The Crisa Laboratory

Our group is interested in three complementary research areas: 1) Understand the biologic role of bone marrow-derived vasculogenic cells in tissue repair and transplant engraftment; 2) Identify developmental cues provided by myeloid immune cells to pancreatic progenitors and exploit these cues for pancreatic islet cell regeneration; 3) Engineer islet-like tissue microenvironments to enhance transplant engraftment in vivo, and to model diabetogenic insults and therapies ex-vivo.

Understanding the biologic role of bone marrow-derived vasculogenic cells in tissue repair and transplant engraftment.
Because of its strategic positioning at the interface between the graft and circulating immune cells, the biological characteristics of the endothelium forming new blood vessels during tissue repair are of primary importance to the survival of transplants. We have identified a subset of human cord blood-derived hemopoietic progenitors that exhibits the developmental potential and functional properties of true endothelial progenitor cells through engagement of angiopoietin-dependent signals. Using animal models, we have further defined unique developmental, phenotypic and functional characteristics of bone-marrow-derived versus tissue-derived endothelial cells in islet transplant settings. Currently, this line of research aims to define the survival/proliferative/ differentiative signals delivered by bone marrow-derived vascular cells to islet tissue, and their involvement in modifying innate immune responses during tissue repair. Understanding these issues may lead to new strategies to improve islet transplant engraftment and ensure immune protection of the grafts.

Identify developmental cues provided by myeloid immune cells to pancreatic progenitors and exploit these cues for pancreatic islet cell regeneration.
Tissue macrophages populate the mesenchymal compartment of all organs during embryogenesis and have been shown to support tissue organogenesis and regeneration. Nevertheless, the current dogma in the field is that their function(s) is peripheral to cell-autonomous epithelial development, i.e. being mainly restricted to clearance of apoptotic cells and remodeling of the extracellular matrices. By using organ culture and in vivo models, we found instead that macrophages in select states of activation directly influence the transcriptional program of pancreatic epithelial progenitors. Using myeloid cell subset-specific depletion models, we further discovered that myeloid cells marked by the expression of CCR2 are critically required for the establishment of the islet cell mass in perinatal life and islet regeneration in adulthood after injury. Gene profiling of these myeloid cell populations has pointed to candidate pro-regenerative pathways currently under investigation.

Engineer islet-like tissue microenvironments to enhance transplant engraftment in vivo, and to model diabetogenic insults and therapies ex-vivo.
Since her appointment at the University of Washington, together with other members of the DOCE and ISCRM, Dr. Crisa has been engaged in efforts to develop a Diabetes Stem Cell Program, also part of the Institute of Stem Cell and Regenerative Medicine. Over the past years, our team has generated several pluripotent stem cell lines from different genetic backgrounds, and distinct cell types, and is now investigating unique signature pathways that dictate their ability to engraft in immune competent hosts, with a primary focus on those involved in the recruitment of vasculogenic cells and/or in the modulation of immunoregulatory networks. More recently, in collaboration with bioengineers, we have designed in vitro organ model systems that, thanks to biochemical patterning and microfluidic technologies, can emulate in vivo-like tissue microenvironments. Our medium and long-term plan is to further develop these model systems to mimic key aspects of pancreatic islet physiology and pathology, as well as to exploit these systems as a drug-screening platform to assess efficacy and safety of therapeutics.