Hostname: page-component-8448b6f56d-m8qmq Total loading time: 0 Render date: 2024-04-24T15:28:11.324Z Has data issue: false hasContentIssue false

Active ion transport mechanisms and their role for past, present and future life in marine systems

Published online by Cambridge University Press:  05 May 2020

Marian Y. Hu*
Affiliation:
Institute of Physiology, Christian-Albrechts-Universität zu Kiel, Hermann-Rodewaldstr. 5 24118Kiel, Germany
*
Author for correspondence: Marian Y. Hu, E-mail: m.hu@physiologie.uni-kiel.de
Rights & Permissions [Opens in a new window]

Abstract

Type
Editorial
Copyright
Copyright © Marine Biological Association of the United Kingdom 2020

Homoeostatic regulation of biological compartments was a critical step in the evolution of life on earth. Only in a confined space with controlled abiotic conditions, can chemical processes take place in a reproducible manner, leading to the origin of biochemical interactions between lipids, enzymes and nucleic acids. Some hypotheses identify that proton translocating proteins were among the first transporters in the evolution of the cell by using environmental ion and pH gradients to generate phosphate-based energy equivalents (Weiss et al., Reference Weiss, Sousa, Mrnjavac, Neukirchen, Roettger, Nelson-Sathi and Martin2016). This central importance of proton translocating mechanisms is reflected in the ubiquitous existence of V- and F-type ATPases in all organisms on earth, ranging from eukaryotes to bacteria and archaea (Mulkijjanian et al., Reference Mulkijjanian, Marakova, Galperin and Koonin2007; Grüber et al., Reference Grüber, Manimekalai, Mayer and Müller2014). Due to the necessity to optimally regulate biological compartments for the functioning of enzymes, a wide range of ion-transporting proteins have evolved to regulate intra- and extra-cellular homoeostasis. In addition, primary active ion transport by ATPases is not only capable of generating ion concentration differences but are mostly associated with a net flux of electrical charges, leading to the generation of an electrical potential across biological membranes. This electrical potential is responsible for the excitability of cells (e.g. nerve and muscle cells), and together with the chemical gradient driving all secondary active transport processes, essential for ionic homoeostasis and nutrition.

Comparative approaches through studying organisms from different positions in the tree of life can provide insights into the evolutionary diversity as well as the common origin of ion-transport mechanisms. Here molecular advances providing genomes and transcriptomes have opened new venues for the identification of ion pumps in animals, plants and microbes. However, besides this access to genetic information, allowing reconstructions of evolutionary processes, mechanistic knowledge regarding the physiological function of these ion pumps remains of fundamental importance. This becomes particularly evident given the fact that selection acts on the functionality (e.g. salinity and pH tolerance, water homoeostasis) of an organism in a particular environment, leading to changes in the genetic material and not vice versa. Thus, understanding the mechanisms underlying homoeostatic regulation represents fundamental information that, together with genomic approaches can lead to a holistic understanding of the function and evolution of membrane transport processes. Along these lines, the Journal of the Marine Biological Association of the United Kingdom (JMBA) has promoted research in the field of ion-transport and homoeostatic regulation in marine organisms since the first issue in 1889 that included an article on the function of the electrical organ of skates (Sanderson & Gotch, Reference Sanderson and Gotch1889). Electrical organs are found in several fish species and are believed to serve communication and feeding purposes, representing a prime example of cellular ion transport. Electrical organs are capable of generating high voltages based on the same electrophysiological principles as found in the action potential of nerve and muscle cells using the electrochemical gradients provided by the Na+/K+-ATPase (Bennett, Reference Bennett1970). Over the last century JMBA has published a large number of studies addressing the ion-transport physiology of aquatic organisms including crustaceans (Panikkar, Reference Panikkar1941; Wheatly, Reference Wheatly1997), molluscs (Stallworthy, Reference Stallworthy1970; Clarke et al., Reference Clarke, Denton and Gilpin-Brown1979) and fish (Wood & Shuttleworth, Reference Wood and Shuttleworth1996), to name just a few.

Studying membrane transport processes for the regulation of intracellular and extracellular homoeostasis is a core discipline in environmental physiology. In the marine environment homoeostatic regulation plays a pivotal role in allowing organisms to occupy ecological niches in diverse marine habitats ranging from the poles to the tropics and from coastal areas to the deep sea, including the hydrothermal vent systems of mid ocean ridges (Somero et al., Reference Somero, Lockwood and Tomanek2017). Here ion-regulatory mechanisms represent a key trait that allowed marine organisms to survive in environments with strong fluctuations in salinity or pH, such as coastal areas and estuaries. The characterization of these physiological adaptations helps to illuminate adaptive strategies to specific environments and also provides a glimpse into the future as to how animals may respond to changes in marine systems (Melzner et al., Reference Melzner, Mark, Seibel and Tomanek2020). In the context of climate change, the physiology of homoeostatic regulation in marine organisms has received considerable attention from the research community. Changes in seawater salinity and pH are key factors driven by the global phenomenon of climate change that directly challenges homoeostatic regulation of marine species. In particular, pH regulatory systems have been identified as an important physiological trait associated with a range of important functions in marine organisms including blood-gas transport, digestion and biomineralization (Stumpp et al., Reference Stumpp, Hu, Melzner, Gutowska, Dorey, Himmerkus, Holtmann, Dupont, Thorndyke and Bleich2012, Reference Stumpp, Hu, Casties, Saborowski, Bleich, Melzner and Dupont2013; Hu et al., Reference Hu, Lee, Stumpp, Guh, Hwang and Tseng2014). The importance of ion-regulatory processes in the resilience of marine species to changes in seawater pH has been underlined by studies addressing the potential of organisms to evolutionarily adapt to near-future ocean acidification. These studies demonstrate an increased selection pressure, seen in higher single nucleotide polymorphisms (SNPs), on genes coding for ion-regulatory and metabolic proteins in sea urchin larvae raised under near-future ocean acidification conditions (Pespeni et al., Reference Pespeni, Sanford, Gaylord, Hill, Hosfeld, Jaris, LaVigne, Lenz, Russell, Young and Palumbi2013).

