Phased ERK responsiveness and developmental robustness regulate teleost skin morphogenesis

N Nitya Ramkumar (Department of Cell Biology, Duke University Medical Center) C Christian Richardson (Department of Cell Biology, Duke University Medical Center) M Makinnon O'Brien (Department of Cell Biology, Duke University Medical Center) F Faraz Ahmed Butt (Department of Cell Biology, Duke University Medical Center) J Jieun Park A Anna T. Chao (Department of Cell Biology, Duke University Medical Center) M Michel Bagnat (Department of Cell Biology, Duke University Medical Center) K Kenneth D. Poss S Stefano Di Talia

Abstract

Elongation of the vertebrate embryonic axis necessitates rapid expansion of the epidermis to accommodate the growth of underlying tissues. Here, we generated a toolkit to visualize and quantify signaling in entire cell populations of the periderm, the outermost layer of the epidermis, in live developing zebrafish. We find that oriented cell divisions facilitate growth of the early periderm during axial elongation rather than cell addition from the basal layer. Activity levels of Extracellular signal-regulated kinase (ERK), a downstream effector of the MAPK pathway, gauged by a live biosensor, predict cell cycle entry, and optogenetic ERK activation regulates cell cycling dynamics. As development proceeds, rates of peridermal cell proliferation decrease, and ERK activity becomes more pulsatile and functionally transitions to promote hypertrophic cell growth. Targeted genetic blockade of cell division generates animals with oversized periderm cells, yet, unexpectedly, development to adulthood is not impaired. Our findings reveal stage-dependent differential responsiveness to ERK signaling and marked developmental robustness in growing teleost skin.

Article Details

Volume / Issue Vol. 122, Issue 10
Published March 11, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (9)

N

Nitya Ramkumar

Department of Cell Biology, Duke University Medical Center

C

Christian Richardson

Department of Cell Biology, Duke University Medical Center

M

Makinnon O'Brien

Department of Cell Biology, Duke University Medical Center

F

Faraz Ahmed Butt

Department of Cell Biology, Duke University Medical Center

J

Jieun Park

A

Anna T. Chao

Department of Cell Biology, Duke University Medical Center

M

Michel Bagnat

Department of Cell Biology, Duke University Medical Center

K

Kenneth D. Poss

S

Stefano Di Talia