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  <front>
    <journal-meta>
      <journal-id journal-id-type="publisher-id">JE</journal-id>
      <journal-title-group>
        <journal-title>Journal of Embryology</journal-title>
      </journal-title-group>
      <issn pub-type="epub">3070-5657</issn>
      <publisher>
        <publisher-name>Open Access Pub</publisher-name>
        <publisher-loc>United States</publisher-loc>
      </publisher>
    </journal-meta>
    <article-meta>
      <article-id pub-id-type="doi">10.14302/issn.3070-5657.je-17-1638</article-id>
      <article-id pub-id-type="publisher-id">JE-17-1638</article-id>
      <article-categories>
        <subj-group>
          <subject>research-article</subject>
        </subj-group>
      </article-categories>
      <title-group>
        <article-title>Development of the Hand</article-title>
      </title-group>
      <contrib-group>
        <contrib contrib-type="author">
          <name>
            <surname>Baykal</surname>
            <given-names>B</given-names>
          </name>
          <xref ref-type="aff" rid="idm1849621876">1</xref>
          <xref ref-type="aff" rid="idm1849620580">*</xref>
        </contrib>
        <contrib contrib-type="author">
          <name>
            <surname>Turkkan</surname>
            <given-names>S</given-names>
          </name>
          <xref ref-type="aff" rid="idm1849621516">2</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1849621876">
        <label>1</label>
        <addr-line>Department of Histology and Embryology, Gulhane Medical Faculty, University of Health Sciences, Ankara, Turkey</addr-line>
      </aff>
      <aff id="idm1849621516">
        <label>2</label>
        <addr-line>Department of Hand Surgery, Gulhane Research and Training Hospital, University of Health Sciences, Ankara, Turkey</addr-line>
      </aff>
      <aff id="idm1849620580">
        <label>*</label>
        <addr-line>Corresponding author</addr-line>
      </aff>
      <contrib-group>
        <contrib contrib-type="editor">
          <name>
            <surname>Jianliang</surname>
            <given-names>jin</given-names>
          </name>
          <xref ref-type="aff" rid="idm1849473060">1</xref>
        </contrib>
      </contrib-group>
      <aff id="idm1849473060">
        <label>1</label>
        <addr-line>Department of Anatomy, School of Basic Medicine, Nanjing Medical University</addr-line>
      </aff>
      <author-notes>
        <corresp>
    
    Baykal B, <addr-line>Department of Histology and Embryology, Gulhane Medical Faculty, University of Health Sciences, Ankara, Turkey</addr-line>,  Email: <email>baris_baykal@yahoo.com</email></corresp>
        <fn fn-type="conflict" id="idm1842463788">
          <p>The authors have declared that no competing interests exist.</p>
        </fn>
      </author-notes>
      <pub-date pub-type="epub" iso-8601-date="2017-05-17">
        <day>17</day>
        <month>05</month>
        <year>2017</year>
      </pub-date>
      <volume>1</volume>
      <issue>1</issue>
      <fpage>01</fpage>
      <lpage>05</lpage>
      <history>
        <date date-type="received">
          <day>02</day>
          <month>06</month>
          <year>2017</year>
        </date>
        <date date-type="accepted">
          <day>21</day>
          <month>08</month>
          <year>2017</year>
        </date>
        <date date-type="online">
          <day>13</day>
          <month>09</month>
          <year>2017</year>
        </date>
      </history>
      <permissions>
        <copyright-statement>©  </copyright-statement>
        <copyright-year>2017</copyright-year>
        <copyright-holder>Baris Baykal, et al</copyright-holder>
        <license xlink:href="http://creativecommons.org/licenses/by/4.0/" xlink:type="simple">
          <license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.</license-p>
        </license>
      </permissions>
      <self-uri xlink:href="http://openaccesspub.org/je/article/467">This article is available from http://openaccesspub.org/je/article/467</self-uri>
      <abstract>
        <p>Development of the hand occurs as a complex series of events. In order to understand the mechanisms of developmental hand anomalies, the clinician has to understand the normal embryonic development of the hand. In this review, we present the development of the hand in the light of new literature knowledge.</p>
      </abstract>
      <kwd-group>
        <kwd>Development hand anomalies</kwd>
      </kwd-group>
      <counts>
        <fig-count count="1"/>
        <table-count count="0"/>
        <page-count count="5"/>
      </counts>
    </article-meta>
  </front>
  <body>
    <sec id="idm1849471548" sec-type="intro">
      <title>Introduction</title>
      <p>The development of the hand depends on many regulatory molecules secreted by varios regions of the developing upper limb. While some of these molecules have stimulatory effects, others have inhibitory effects. Both proliferation and apoptosis take place in various areas of the developing upper limb in order to form skeletal stuctures and spaces. The development of upper extremity has to be understood in order to understand the development of the hand. Being aware of the development and developmental mechanisms of the hand, may help clinicians in understanding the underlying mechanisms of congenital hand malformations.</p>