Homoeostatic regulation in organisms is a foundation for life that has led to the evolution of an enormous diversity of ion pumps, transporters and channels. Based on phylogenetic position, a higher or lower complexity of these membrane proteins work in concert to secure homoeostasis in organisms allowing them to occupy different ecological niches. Thus, to generate a holistic understanding of the fundamental process of homoeostatic regulation in organisms, an integrative approach, including ecology, physiology and molecular biology is necessary. In this way, connecting the concept of homoeostasis from the ecosystem through to the molecular level will help in understanding the role of ion-regulatory strategies in organisms of past, present and future oceans.

References

Bennett, MVL (1970) Comparative physiology: electric organs. Annual Review of Physiology 32, 471528.CrossRefGoogle ScholarPubMed
Clarke, MR, Denton, EJ and Gilpin-Brown, JB (1979) On the use of ammonium for buoyancy in squids. Journal of the Marine Biological Association of the United Kingdom 59, 259276.CrossRefGoogle Scholar
Grüber, G, Manimekalai, MSS, Mayer, F and Müller, V (2014) ATP synthase from arcaea: the beauty of a molecular motor. Biochimica Biophysica Acta – Bioenergetics 1837, 940952.CrossRefGoogle ScholarPubMed
Hu, MY, Lee, J-R, Stumpp, M, Guh, YJ, Hwang, PP and Tseng, Y-C (2014) Branchial NH4+-dependent acid-base transport mechanisms and energy metabolism of squid (Sepioteuthis lessoniana) affected by seawater acidification. Frontiers in Zoology 11, 55.Google Scholar
Melzner, F, Mark, CF, Seibel, BA and Tomanek, L (2020) Ocean acidification and coastal marine invertebrates: tracking CO2 effects from seawater to the cell. Annual Review of Marine Science 12, 499523.CrossRefGoogle ScholarPubMed
Mulkijjanian, AY, Marakova, KS, Galperin, MY and Koonin, EV (2007) Inventing the dynamo machine: the evolution of the F-type and V-type ATPases. Nature Reviews Microbiology 5, 892899.CrossRefGoogle Scholar
Panikkar, NK (1941) Osmoregulation in some palaemonid prawns. Journal of the Marine Biological Association of the United Kingdom 25, 317359.CrossRefGoogle Scholar
Pespeni, MH, Sanford, E, Gaylord, B, Hill, TM, Hosfeld, JD, Jaris, HK, LaVigne, M, Lenz, EA, Russell, AD, Young, MK and Palumbi, SR (2013) Evolutionary change during experimental ocean acidification. Proceedings of the National Academy of Sciences USA 110, 69376942.CrossRefGoogle ScholarPubMed
Sanderson, B and Gotch, F (1889) Further investigations on the function of the electrical organ of the skate. Journal of the Marine Biological Association of the United Kingdom 1, 7474.CrossRefGoogle Scholar
Somero, GN, Lockwood, BL and Tomanek, L (2017) Biochemical Adaptation: Responses to Environmental Challenges from Life´s Origins to the Anthropocene. Sunderland, MA: Sinauer Associates.Google Scholar
Stallworthy, WB (1970) Electro-osmosis in squid axons. Journal of the Marine Biological Association of the United Kingdom 50, 349363.CrossRefGoogle Scholar
Stumpp, M, Hu, MY, Melzner, F, Gutowska, MA, Dorey, N, Himmerkus, N, Holtmann, WC, Dupont, ST, Thorndyke, MC and Bleich, M (2012) Acidified seawater impacts sea urchin larvae pH regulatory systems relevant for calcification. Proceedings of the National Academy of Sciences USA 109, 1819218197.CrossRefGoogle ScholarPubMed
Stumpp, M, Hu, MY, Casties, I, Saborowski, R, Bleich, M, Melzner, F and Dupont, ST (2013) Digestion in sea urchin larvae impaired under ocean acidification. Nature Climate Change 3, 1044.CrossRefGoogle Scholar
Weiss, MC, Sousa, FL, Mrnjavac, N, Neukirchen, S, Roettger, M, Nelson-Sathi, S and Martin, WF (2016) The physiology and habitat of the last universal common ancestor. Nature Microbiology 1, 16116.CrossRefGoogle ScholarPubMed
Wheatly, MG (1997) Crustacean models for studying calcium transport: the journey from whole organisms to molecular mechanisms. Journal of the Marine Biological Association of the United Kingdom 77, 107125.CrossRefGoogle Scholar
Wood, CM and Shuttleworth, TJ (1996) Cellular and Molecular Approaches to Fish Ionic Regulation. San Diego, CA: Cambridge University Press.Google Scholar