Overexpression of potassium channel Kcna5 alters skeletal patterning in the zebrafish regenerating fin

Skeletal patterning relies on a complex network of molecular and genetic regulators. However, our understanding of pathways governing joint placement and morphogenesis remains incomplete. Prior studies have demonstrated that medially located Cx43 mediated gap junctional intercellular communication (GJIC) inhibits joint formation by the adjacent lateral skeletal precursor cells, and thereby determines skeletal patterning in the teleost regenerating fin. Here, we test the model that Cx43-GJIC regulates joint formation by propagating changes in membrane potential (ΔV<sub>m</sub>). To provide evidence that ΔV<sub>m</sub> is sufficient to influence joint formation, we generated a transgenic line that expresses the X. laevis voltage-gated channel, shaker-related subfamily, member 5 (kcna5) behind the temperature-inducible heat shock protein 70 (hsp70) promoter. Using this line, we demonstrate that Xl-kcna5 overexpression delays evx1 expression and causes longer segments. Moreover, the increased segment length in response to Xl-Kcna5 overexpression requires Cx43. These findings support a model whereby potassium channels act together with gap junction channels to influence joint formation, and therefore skeletal patterning, in the zebrafish regenerating fin.

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Publication Details

Journal
Developmental Biology
Published
2025-09-03
DOI
https://doi.org/10.1016/j.ydbio.2025.09.001
Primary Topic
Developmental Biology and Gene Regulation
Type
article
Field-Weighted Citation Impact
0.00

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article

Overexpression of potassium channel Kcna5 alters skeletal patterning in the zebrafish regenerating fin

Xinxhao Li, M. Kathryn Iovine, Alexander W. Seaver
Developmental Biology
Developmental Biology and Gene Regulation
article

Overexpression of potassium channel Kcna5 alters skeletal patterning in the zebrafish regenerating fin

Xinxhao Li, M. Kathryn Iovine, Alexander W. Seaver
article en

Abstract

Skeletal patterning relies on a complex network of molecular and genetic regulators. However, our understanding of pathways governing joint placement and morphogenesis remains incomplete. Prior studies have demonstrated that medially located Cx43 mediated gap junctional intercellular communication (GJIC) inhibits joint formation by the adjacent lateral skeletal precursor cells, and thereby determines skeletal patterning in the teleost regenerating fin. Here, we test the model that Cx43-GJIC regulates joint formation by propagating changes in membrane potential (ΔV<sub>m</sub>). To provide evidence that ΔV<sub>m</sub> is sufficient to influence joint formation, we generated a transgenic line that expresses the X. laevis voltage-gated channel, shaker-related subfamily, member 5 (kcna5) behind the temperature-inducible heat shock protein 70 (hsp70) promoter. Using this line, we demonstrate that Xl-kcna5 overexpression delays evx1 expression and causes longer segments. Moreover, the increased segment length in response to Xl-Kcna5 overexpression requires Cx43. These findings support a model whereby potassium channels act together with gap junction channels to influence joint formation, and therefore skeletal patterning, in the zebrafish regenerating fin.

Developmental BiologyVol. 528
Lehigh University, National Institutes of Health, Eunice Kennedy Shriver National Institute of Child Health and Human Development
Openalex Percentile: Top 79%
Developmental Biology and Gene Regulation
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