    </sec>
    <sec id="idm1849469964">
      <title>Development of the Upper Extremıty</title>
      <p>Development of the upper extremity begins with the appearance of the upper extremity bud by means of high levels of proliferation in the lower five cervical and first thoracal myotomes of somatopleural mesenchyme due to the effects of fibroblast growth factor 10 (FGF-10) and T-box transcription factor (Tbx5) on the 27. day of intrauterine life <xref ref-type="bibr" rid="ridm1841720548">1</xref><xref ref-type="bibr" rid="ridm1841788812">2</xref><xref ref-type="bibr" rid="ridm1841826252">3</xref><xref ref-type="bibr" rid="ridm1841792412">4</xref>. Specialized signaling centers that express and secrete many molecules help in determining and development along three spatial limb axes: proximodistal, anteroposterior, and dorsoventral <xref ref-type="bibr" rid="ridm1841580972">5</xref>. Three specialized signaling centers occur within the growing limb bud: apical ectodermal ridge, zone of polarizing activity, and nonridge ectoderm <xref ref-type="bibr" rid="ridm1841580972">5</xref>.</p>
      <p>A condensed mesenchyme exists in the center of the extremity bud and a ridge termed as apical ectodermal ridge composed of tall columnar epithelium is present on the apical edge of the extremity bud <xref ref-type="bibr" rid="ridm1841720548">1</xref><xref ref-type="bibr" rid="ridm1841788812">2</xref>. The location of the apical ectodermal ridge is determined by radical fringe and engrailed-1 molecules secreted from the dorsal ecdoderm and ventral ectoderm of the extremity bud, respectively <xref ref-type="bibr" rid="ridm1841826252">3</xref>. While apical ectodermal ridge orchestrates the development of the extremity bud <xref ref-type="bibr" rid="ridm1841788812">2</xref>, the mesenchyme induces and maintains the development of the apical ectodermal ridge <xref ref-type="bibr" rid="ridm1841720548">1</xref><xref ref-type="bibr" rid="ridm1841576076">6</xref>. Fibroblast growth factors 4, 9 and 17 (FGF-4, FGF-9 and FGF-17) expressed by the apical ectodermal ridge induces outgrowth of the bud <xref ref-type="bibr" rid="ridm1841826252">3</xref><xref ref-type="bibr" rid="ridm1841576076">6</xref>. </p>
      <p>In the guidance of homeobox b8 (Hoxb8), which exists at high concentrations at the posterior edge of the extremity bud <xref ref-type="bibr" rid="ridm1841826252">3</xref>, mesenchymal cells aggregate forming the zone of polarizing activity <xref ref-type="bibr" rid="ridm1841788812">2</xref><xref ref-type="bibr" rid="ridm1841576076">6</xref><xref ref-type="bibr" rid="ridm1841572044">7</xref>. The principal zone that controls the development of the extremities along their anteroposterior axes at a normal pattern with sonic hedgehog it secretes <xref ref-type="bibr" rid="ridm1841826252">3</xref> is the zone of polarizing activity <xref ref-type="bibr" rid="ridm1841788812">2</xref><xref ref-type="bibr" rid="ridm1841572044">7</xref>. Gremlin, which is expressed in a domain anterior to the zone of polarizing activity <xref ref-type="bibr" rid="ridm1841567292">8</xref> maintains the apical ectodermal ridge <xref ref-type="bibr" rid="ridm1841788812">2</xref> and helps determine the anteroposterior axis of the bud <xref ref-type="bibr" rid="ridm1841826252">3</xref>. Sonic hedgehod also acts in the maintenance of the structure and functions of the apical ectodermal ridge <xref ref-type="bibr" rid="ridm1841826252">3</xref><xref ref-type="bibr" rid="ridm1841576076">6</xref>. </p>
    </sec>
    <sec id="idm1849471692">
      <title>Development of the Hand</title>
      <p>The development of the hand begins with the flattening of the distal ends of the extremity buds on the 34-38th days of development. Thus, paddle-like hand plates occur <xref ref-type="bibr" rid="ridm1841720548">1</xref><xref ref-type="bibr" rid="ridm1841788812">2</xref>. Development of the digits begin with the fragmentation of apical ectodermal ridge and on the 46th day of development hand plates take a notched shape and digit rays form <xref ref-type="bibr" rid="ridm1841792412">4</xref>. Apical ectodermal ridges at the tips of each digit, induces the mesenchyme to condense and transform into the primordia of phalanges <xref ref-type="bibr" rid="ridm1841572044">7</xref>. As a result of this induction cartilaginous primordia is formed. Transforming growth factor beta proteins (TGFB’s) and activins play a specific role in the induction of chondrogenesis in the digit ray <xref ref-type="bibr" rid="ridm1841541644">9</xref><xref ref-type="bibr" rid="ridm1841540420">10</xref><xref ref-type="bibr" rid="ridm1841526236">11</xref>. Bone morphogenic proteins (BMP’s) have reciprocal effects in this process. They have both growth promoter <xref ref-type="bibr" rid="ridm1841567292">8</xref> and apoptotic effects <xref ref-type="bibr" rid="ridm1841522996">12</xref> and the effects seem to take place by the changes in receptor expressions <xref ref-type="bibr" rid="ridm1841518676">13</xref>. The chondrogenic effects of BMP’s are enhancement of cell adhesion between the cell clusters in the regions of chondrogenesis, increasing of expression of Sry-related HMG box (SOX) genes and matrix production <xref ref-type="bibr" rid="ridm1841518676">13</xref>. SOX9 expression is the first indicator of verging towards chondrogenesis (<xref ref-type="fig" rid="idm1841705676">Figure 1</xref>) <xref ref-type="bibr" rid="ridm1841518676">13</xref><xref ref-type="bibr" rid="ridm1841533724">14</xref>. </p>
