic tissue has demonstrated the ability to reduce pain, prevent scarring, and modulate inflammation [18,19]. Therefore, dHACM tissue represents a structural patch that contains collagen and extracellular matrix which may also serve as a biologically active bandage for the infarct zone.

This is the first report that dHACM has positive effects in protecting tissue or promoting repair following acute myocardial infarction. A previous study by Cargnoni et al. [32] demonstrated that fresh human amniotic membrane (used within 24 hours) significantly reduced post-ischemic cardiac injury using a similar rat coronary artery ligation model [32]. In the Cargnoni study, amniotic membrane-treated rats demonstrated preservation of cardiac dimensions and improved cardiac contractile function, in terms of higher left ventricle ejection fraction, fractional shortening, and wall thickening, within 7 days after application and persisting for at least 2 months [32]. Additionally, no engraftment of amniotic cells was detected into host cardiac tissues, suggesting that repair was likely mediated by the release of cardio protective soluble factors to the injured ischemic tissue [32]. Since dHACM used in this study is dehydrated and does not contain viable cells but retains and preserves the bioactive cellular components of the native amniotic membrane, it is likely that the cardiac repair demonstrated here is also mediated through similar soluble signals.

These results suggest that dHACM may warrant further investigation for use in cardiac repair following myocardial infarction. Follow up studies will include demonstrating improvement of important functional outcomes such as left ventricular dimensions, contractility, and ejection volume, as well as demonstrating efficacy in a large animal model of MI, such as a porcine model. Additional experiments are also required to further elucidate the roles of stem cell recruitment and neovascularization in cardiac repair, including potential interactions and characterization of the molecular mechanisms underlying the efficacy of dHACM in the repair of other tissues. However, this work is a first step suggesting that dHACM allografts possess tremendous potential in promoting cardiac repair following acute myocardial infarction.

Conclusion

dHACM allografts appeared to promote cardiac repair after MI by reducing the size of fibrotic scarring in a mouse model. Application of dHACM patches stimulated an increase in c-Kit positive stem cells, cell survival, and vascularization in infarcted cardiac tissue. These results suggest that treatment with dHACM following MI may improve cardiac repair through multiple paracrine effects, including through improved blood supply and recruitment of autologous stem cells.