Robert M Lavker

  • 13281 Citations
1969 …2023
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Personal profile

Research Interests

My laboratory focuses on defining how self-renewing epithelia (e.g., epidermis, corneal and conjunctival epithelia, hair follicle) maintains homeostasis. Such steady-state systems are, by definition, governed by stem cells and we have pioneered investigations on the biological properties of epithelial stem cells. In collaboration with Tung-tien Sun (NYU) our lab was the first to propose the concept of epithelial basal cell heterogeneity and to demonstrate that a subpopulation of epidermal basal cells were putative stem cells. In collaboration with George Cotsarelis (UPENN), we demonstrated that the stem cells of the corneal epithelium were preferentially localized as a subset of limbal epithelial basal cells. This observation has had vast translational impact on vision, as it altered the manner by which corneal epithelial transplant surgery was conducted and formed the foundation for ex vivo expansion of limbal stem cells for use in conditions of limbal stem cell deficiency. Our laboratory was also the first to localize the hair follicle epithelial stem cells to the bulge region of the outer root sheath. This observation helped explain, in part, the mechanisms underlying the hair growth cycle. We were also the first to formally demonstrate that the hair follicle stem cells were bi-potent, capable of giving rise to not only the cells that formed the hair shaft, but also to the epidermis. This finding was important for our understanding of how the hair follicle provided proliferative cells to the epidermis during times of tissue expansion and wound repair. With respect to how the stem cells are regulated, my laboratory was the first to evaluate the expression profile and localization of microRNAs, which are part of the RNA silencing machinery in corneal and lens epithelia and retinal tissues. We identified miR-184 as a corneal-preferred miRNA that is angiostatic and maintains corneal avascularity. We found that miR-31, another corneal-preferred miRNA, positively regulated Notch signaling via a novel hydroxylase to insure proper corneal epithelial and epidermal differentiation. Most recently, my laboratory has demonstrated that the miR-103/107 family is vital in maintaining limbal epithelial stem cell homeostasis as well as insuring proper end stage autophagy.

Dr. Lavker is the Jack W. Graffin, M.D. Professor of Dermatology and Director of Research in the department. H has spent the last 50 years studying various aspects of cutaneous biology and published over 150 original scientific papers. In addition to his research endeavors, he has considerable administrative abilities. Prior to joining Northwestern University, Dr. Lavker was a member of the faculty of the University of Pennsylvania for 26 years. He served as Principal Investigator on the University of Pennsylvania’s Department of Dermatology Training Grant from 1987-2001. He has had continuous NIH funding since 1982 and is currently the Principal Investigator on 2 NIH R01 grants and a T-32 Training Grant in Cutaneous Biology. Dr. Lavker has played an important role in the research training of individuals within the departments of dermatology at the University of Pennsylvania and Northwestern University. In addition to his scientific and teaching responsibilities, he holds and has held numerous leadership positions. He served as Associate Chairman of the Department of Dermatology at the University of Pennsylvania and administered all aspects of research from 1993-1994. He also served on the Executive Committee, the Resident Selection Committee, and the Appointments and Promotions Committee of the Department of Dermatology at both Northwestern University and the University of Pennsylvania. Dr. Lavker was Chair of the NU Medical School’s Committee on Appointments and Promotions (APT) from 2007-2009 and continue to Chair the department’s APT committee. He was a member of the Research Council at Northwestern University, which managed all research-related activities on campus and evaluated all of the medical school’s core facilities. Dr. Lavker served on the Board of Directors of the Society for Investigative Dermatology from 1997-2000, and was an Associate Editor of the Journal of Investigative Dermatology from 2002-2014.

Training Experience

1969Postdoctoral Fellowship, Boston University

Education/Academic qualification

PhD, Clemson University

… → 1968

Research interests

  • Cell Biology
  • Cutaneous Biology
  • Gene Regulation
  • Hair
  • Ophthalmology
  • Skin Cancer
  • Stem Cells

Fingerprint Dive into the research topics where Robert M Lavker is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 9 Similar Profiles
Skin Medicine & Life Sciences
Keratinocytes Medicine & Life Sciences
Stem Cells Medicine & Life Sciences
Epidermis Medicine & Life Sciences
Epithelial Cells Medicine & Life Sciences
Hair Follicle Medicine & Life Sciences
Corneal Epithelium Medicine & Life Sciences
Epithelium Medicine & Life Sciences

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Grants 2002 2023

MicroRNAs
Homeostasis
Corneal Epithelium
HDL Lipoproteins
Nanoparticles
Mentors
Dermatology
Skin
Research
Allergy and Immunology
Corneal Epithelium
Autophagy
Epithelial Cells
EphA2 Receptor
Homeostasis
Imaging techniques
Microscopic examination
Microscopes
Medicine
Robotic arms

Research Output 1969 2018

2 Citations (Scopus)

Emerging therapeutic strategies for limbal stem cell deficiency

Dong, Y., Peng, H. & Lavker, R. M., Jan 1 2018, In : Journal of Ophthalmology. 2018, 7894647.

Research output: Contribution to journalReview article

Stem Cells
Epithelial Cells
Therapeutics
Corneal Epithelium
Corneal Neovascularization
4 Citations (Scopus)

Epha2/ephrin-A1 mediate corneal epithelial cell compartmentalization via ADAM10 regulation of EGFR signaling

Kaplan, N., Ventrella, R., Peng, H., Pal-Ghosh, S., Arvanitis, C., Rappoport, J. Z., Mitchell, B. J., Stepp, M. A., Lavker, R. M. & Getsios, S., Jan 1 2018, In : Investigative Ophthalmology and Visual Science. 59, 1, p. 393-406 14 p.

Research output: Contribution to journalArticle

Ephrin-A1
Epidermal Growth Factor Receptor
Epithelial Cells
Corneal Epithelium
EphA2 Receptor
1 Citation (Scopus)

EphA2 Transmembrane Domain Is Uniquely Required for Keratinocyte Migration by Regulating Ephrin-A1 Levels

Ventrella, R., Kaplan, N., Hoover, P., Perez-White, B. E., Lavker, R. M. & Getsios, S., Oct 1 2018, In : Journal of Investigative Dermatology. 138, 10, p. 2133-2143 11 p.

Research output: Contribution to journalArticle

Ephrin-A1
Keratinocytes
Ligands
Membranes
EphA2 Receptor
1 Citation (Scopus)

Autophagy and macropinocytosis: Keeping an eye on the corneal/limbal epithelia

Peng, H., Park, J. K. & Lavker, R. M., Jan 1 2017, In : Investigative Ophthalmology and Visual Science. 58, 1, p. 416-423 8 p.

Research output: Contribution to journalArticle

Corneal Epithelium
Autophagy
Homeostasis
Epithelium
4 Citations (Scopus)

Crosstalk between signaling pathways in pemphigus: A role for endoplasmic reticulum stress in p38 Mitogen-activated protein kinase activation?

Cipolla, G. A., Park, J. K., Lavker, R. M. & Petzl-Erler, M. L., Sep 5 2017, In : Frontiers in immunology. 8, SEP, 1022.

Research output: Contribution to journalArticle

Endoplasmic Reticulum Stress
Pemphigus
p38 Mitogen-Activated Protein Kinases
Keratinocytes
Acantholysis