Julie Sneddon, PhD

Asst Professor
Diabetes Center
+1 415 502-3380
Research Overview: 

The primary focus of our laboratory is pancreatic development and Type I Diabetes, and we employ the tools of stem cell biology, developmental biology, genomics, and tissue engineering.

One key goal of regenerative biology is the generation of functional cells to replace those missing or lost in disease. These cells of defined function, however, such as insulin-producing pancreatic beta cells, exist in animals only as part of a larger organ composed of a complex and incompletely defined mixture of cells. The interactions among the cells in this mixture are critical for the function of the individual cell types. For example, beta cells isolated from the pancreas and transferred to culture rapidly lose their ability to release insulin in response to glucose. Furthermore, widespread ablation of non-epithelial cells in the pancreas significantly compromises beta cell production and function. Thus far, however, the identities and specific functions of these non-epithelial cell types remain largely unknown.

In our laboratory, we aim to understand the underlying biology of the cellular microenvironment, including the cellular diversity and lineage relationships of the non-epithelial compartment of the pancreas in the context of organogenesis, adult organ function, and disease. A deeper understanding of the identity and biology of non-epithelial cell types within the pancreas and other organs will enable a more directed and efficient attempt at replacing lost cell and organ function via regenerative medicine.

Primary Thematic Area: 
Developmental & Stem Cell Biology
Secondary Thematic Area: 
Tissue / Organ Biology & Endocrinology
Research Summary: 
Pancreas development, disease, and regeneration
Mentorship Development: 

12/19/19    ACRA: Setting Training Expectations for Trainees on the Academic Career Track (1.5 hours)
3/3/20    Promoting Student Mental Health:A Presentation and Discussion (Staff and Faculty)
3/3/20    Promoting Student Mental Health: Faculty Workshop (Faculty only)
6/10/20    Tools and Tips for Virtual Learning
11/10/20    Optimizing the Efficiency of Your Lab
5/25/21  Sharpening your Mentoring Skills (SyMS) 

Websites

Publications: 

Replenishable prevascularized cell encapsulation devices increase graft survival and function in the subcutaneous space.

Bioengineering & translational medicine

Chendke GS, Kharbikar BN, Ashe S, Faleo G, Sneddon JB, Tang Q, Hebrok M, Desai TA

Rab11 is essential to pancreas morphogenesis, lumen formation and endocrine mass.

Developmental biology

Barlow HR, Ahuja N, Bierschenk T, Htike Y, Fassetta L, Azizoglu DB, Flores J, Gao N, De la O S, Sneddon JB, Marciano DK, Cleaver O

Loss of Fgf9 in mice leads to pancreatic hypoplasia and asplenia.

iScience

Patzek S, Liu Z, de la O S, Chang S, Byrnes LE, Zhang X, Ornitz DM, Sneddon JB

Doxycycline Significantly Enhances Induction of iPSCs to Endoderm by Enhancing survival via AKT Phosphorylation.

Hepatology (Baltimore, Md.)

Peaslee C, Esteva-Font C, Su T, Munoz-Howell A, Duwaerts C, Liu Z, Rao S, Liu K, Medina M, Sneddon JB, Maher JJ, Mattis AN