      <fig id="idm1841705676">
        <label>Figure 1.</label>
        <caption>
          <title> Diagram showing the apical ectodermal ridge, areas of cartilage matrix production due to the expression of SOX9, and the areas where apoptosis occurs by the effect of BMP-2, BMP-4, BMP-7, Msx-1 and Msx-2 in a developing digit. (Modified from “Tina V. Hellmann, Joachim Nickel and Thomas D. Mueller (2012). Missense Mutations in GDF-5 Signaling: Molecular Mechanisms Behind Skeletal Malformation, Mutations in Human Genetic Disease, Prof. David Cooper (Ed.), InTech, DOI: 10.5772/35195. OPEN ACCESS”)</title>
        </caption>
        <graphic xlink:href="images/image1.jpg" mime-subtype="jpg"/>
      </fig>
      <p>The extracellular matrix plays important roles in chondrogenesis. First of all, it acts as a scaffold for cell aggregation. It possibly effects the local transmission of growth factors both temporally and in concentration gradients. The extracellular matrix components themselves also are present in the developing digital ray at different concentrations. For example, a proteoglycan, syndecan-3, is expressed at high levels restricted to perichondrium in the cell aggregate before chondrogenesis and in the developing joints after differentiation <xref ref-type="bibr" rid="ridm1841529692">15</xref><xref ref-type="bibr" rid="ridm1841486084">16</xref>.</p>
      <p>Spesific phalangeal segments arise as a result of segmentation <xref ref-type="bibr" rid="ridm1841826252">3</xref>. Activin-Like Kinase 3 (ALK3), a BMP receptor, may play a key regulatory role in joint formation and interdigitation via apoptosis <xref ref-type="bibr" rid="ridm1841483420">17</xref>. At the 50th day, the digits are webbed <xref ref-type="bibr" rid="ridm1841792412">4</xref>. The loose mesenchyme between the digit ray undergoes tissue breakdown via apoptosis and at the 52nd day seperate digits form <xref ref-type="bibr" rid="ridm1841792412">4</xref><xref ref-type="bibr" rid="ridm1841572044">7</xref>. BMP-2, BMP-4, BMP-7, Muscle Segment Homeobox 1 and 2 (Msx-1 and Msx-2) expressed in interdigital areas are the molecules that play a role in interdigital cell death <xref ref-type="bibr" rid="ridm1841826252">3</xref>. Sonic hedgehog (shh) is the molecule that plays the main role in the determination of digit identity <xref ref-type="bibr" rid="ridm1841826252">3</xref> and the formation of digit patterning <xref ref-type="bibr" rid="ridm1841788812">2</xref>. Ossification of the phalanges occur antenatally. Carpal bones ossify postnatally <xref ref-type="bibr" rid="ridm1841478812">18</xref>. </p>
      <p>The muscles of the hand are thought to develop in situ not by migration <xref ref-type="bibr" rid="ridm1841493500">19</xref><xref ref-type="bibr" rid="ridm1841489324">20</xref>. Initially, the mesenchyme of the hand divides into superficial and deep layers. Three muscle primordia (radial, middle and ulnar) develop from the superficial layer. Abductor pollicis brevis, flexor digitorum superficialis and abductor digiti minimi muscles develop from these primordia, respectively.  The deep layer gives rise to interosseous and contrahentes muscles. The latter develops into the adductor pollicis muscle <xref ref-type="bibr" rid="ridm1841489324">20</xref>. Tendons, synovial sheets and pulley system of the digits are observed as condensing mesencyme at the 9th week of development. At the 12th week pulleys are identifiable as in the adult <xref ref-type="bibr" rid="ridm1841457252">21</xref>. </p>
      <p>Brachial artery reaches the palm at 16 mm embryo stage. Digital arteries originate from the regressing capillary nets during notching. A digital vessel forms on the two sides of each forming interspace <xref ref-type="bibr" rid="ridm1841456316">22</xref>. Cells that originate and migrate from the neural crest contribute to the formation of the nerves of the limbs <xref ref-type="bibr" rid="ridm1841572044">7</xref>. Nerves begin grow into the limb bud at approximately 36th day of development <xref ref-type="bibr" rid="ridm1841580972">5</xref>.</p>
    </sec>
    <sec id="idm1849467732">
      <title>Conclusıon</title>
      <p>Development of the hand occurs in a complex manner by various molecular interactions. The awareness of hand development may help in understanding the formation mechanisms of congenital hand anomalies. </p>
    </sec>
  </body>
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